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Compile Data Set for Download or QSAR

Found 53 hits Enz. Inhib. hit(s) with all data for entry = 50001353   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kJ/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Glucagon-like peptide 1 receptor


(Homo sapiens (Human))
BDBM50277053
PNG
(CHEMBL4174382)
Show SMILES CSCC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CO)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CS)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)Cc1cnc[nH]1)[C@@H](C)O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(N)=O |r|
Show InChI InChI=1S/C150H220N44O48S2/c1-70(2)50-94(131(225)174-93(45-49-244-9)130(224)181-100(57-112(156)207)140(234)193-118(73(6)199)121(157)215)176-134(228)99(55-80-61-165-86-27-17-16-26-84(80)86)180-129(223)92(41-44-111(155)206)175-146(240)117(71(3)4)192-138(232)97(51-76-22-12-10-13-23-76)179-135(229)101(58-114(209)210)182-128(222)91(40-43-110(154)205)169-122(216)72(5)168-125(219)88(29-20-47-163-149(158)159)170-126(220)89(30-21-48-164-150(160)161)172-143(237)106(66-197)188-137(231)103(60-116(213)214)184-145(239)108(68-243)190-133(227)96(54-79-33-37-83(203)38-34-79)177-127(221)87(28-18-19-46-151)171-142(236)105(65-196)187-132(226)95(53-78-31-35-82(202)36-32-78)178-136(230)102(59-115(211)212)183-144(238)107(67-198)189-148(242)120(75(8)201)194-139(233)98(52-77-24-14-11-15-25-77)185-147(241)119(74(7)200)191-113(208)63-166-124(218)90(39-42-109(153)204)173-141(235)104(64-195)186-123(217)85(152)56-81-62-162-69-167-81/h10-17,22-27,31-38,61-62,69-75,85,87-108,117-120,165,195-203,243H,18-21,28-30,39-60,63-68,151-152H2,1-9H3,(H2,153,204)(H2,154,205)(H2,155,206)(H2,156,207)(H2,157,215)(H,162,167)(H,166,218)(H,168,219)(H,169,216)(H,170,220)(H,171,236)(H,172,237)(H,173,235)(H,174,225)(H,175,240)(H,176,228)(H,177,221)(H,178,230)(H,179,229)(H,180,223)(H,181,224)(H,182,222)(H,183,238)(H,184,239)(H,185,241)(H,186,217)(H,187,226)(H,188,231)(H,189,242)(H,190,227)(H,191,208)(H,192,232)(H,193,234)(H,194,233)(H,209,210)(H,211,212)(H,213,214)(H4,158,159,163)(H4,160,161,164)/t72-,73+,74+,75+,85-,87-,88-,89-,90-,91-,92-,93-,94-,95-,96-,97-,98-,99-,100-,101-,102-,103-,104-,105-,106-,107-,108-,117-,118-,119-,120-/m0/s1
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
KEGG
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 5.90n/an/an/an/a



China Pharmaceutical University

Curated by ChEMBL


Assay Description
Agonist activity at full length human GLP1R expressed in HEK293 cells assessed as increase in cAMP accumulation after 20 mins by HTRF assay


Eur J Med Chem 138: 1158-1169 (2017)


Article DOI: 10.1016/j.ejmech.2017.07.046
BindingDB Entry DOI: 10.7270/Q2QC061V
More data for this
Ligand-Target Pair
Glucagon receptor


(Homo sapiens (Human))
BDBM50277058
PNG
(CHEMBL4165144)
Show SMILES CSCC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CSC1CC(=O)N(CCCCCCCCCCCC(O)=O)C1=O)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CO)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)Cc1cnc[nH]1)[C@@H](C)O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(N)=O |r|
Show InChI InChI=1S/C169H251N45O52S2/c1-84(2)62-108(148(247)192-107(56-61-267-10)147(246)200-115(70-128(175)227)158(257)212-136(87(7)219)139(176)238)195-152(251)114(68-94-75-184-100-37-26-25-36-98(94)100)199-146(245)106(52-55-127(174)226)193-164(263)135(86(5)6)211-156(255)112(64-90-32-20-18-21-33-90)198-153(252)116(71-132(232)233)201-145(244)105(51-54-126(173)225)191-163(262)123(82-268-124-74-130(229)214(167(124)266)60-29-17-15-13-11-12-14-16-24-41-131(230)231)209-144(243)103(40-31-59-183-169(179)180)187-142(241)102(39-30-58-182-168(177)178)189-161(260)121(80-217)207-155(254)118(73-134(236)237)202-149(248)109(63-85(3)4)194-150(249)110(66-92-42-46-96(222)47-43-92)196-143(242)101(38-27-28-57-170)188-160(259)120(79-216)206-151(250)111(67-93-44-48-97(223)49-45-93)197-154(253)117(72-133(234)235)203-162(261)122(81-218)208-166(265)138(89(9)221)213-157(256)113(65-91-34-22-19-23-35-91)204-165(264)137(88(8)220)210-129(228)77-185-141(240)104(50-53-125(172)224)190-159(258)119(78-215)205-140(239)99(171)69-95-76-181-83-186-95/h18-23,25-26,32-37,42-49,75-76,83-89,99,101-124,135-138,184,215-223H,11-17,24,27-31,38-41,50-74,77-82,170-171H2,1-10H3,(H2,172,224)(H2,173,225)(H2,174,226)(H2,175,227)(H2,176,238)(H,181,186)(H,185,240)(H,187,241)(H,188,259)(H,189,260)(H,190,258)(H,191,262)(H,192,247)(H,193,263)(H,194,249)(H,195,251)(H,196,242)(H,197,253)(H,198,252)(H,199,245)(H,200,246)(H,201,244)(H,202,248)(H,203,261)(H,204,264)(H,205,239)(H,206,250)(H,207,254)(H,208,265)(H,209,243)(H,210,228)(H,211,255)(H,212,257)(H,213,256)(H,230,231)(H,232,233)(H,234,235)(H,236,237)(H4,177,178,182)(H4,179,180,183)/t87-,88-,89-,99+,101+,102+,103+,104+,105+,106+,107+,108+,109+,110+,111+,112+,113+,114+,115+,116+,117+,118+,119+,120+,121+,122+,123+,124?,135+,136+,137+,138+/m1/s1
PDB
MMDB

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 4.40n/an/an/an/a



China Pharmaceutical University

Curated by ChEMBL


Assay Description
Agonist activity at human GCGR expressed in HEK293 cells assessed as increase in cAMP accumulation after 20 mins by HTRF assay


Eur J Med Chem 138: 1158-1169 (2017)


Article DOI: 10.1016/j.ejmech.2017.07.046
BindingDB Entry DOI: 10.7270/Q2QC061V
More data for this
Ligand-Target Pair
Glucagon receptor


(Homo sapiens (Human))
BDBM50277055
PNG
(CHEMBL4169653)
Show SMILES CCCCCCCCCCCCN1C(=O)CC(SC[C@H](NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)Cc2cnc[nH]2)[C@@H](C)O)[C@@H](C)O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](Cc2ccccc2)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](Cc2c[nH]c3ccccc23)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(N)=O)C1=O |r|
Show InChI InChI=1S/C169H253N45O49S2/c1-13-14-15-16-17-18-19-20-21-32-62-214-131(228)76-125(167(214)263)265-83-124(163(259)191-105(43-34-61-183-169(179)180)144(240)189-104(42-33-60-182-168(177)178)143(239)187-88(8)140(236)188-107(53-56-127(173)224)146(242)202-118(73-132(229)230)154(250)199-114(66-92-35-24-22-25-36-92)157(253)211-135(87(6)7)164(260)194-108(54-57-128(174)225)147(243)200-116(70-96-77-184-102-40-29-28-39-100(96)102)153(249)196-110(64-85(2)3)149(245)193-109(58-63-264-12)148(244)201-117(72-129(175)226)159(255)212-136(89(9)218)139(176)235)209-156(252)120(75-134(233)234)203-150(246)111(65-86(4)5)195-151(247)112(68-94-44-48-98(221)49-45-94)197-145(241)103(41-30-31-59-170)190-161(257)122(81-216)207-152(248)113(69-95-46-50-99(222)51-47-95)198-155(251)119(74-133(231)232)204-162(258)123(82-217)208-166(262)138(91(11)220)213-158(254)115(67-93-37-26-23-27-38-93)205-165(261)137(90(10)219)210-130(227)79-185-142(238)106(52-55-126(172)223)192-160(256)121(80-215)206-141(237)101(171)71-97-78-181-84-186-97/h22-29,35-40,44-51,77-78,84-91,101,103-125,135-138,184,215-222H,13-21,30-34,41-43,52-76,79-83,170-171H2,1-12H3,(H2,172,223)(H2,173,224)(H2,174,225)(H2,175,226)(H2,176,235)(H,181,186)(H,185,238)(H,187,239)(H,188,236)(H,189,240)(H,190,257)(H,191,259)(H,192,256)(H,193,245)(H,194,260)(H,195,247)(H,196,249)(H,197,241)(H,198,251)(H,199,250)(H,200,243)(H,201,244)(H,202,242)(H,203,246)(H,204,258)(H,205,261)(H,206,237)(H,207,248)(H,208,262)(H,209,252)(H,210,227)(H,211,253)(H,212,255)(H,213,254)(H,229,230)(H,231,232)(H,233,234)(H4,177,178,182)(H4,179,180,183)/t88-,89+,90+,91+,101-,103-,104-,105-,106-,107-,108-,109-,110-,111-,112-,113-,114-,115-,116-,117-,118-,119-,120-,121-,122-,123-,124-,125?,135-,136-,137-,138-/m0/s1
PDB
MMDB

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 2.40n/an/an/an/a



China Pharmaceutical University

Curated by ChEMBL


Assay Description
Agonist activity at human GCGR expressed in HEK293 cells assessed as increase in cAMP accumulation after 20 mins by HTRF assay


Eur J Med Chem 138: 1158-1169 (2017)


Article DOI: 10.1016/j.ejmech.2017.07.046
BindingDB Entry DOI: 10.7270/Q2QC061V
More data for this
Ligand-Target Pair
Glucagon receptor


(Homo sapiens (Human))
BDBM50277056
PNG
(CHEMBL4163714)
Show SMILES CSCC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CO)NC(=O)[C@H](CS)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)Cc1cnc[nH]1)[C@@H](C)O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(N)=O |r|
Show InChI InChI=1S/C152H226N44O46S2/c1-72(2)52-97(133(225)176-96(47-51-244-11)132(224)184-104(60-115(158)209)142(234)195-120(76(8)201)123(159)215)179-137(229)103(58-83-63-167-89-29-19-18-28-87(83)89)183-131(223)95(43-46-114(157)208)177-148(240)119(74(5)6)194-140(232)101(54-79-24-14-12-15-25-79)182-138(230)105(61-117(211)212)185-130(222)94(42-45-113(156)207)171-124(216)75(7)170-127(219)91(31-22-49-165-151(160)161)172-128(220)92(32-23-50-166-152(162)163)174-145(237)109(68-199)190-147(239)111(70-243)192-134(226)98(53-73(3)4)178-135(227)99(56-81-33-37-85(204)38-34-81)180-129(221)90(30-20-21-48-153)173-144(236)108(67-198)189-136(228)100(57-82-35-39-86(205)40-36-82)181-139(231)106(62-118(213)214)186-146(238)110(69-200)191-150(242)122(78(10)203)196-141(233)102(55-80-26-16-13-17-27-80)187-149(241)121(77(9)202)193-116(210)65-168-126(218)93(41-44-112(155)206)175-143(235)107(66-197)188-125(217)88(154)59-84-64-164-71-169-84/h12-19,24-29,33-40,63-64,71-78,88,90-111,119-122,167,197-205,243H,20-23,30-32,41-62,65-70,153-154H2,1-11H3,(H2,155,206)(H2,156,207)(H2,157,208)(H2,158,209)(H2,159,215)(H,164,169)(H,168,218)(H,170,219)(H,171,216)(H,172,220)(H,173,236)(H,174,237)(H,175,235)(H,176,225)(H,177,240)(H,178,227)(H,179,229)(H,180,221)(H,181,231)(H,182,230)(H,183,223)(H,184,224)(H,185,222)(H,186,238)(H,187,241)(H,188,217)(H,189,228)(H,190,239)(H,191,242)(H,192,226)(H,193,210)(H,194,232)(H,195,234)(H,196,233)(H,211,212)(H,213,214)(H4,160,161,165)(H4,162,163,166)/t75-,76+,77+,78+,88-,90-,91-,92-,93-,94-,95-,96-,97-,98-,99-,100-,101-,102-,103-,104-,105-,106-,107-,108-,109-,110-,111-,119-,120-,121-,122-/m0/s1
PDB
MMDB

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
KEGG
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 0.460n/an/an/an/a



China Pharmaceutical University

Curated by ChEMBL


Assay Description
Agonist activity at human GCGR expressed in HEK293 cells assessed as increase in cAMP accumulation after 20 mins by HTRF assay


Eur J Med Chem 138: 1158-1169 (2017)


Article DOI: 10.1016/j.ejmech.2017.07.046
BindingDB Entry DOI: 10.7270/Q2QC061V
More data for this
Ligand-Target Pair
Glucagon receptor


(Homo sapiens (Human))
BDBM50277057
PNG
(CHEMBL4174154)
Show SMILES CCCCCCN1C(=O)CC(SC[C@H](NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)Cc2cnc[nH]2)[C@@H](C)O)[C@@H](C)O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](Cc2ccccc2)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](Cc2c[nH]c3ccccc23)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(N)=O)C1=O |r|
Show InChI InChI=1S/C163H241N45O49S2/c1-13-14-15-26-56-208-125(222)70-119(161(208)257)259-77-118(157(253)185-99(37-28-55-177-163(173)174)138(234)183-98(36-27-54-176-162(171)172)137(233)181-82(8)134(230)182-101(47-50-121(167)218)140(236)196-112(67-126(223)224)148(244)193-108(60-86-29-18-16-19-30-86)151(247)205-129(81(6)7)158(254)188-102(48-51-122(168)219)141(237)194-110(64-90-71-178-96-34-23-22-33-94(90)96)147(243)190-104(58-79(2)3)143(239)187-103(52-57-258-12)142(238)195-111(66-123(169)220)153(249)206-130(83(9)212)133(170)229)203-150(246)114(69-128(227)228)197-144(240)105(59-80(4)5)189-145(241)106(62-88-38-42-92(215)43-39-88)191-139(235)97(35-24-25-53-164)184-155(251)116(75-210)201-146(242)107(63-89-40-44-93(216)45-41-89)192-149(245)113(68-127(225)226)198-156(252)117(76-211)202-160(256)132(85(11)214)207-152(248)109(61-87-31-20-17-21-32-87)199-159(255)131(84(10)213)204-124(221)73-179-136(232)100(46-49-120(166)217)186-154(250)115(74-209)200-135(231)95(165)65-91-72-175-78-180-91/h16-23,29-34,38-45,71-72,78-85,95,97-119,129-132,178,209-216H,13-15,24-28,35-37,46-70,73-77,164-165H2,1-12H3,(H2,166,217)(H2,167,218)(H2,168,219)(H2,169,220)(H2,170,229)(H,175,180)(H,179,232)(H,181,233)(H,182,230)(H,183,234)(H,184,251)(H,185,253)(H,186,250)(H,187,239)(H,188,254)(H,189,241)(H,190,243)(H,191,235)(H,192,245)(H,193,244)(H,194,237)(H,195,238)(H,196,236)(H,197,240)(H,198,252)(H,199,255)(H,200,231)(H,201,242)(H,202,256)(H,203,246)(H,204,221)(H,205,247)(H,206,249)(H,207,248)(H,223,224)(H,225,226)(H,227,228)(H4,171,172,176)(H4,173,174,177)/t82-,83+,84+,85+,95-,97-,98-,99-,100-,101-,102-,103-,104-,105-,106-,107-,108-,109-,110-,111-,112-,113-,114-,115-,116-,117-,118-,119?,129-,130-,131-,132-/m0/s1
PDB
MMDB

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 0.860n/an/an/an/a



China Pharmaceutical University

Curated by ChEMBL


Assay Description
Agonist activity at human GCGR expressed in HEK293 cells assessed as increase in cAMP accumulation after 20 mins by HTRF assay


Eur J Med Chem 138: 1158-1169 (2017)


Article DOI: 10.1016/j.ejmech.2017.07.046
BindingDB Entry DOI: 10.7270/Q2QC061V
More data for this
Ligand-Target Pair
Glucagon-like peptide 1 receptor


(Homo sapiens (Human))
BDBM50277058
PNG
(CHEMBL4165144)
Show SMILES CSCC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CSC1CC(=O)N(CCCCCCCCCCCC(O)=O)C1=O)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CO)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)Cc1cnc[nH]1)[C@@H](C)O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(N)=O |r|
Show InChI InChI=1S/C169H251N45O52S2/c1-84(2)62-108(148(247)192-107(56-61-267-10)147(246)200-115(70-128(175)227)158(257)212-136(87(7)219)139(176)238)195-152(251)114(68-94-75-184-100-37-26-25-36-98(94)100)199-146(245)106(52-55-127(174)226)193-164(263)135(86(5)6)211-156(255)112(64-90-32-20-18-21-33-90)198-153(252)116(71-132(232)233)201-145(244)105(51-54-126(173)225)191-163(262)123(82-268-124-74-130(229)214(167(124)266)60-29-17-15-13-11-12-14-16-24-41-131(230)231)209-144(243)103(40-31-59-183-169(179)180)187-142(241)102(39-30-58-182-168(177)178)189-161(260)121(80-217)207-155(254)118(73-134(236)237)202-149(248)109(63-85(3)4)194-150(249)110(66-92-42-46-96(222)47-43-92)196-143(242)101(38-27-28-57-170)188-160(259)120(79-216)206-151(250)111(67-93-44-48-97(223)49-45-93)197-154(253)117(72-133(234)235)203-162(261)122(81-218)208-166(265)138(89(9)221)213-157(256)113(65-91-34-22-19-23-35-91)204-165(264)137(88(8)220)210-129(228)77-185-141(240)104(50-53-125(172)224)190-159(258)119(78-215)205-140(239)99(171)69-95-76-181-83-186-95/h18-23,25-26,32-37,42-49,75-76,83-89,99,101-124,135-138,184,215-223H,11-17,24,27-31,38-41,50-74,77-82,170-171H2,1-10H3,(H2,172,224)(H2,173,225)(H2,174,226)(H2,175,227)(H2,176,238)(H,181,186)(H,185,240)(H,187,241)(H,188,259)(H,189,260)(H,190,258)(H,191,262)(H,192,247)(H,193,263)(H,194,249)(H,195,251)(H,196,242)(H,197,253)(H,198,252)(H,199,245)(H,200,246)(H,201,244)(H,202,248)(H,203,261)(H,204,264)(H,205,239)(H,206,250)(H,207,254)(H,208,265)(H,209,243)(H,210,228)(H,211,255)(H,212,257)(H,213,256)(H,230,231)(H,232,233)(H,234,235)(H,236,237)(H4,177,178,182)(H4,179,180,183)/t87-,88-,89-,99+,101+,102+,103+,104+,105+,106+,107+,108+,109+,110+,111+,112+,113+,114+,115+,116+,117+,118+,119+,120+,121+,122+,123+,124?,135+,136+,137+,138+/m1/s1
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 3n/an/an/an/a



China Pharmaceutical University

Curated by ChEMBL


Assay Description
Agonist activity at full length human GLP1R expressed in HEK293 cells assessed as increase in cAMP accumulation after 20 mins by HTRF assay


Eur J Med Chem 138: 1158-1169 (2017)


Article DOI: 10.1016/j.ejmech.2017.07.046
BindingDB Entry DOI: 10.7270/Q2QC061V
More data for this
Ligand-Target Pair
Glucagon-like peptide 1 receptor


(Homo sapiens (Human))
BDBM50277059
PNG
(CHEMBL4177064)
Show SMILES CCCCCCCCCCCCN1C(=O)CC(SC[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)Cc2cnc[nH]2)[C@@H](C)O)[C@@H](C)O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](Cc2ccccc2)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](Cc2c[nH]c3ccccc23)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(N)=O)C1=O |r|
Show InChI InChI=1S/C166H246N42O50S2/c1-13-14-15-16-17-18-19-20-21-32-59-208-129(223)73-123(165(208)258)260-81-122(161(254)184-102(41-33-58-177-166(174)175)141(234)181-86(8)138(231)182-104(51-54-125(170)219)143(236)195-115(70-130(224)225)151(244)192-111(63-90-34-24-22-25-35-90)154(247)205-133(85(6)7)162(255)187-105(52-55-126(171)220)144(237)193-113(67-94-74-178-100-39-29-28-38-98(94)100)150(243)189-107(61-83(2)3)146(239)186-106(56-60-259-12)145(238)194-114(69-127(172)221)156(249)206-134(87(9)213)137(173)230)203-160(253)120(79-211)201-153(246)117(72-132(228)229)196-147(240)108(62-84(4)5)188-148(241)109(65-92-42-46-96(216)47-43-92)190-142(235)101(40-30-31-57-167)183-158(251)119(78-210)200-149(242)110(66-93-44-48-97(217)49-45-93)191-152(245)116(71-131(226)227)197-159(252)121(80-212)202-164(257)136(89(11)215)207-155(248)112(64-91-36-26-23-27-37-91)198-163(256)135(88(10)214)204-128(222)76-179-140(233)103(50-53-124(169)218)185-157(250)118(77-209)199-139(232)99(168)68-95-75-176-82-180-95/h22-29,34-39,42-49,74-75,82-89,99,101-123,133-136,178,209-217H,13-21,30-33,40-41,50-73,76-81,167-168H2,1-12H3,(H2,169,218)(H2,170,219)(H2,171,220)(H2,172,221)(H2,173,230)(H,176,180)(H,179,233)(H,181,234)(H,182,231)(H,183,251)(H,184,254)(H,185,250)(H,186,239)(H,187,255)(H,188,241)(H,189,243)(H,190,235)(H,191,245)(H,192,244)(H,193,237)(H,194,238)(H,195,236)(H,196,240)(H,197,252)(H,198,256)(H,199,232)(H,200,242)(H,201,246)(H,202,257)(H,203,253)(H,204,222)(H,205,247)(H,206,249)(H,207,248)(H,224,225)(H,226,227)(H,228,229)(H4,174,175,177)/t86-,87+,88+,89+,99-,101-,102-,103-,104-,105-,106-,107-,108-,109-,110-,111-,112-,113-,114-,115-,116-,117-,118-,119-,120-,121-,122-,123?,133-,134-,135-,136-/m0/s1
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 2n/an/an/an/a



China Pharmaceutical University

Curated by ChEMBL


Assay Description
Agonist activity at full length human GLP1R expressed in HEK293 cells assessed as increase in cAMP accumulation after 20 mins by HTRF assay


Eur J Med Chem 138: 1158-1169 (2017)


Article DOI: 10.1016/j.ejmech.2017.07.046
BindingDB Entry DOI: 10.7270/Q2QC061V
More data for this
Ligand-Target Pair
Glucagon-like peptide 1 receptor


(Homo sapiens (Human))
BDBM50277055
PNG
(CHEMBL4169653)
Show SMILES CCCCCCCCCCCCN1C(=O)CC(SC[C@H](NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)Cc2cnc[nH]2)[C@@H](C)O)[C@@H](C)O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](Cc2ccccc2)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](Cc2c[nH]c3ccccc23)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(N)=O)C1=O |r|
Show InChI InChI=1S/C169H253N45O49S2/c1-13-14-15-16-17-18-19-20-21-32-62-214-131(228)76-125(167(214)263)265-83-124(163(259)191-105(43-34-61-183-169(179)180)144(240)189-104(42-33-60-182-168(177)178)143(239)187-88(8)140(236)188-107(53-56-127(173)224)146(242)202-118(73-132(229)230)154(250)199-114(66-92-35-24-22-25-36-92)157(253)211-135(87(6)7)164(260)194-108(54-57-128(174)225)147(243)200-116(70-96-77-184-102-40-29-28-39-100(96)102)153(249)196-110(64-85(2)3)149(245)193-109(58-63-264-12)148(244)201-117(72-129(175)226)159(255)212-136(89(9)218)139(176)235)209-156(252)120(75-134(233)234)203-150(246)111(65-86(4)5)195-151(247)112(68-94-44-48-98(221)49-45-94)197-145(241)103(41-30-31-59-170)190-161(257)122(81-216)207-152(248)113(69-95-46-50-99(222)51-47-95)198-155(251)119(74-133(231)232)204-162(258)123(82-217)208-166(262)138(91(11)220)213-158(254)115(67-93-37-26-23-27-38-93)205-165(261)137(90(10)219)210-130(227)79-185-142(238)106(52-55-126(172)223)192-160(256)121(80-215)206-141(237)101(171)71-97-78-181-84-186-97/h22-29,35-40,44-51,77-78,84-91,101,103-125,135-138,184,215-222H,13-21,30-34,41-43,52-76,79-83,170-171H2,1-12H3,(H2,172,223)(H2,173,224)(H2,174,225)(H2,175,226)(H2,176,235)(H,181,186)(H,185,238)(H,187,239)(H,188,236)(H,189,240)(H,190,257)(H,191,259)(H,192,256)(H,193,245)(H,194,260)(H,195,247)(H,196,249)(H,197,241)(H,198,251)(H,199,250)(H,200,243)(H,201,244)(H,202,242)(H,203,246)(H,204,258)(H,205,261)(H,206,237)(H,207,248)(H,208,262)(H,209,252)(H,210,227)(H,211,253)(H,212,255)(H,213,254)(H,229,230)(H,231,232)(H,233,234)(H4,177,178,182)(H4,179,180,183)/t88-,89+,90+,91+,101-,103-,104-,105-,106-,107-,108-,109-,110-,111-,112-,113-,114-,115-,116-,117-,118-,119-,120-,121-,122-,123-,124-,125?,135-,136-,137-,138-/m0/s1
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 4.5n/an/an/an/a



China Pharmaceutical University

Curated by ChEMBL


Assay Description
Agonist activity at full length human GLP1R expressed in HEK293 cells assessed as increase in cAMP accumulation after 20 mins by HTRF assay


Eur J Med Chem 138: 1158-1169 (2017)


Article DOI: 10.1016/j.ejmech.2017.07.046
BindingDB Entry DOI: 10.7270/Q2QC061V
More data for this
Ligand-Target Pair
Glucagon-like peptide 1 receptor


(Homo sapiens (Human))
BDBM50277060
PNG
(CHEMBL4167331)
Show SMILES CSCC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CS)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CO)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)Cc1cnc[nH]1)[C@@H](C)O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(N)=O |r|
Show InChI InChI=1S/C152H226N44O46S2/c1-72(2)52-97(133(225)176-96(47-51-244-11)132(224)184-104(60-115(158)209)142(234)195-120(76(8)201)123(159)215)179-137(229)103(58-83-63-167-89-29-19-18-28-87(83)89)183-130(222)95(43-46-114(157)208)177-148(240)119(74(5)6)194-140(232)101(54-79-24-14-12-15-25-79)182-147(239)111(70-243)192-131(223)94(42-45-113(156)207)171-124(216)75(7)170-127(219)91(31-22-49-165-151(160)161)172-128(220)92(32-23-50-166-152(162)163)174-145(237)109(68-199)190-139(231)106(62-118(213)214)185-134(226)98(53-73(3)4)178-135(227)99(56-81-33-37-85(204)38-34-81)180-129(221)90(30-20-21-48-153)173-144(236)108(67-198)189-136(228)100(57-82-35-39-86(205)40-36-82)181-138(230)105(61-117(211)212)186-146(238)110(69-200)191-150(242)122(78(10)203)196-141(233)102(55-80-26-16-13-17-27-80)187-149(241)121(77(9)202)193-116(210)65-168-126(218)93(41-44-112(155)206)175-143(235)107(66-197)188-125(217)88(154)59-84-64-164-71-169-84/h12-19,24-29,33-40,63-64,71-78,88,90-111,119-122,167,197-205,243H,20-23,30-32,41-62,65-70,153-154H2,1-11H3,(H2,155,206)(H2,156,207)(H2,157,208)(H2,158,209)(H2,159,215)(H,164,169)(H,168,218)(H,170,219)(H,171,216)(H,172,220)(H,173,236)(H,174,237)(H,175,235)(H,176,225)(H,177,240)(H,178,227)(H,179,229)(H,180,221)(H,181,230)(H,182,239)(H,183,222)(H,184,224)(H,185,226)(H,186,238)(H,187,241)(H,188,217)(H,189,228)(H,190,231)(H,191,242)(H,192,223)(H,193,210)(H,194,232)(H,195,234)(H,196,233)(H,211,212)(H,213,214)(H4,160,161,165)(H4,162,163,166)/t75-,76+,77+,78+,88-,90-,91-,92-,93-,94-,95-,96-,97-,98-,99-,100-,101-,102-,103-,104-,105-,106-,107-,108-,109-,110-,111-,119-,120-,121-,122-/m0/s1
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
KEGG
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 6.10n/an/an/an/a



China Pharmaceutical University

Curated by ChEMBL


Assay Description
Agonist activity at full length human GLP1R expressed in HEK293 cells assessed as increase in cAMP accumulation after 20 mins by HTRF assay


Eur J Med Chem 138: 1158-1169 (2017)


Article DOI: 10.1016/j.ejmech.2017.07.046
BindingDB Entry DOI: 10.7270/Q2QC061V
More data for this
Ligand-Target Pair
Glucagon-like peptide 1 receptor


(Homo sapiens (Human))
BDBM50277061
PNG
(CHEMBL4159256)
Show SMILES CSCC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CS)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)Cc1cnc[nH]1)[C@@H](C)O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(N)=O |r|
Show InChI InChI=1S/C153H226N44O47S2/c1-72(2)52-97(134(227)177-96(47-51-246-11)133(226)185-104(60-115(159)209)144(237)196-121(76(8)201)124(160)217)180-138(231)103(58-83-64-168-89-29-19-18-28-87(83)89)184-132(225)95(43-46-114(158)208)178-149(242)120(74(5)6)195-142(235)101(54-79-24-14-12-15-25-79)183-139(232)105(61-117(211)212)186-131(224)94(42-45-113(157)207)172-125(218)75(7)171-128(221)91(31-22-49-166-152(161)162)173-129(222)92(32-23-50-167-153(163)164)175-148(241)111(70-245)193-141(234)107(63-119(215)216)187-135(228)98(53-73(3)4)179-136(229)99(56-81-33-37-85(204)38-34-81)181-130(223)90(30-20-21-48-154)174-146(239)109(68-199)191-137(230)100(57-82-35-39-86(205)40-36-82)182-140(233)106(62-118(213)214)188-147(240)110(69-200)192-151(244)123(78(10)203)197-143(236)102(55-80-26-16-13-17-27-80)189-150(243)122(77(9)202)194-116(210)66-169-127(220)93(41-44-112(156)206)176-145(238)108(67-198)190-126(219)88(155)59-84-65-165-71-170-84/h12-19,24-29,33-40,64-65,71-78,88,90-111,120-123,168,198-205,245H,20-23,30-32,41-63,66-70,154-155H2,1-11H3,(H2,156,206)(H2,157,207)(H2,158,208)(H2,159,209)(H2,160,217)(H,165,170)(H,169,220)(H,171,221)(H,172,218)(H,173,222)(H,174,239)(H,175,241)(H,176,238)(H,177,227)(H,178,242)(H,179,229)(H,180,231)(H,181,223)(H,182,233)(H,183,232)(H,184,225)(H,185,226)(H,186,224)(H,187,228)(H,188,240)(H,189,243)(H,190,219)(H,191,230)(H,192,244)(H,193,234)(H,194,210)(H,195,235)(H,196,237)(H,197,236)(H,211,212)(H,213,214)(H,215,216)(H4,161,162,166)(H4,163,164,167)/t75-,76+,77+,78+,88-,90-,91-,92-,93-,94-,95-,96-,97-,98-,99-,100-,101-,102-,103-,104-,105-,106-,107-,108-,109-,110-,111-,120-,121-,122-,123-/m0/s1
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
KEGG
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 0.940n/an/an/an/a



China Pharmaceutical University

Curated by ChEMBL


Assay Description
Agonist activity at full length human GLP1R expressed in HEK293 cells assessed as increase in cAMP accumulation after 20 mins by HTRF assay


Eur J Med Chem 138: 1158-1169 (2017)


Article DOI: 10.1016/j.ejmech.2017.07.046
BindingDB Entry DOI: 10.7270/Q2QC061V
More data for this
Ligand-Target Pair
Glucagon-like peptide 1 receptor


(Homo sapiens (Human))
BDBM50277062
PNG
(CHEMBL4175452)
Show SMILES CSCC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CO)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)Cc1cnc[nH]1)[C@@H](C)O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(N)=O |r|
Show InChI InChI=1S/C153H226N44O48S/c1-72(2)52-97(134(228)177-96(47-51-246-11)133(227)185-104(60-115(159)210)144(238)196-121(76(8)202)124(160)218)180-138(232)103(58-83-64-168-89-29-19-18-28-87(83)89)184-132(226)95(43-46-114(158)209)178-149(243)120(74(5)6)195-142(236)101(54-79-24-14-12-15-25-79)183-139(233)105(61-117(212)213)186-131(225)94(42-45-113(157)208)172-125(219)75(7)171-128(222)91(31-22-49-166-152(161)162)173-129(223)92(32-23-50-167-153(163)164)175-147(241)110(69-200)192-141(235)107(63-119(216)217)187-135(229)98(53-73(3)4)179-136(230)99(56-81-33-37-85(205)38-34-81)181-130(224)90(30-20-21-48-154)174-146(240)109(68-199)191-137(231)100(57-82-35-39-86(206)40-36-82)182-140(234)106(62-118(214)215)188-148(242)111(70-201)193-151(245)123(78(10)204)197-143(237)102(55-80-26-16-13-17-27-80)189-150(244)122(77(9)203)194-116(211)66-169-127(221)93(41-44-112(156)207)176-145(239)108(67-198)190-126(220)88(155)59-84-65-165-71-170-84/h12-19,24-29,33-40,64-65,71-78,88,90-111,120-123,168,198-206H,20-23,30-32,41-63,66-70,154-155H2,1-11H3,(H2,156,207)(H2,157,208)(H2,158,209)(H2,159,210)(H2,160,218)(H,165,170)(H,169,221)(H,171,222)(H,172,219)(H,173,223)(H,174,240)(H,175,241)(H,176,239)(H,177,228)(H,178,243)(H,179,230)(H,180,232)(H,181,224)(H,182,234)(H,183,233)(H,184,226)(H,185,227)(H,186,225)(H,187,229)(H,188,242)(H,189,244)(H,190,220)(H,191,231)(H,192,235)(H,193,245)(H,194,211)(H,195,236)(H,196,238)(H,197,237)(H,212,213)(H,214,215)(H,216,217)(H4,161,162,166)(H4,163,164,167)/t75-,76+,77+,78+,88-,90-,91-,92-,93-,94-,95-,96-,97-,98-,99-,100-,101-,102-,103-,104-,105-,106-,107-,108-,109-,110-,111-,120-,121-,122-,123-/m0/s1
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Patents


Similars

Article
PubMed
n/an/an/an/a 3.20n/an/an/an/a



China Pharmaceutical University

Curated by ChEMBL


Assay Description
Agonist activity at full length human GLP1R expressed in HEK293 cells assessed as increase in cAMP accumulation after 20 mins by HTRF assay


Eur J Med Chem 138: 1158-1169 (2017)


Article DOI: 10.1016/j.ejmech.2017.07.046
BindingDB Entry DOI: 10.7270/Q2QC061V
More data for this
Ligand-Target Pair
Glucagon receptor


(Homo sapiens (Human))
BDBM50277063
PNG
(CHEMBL4163731)
Show SMILES CSCC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CSC1CC(=O)N(CCCCCCCCCCCC(O)=O)C1=O)NC(=O)[C@H](CO)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)Cc1cnc[nH]1)[C@@H](C)O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(N)=O |r|
Show InChI InChI=1S/C166H244N42O52S2/c1-82(2)60-106(146(241)186-105(55-59-261-11)145(240)194-113(68-126(172)221)156(251)206-134(86(8)213)137(173)232)189-150(245)112(66-93-73-178-99-37-27-26-36-97(93)99)193-144(239)104(51-54-125(171)220)187-162(257)133(84(5)6)205-154(249)110(62-89-32-21-19-22-33-89)192-151(246)114(69-130(226)227)195-143(238)103(50-53-124(170)219)182-138(233)85(7)181-141(236)101(39-31-57-177-166(174)175)184-161(256)121(80-262-122-72-128(223)208(165(122)260)58-30-18-16-14-12-13-15-17-25-40-129(224)225)203-160(255)119(78-211)201-153(248)116(71-132(230)231)196-147(242)107(61-83(3)4)188-148(243)108(64-91-41-45-95(216)46-42-91)190-142(237)100(38-28-29-56-167)183-158(253)118(77-210)200-149(244)109(65-92-43-47-96(217)48-44-92)191-152(247)115(70-131(228)229)197-159(254)120(79-212)202-164(259)136(88(10)215)207-155(250)111(63-90-34-23-20-24-35-90)198-163(258)135(87(9)214)204-127(222)75-179-140(235)102(49-52-123(169)218)185-157(252)117(76-209)199-139(234)98(168)67-94-74-176-81-180-94/h19-24,26-27,32-37,41-48,73-74,81-88,98,100-122,133-136,178,209-217H,12-18,25,28-31,38-40,49-72,75-80,167-168H2,1-11H3,(H2,169,218)(H2,170,219)(H2,171,220)(H2,172,221)(H2,173,232)(H,176,180)(H,179,235)(H,181,236)(H,182,233)(H,183,253)(H,184,256)(H,185,252)(H,186,241)(H,187,257)(H,188,243)(H,189,245)(H,190,237)(H,191,247)(H,192,246)(H,193,239)(H,194,240)(H,195,238)(H,196,242)(H,197,254)(H,198,258)(H,199,234)(H,200,244)(H,201,248)(H,202,259)(H,203,255)(H,204,222)(H,205,249)(H,206,251)(H,207,250)(H,224,225)(H,226,227)(H,228,229)(H,230,231)(H4,174,175,177)/t85-,86+,87+,88+,98-,100-,101-,102-,103-,104-,105-,106-,107-,108-,109-,110-,111-,112-,113-,114-,115-,116-,117-,118-,119-,120-,121-,122?,133-,134-,135-,136-/m0/s1
PDB
MMDB

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Patents

Article
PubMed
n/an/an/an/a 2.80n/an/an/an/a



China Pharmaceutical University

Curated by ChEMBL


Assay Description
Agonist activity at human GCGR expressed in HEK293 cells assessed as increase in cAMP accumulation after 20 mins by HTRF assay


Eur J Med Chem 138: 1158-1169 (2017)


Article DOI: 10.1016/j.ejmech.2017.07.046
BindingDB Entry DOI: 10.7270/Q2QC061V
More data for this
Ligand-Target Pair
Glucagon receptor


(Homo sapiens (Human))
BDBM50277068
PNG
(CHEMBL4167169)
Show SMILES CSCC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CS)NC(=O)[C@H](CO)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)Cc1cnc[nH]1)[C@@H](C)O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(N)=O |r|
Show InChI InChI=1S/C150H219N41O48S2/c1-70(2)49-94(131(221)170-93(45-48-241-11)130(220)178-101(57-113(156)204)141(231)190-119(74(8)196)122(157)212)173-135(225)100(55-81-61-162-87-28-19-18-27-85(81)87)177-129(219)92(41-44-112(155)203)171-147(237)118(72(5)6)189-139(229)98(51-77-23-14-12-15-24-77)176-136(226)102(58-115(206)207)179-128(218)91(40-43-111(154)202)166-123(213)73(7)165-126(216)89(30-22-47-161-150(158)159)168-146(236)109(68-240)187-145(235)107(66-194)185-138(228)104(60-117(210)211)180-132(222)95(50-71(3)4)172-133(223)96(53-79-31-35-83(199)36-32-79)174-127(217)88(29-20-21-46-151)167-143(233)106(65-193)184-134(224)97(54-80-33-37-84(200)38-34-80)175-137(227)103(59-116(208)209)181-144(234)108(67-195)186-149(239)121(76(10)198)191-140(230)99(52-78-25-16-13-17-26-78)182-148(238)120(75(9)197)188-114(205)63-163-125(215)90(39-42-110(153)201)169-142(232)105(64-192)183-124(214)86(152)56-82-62-160-69-164-82/h12-19,23-28,31-38,61-62,69-76,86,88-109,118-121,162,192-200,240H,20-22,29-30,39-60,63-68,151-152H2,1-11H3,(H2,153,201)(H2,154,202)(H2,155,203)(H2,156,204)(H2,157,212)(H,160,164)(H,163,215)(H,165,216)(H,166,213)(H,167,233)(H,168,236)(H,169,232)(H,170,221)(H,171,237)(H,172,223)(H,173,225)(H,174,217)(H,175,227)(H,176,226)(H,177,219)(H,178,220)(H,179,218)(H,180,222)(H,181,234)(H,182,238)(H,183,214)(H,184,224)(H,185,228)(H,186,239)(H,187,235)(H,188,205)(H,189,229)(H,190,231)(H,191,230)(H,206,207)(H,208,209)(H,210,211)(H4,158,159,161)/t73-,74+,75+,76+,86-,88-,89-,90-,91-,92-,93-,94-,95-,96-,97-,98-,99-,100-,101-,102-,103-,104-,105-,106-,107-,108-,109-,118-,119-,120-,121-/m0/s1
PDB
MMDB

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
KEGG
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 1.40n/an/an/an/a



China Pharmaceutical University

Curated by ChEMBL


Assay Description
Agonist activity at human GCGR expressed in HEK293 cells assessed as increase in cAMP accumulation after 20 mins by HTRF assay


Eur J Med Chem 138: 1158-1169 (2017)


Article DOI: 10.1016/j.ejmech.2017.07.046
BindingDB Entry DOI: 10.7270/Q2QC061V
More data for this
Ligand-Target Pair
Glucagon-like peptide 1 receptor


(Homo sapiens (Human))
BDBM50277069
PNG
(CHEMBL4161800)
Show SMILES CSCC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CS)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CO)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)Cc1cnc[nH]1)[C@@H](C)O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(N)=O |r|
Show InChI InChI=1S/C153H226N44O48S2/c1-72(2)51-96(133(227)176-95(46-50-247-10)132(226)184-103(59-115(159)210)143(237)196-121(75(7)202)124(160)218)179-137(231)102(57-82-63-168-88-28-18-17-27-86(82)88)183-131(225)94(42-45-114(158)209)177-149(243)120(74(5)6)195-141(235)100(53-78-23-13-11-14-24-78)182-138(232)104(60-117(212)213)185-130(224)93(41-44-113(157)208)175-148(242)111(70-246)193-129(223)91(31-22-49-167-153(163)164)171-127(221)90(30-21-48-166-152(161)162)173-146(240)109(68-200)191-140(234)106(62-119(216)217)186-134(228)97(52-73(3)4)178-135(229)98(55-80-32-36-84(205)37-33-80)180-128(222)89(29-19-20-47-154)172-145(239)108(67-199)190-136(230)99(56-81-34-38-85(206)39-35-81)181-139(233)105(61-118(214)215)187-147(241)110(69-201)192-151(245)123(77(9)204)197-142(236)101(54-79-25-15-12-16-26-79)188-150(244)122(76(8)203)194-116(211)65-169-126(220)92(40-43-112(156)207)174-144(238)107(66-198)189-125(219)87(155)58-83-64-165-71-170-83/h11-18,23-28,32-39,63-64,71-77,87,89-111,120-123,168,198-206,246H,19-22,29-31,40-62,65-70,154-155H2,1-10H3,(H2,156,207)(H2,157,208)(H2,158,209)(H2,159,210)(H2,160,218)(H,165,170)(H,169,220)(H,171,221)(H,172,239)(H,173,240)(H,174,238)(H,175,242)(H,176,227)(H,177,243)(H,178,229)(H,179,231)(H,180,222)(H,181,233)(H,182,232)(H,183,225)(H,184,226)(H,185,224)(H,186,228)(H,187,241)(H,188,244)(H,189,219)(H,190,230)(H,191,234)(H,192,245)(H,193,223)(H,194,211)(H,195,235)(H,196,237)(H,197,236)(H,212,213)(H,214,215)(H,216,217)(H4,161,162,166)(H4,163,164,167)/t75-,76-,77-,87+,89+,90+,91+,92+,93+,94+,95+,96+,97+,98+,99+,100+,101+,102+,103+,104+,105+,106+,107+,108+,109+,110+,111+,120+,121+,122+,123+/m1/s1
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
KEGG
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 1.70n/an/an/an/a



China Pharmaceutical University

Curated by ChEMBL


Assay Description
Agonist activity at full length human GLP1R expressed in HEK293 cells assessed as increase in cAMP accumulation after 20 mins by HTRF assay


Eur J Med Chem 138: 1158-1169 (2017)


Article DOI: 10.1016/j.ejmech.2017.07.046
BindingDB Entry DOI: 10.7270/Q2QC061V
More data for this
Ligand-Target Pair
Glucagon receptor


(Homo sapiens (Human))
BDBM50277070
PNG
(CHEMBL4170976)
Show SMILES CCCCCCCCCCCCCCCCN1C(=O)CC(SC[C@H](NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CO)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)Cc2cnc[nH]2)[C@@H](C)O)[C@@H](C)O)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](Cc2ccccc2)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](Cc2c[nH]c3ccccc23)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(N)=O)C1=O |r|
Show InChI InChI=1S/C173H261N45O50S2/c1-12-13-14-15-16-17-18-19-20-21-22-23-24-35-65-218-135(233)79-129(171(218)268)270-87-128(167(264)195-110(56-59-131(177)229)149(246)205-121(76-136(234)235)157(254)202-117(69-95-38-27-25-28-39-95)160(257)215-139(91(6)7)168(265)197-111(57-60-132(178)230)150(247)203-119(73-99-80-188-105-43-32-31-42-103(99)105)156(253)199-113(67-89(2)3)152(249)196-112(61-66-269-11)151(248)204-120(75-133(179)231)162(259)216-140(92(8)223)143(180)240)213-148(245)108(46-37-64-187-173(183)184)191-146(243)107(45-36-63-186-172(181)182)193-165(262)126(85-221)211-159(256)123(78-138(238)239)206-153(250)114(68-90(4)5)198-154(251)115(71-97-47-51-101(226)52-48-97)200-147(244)106(44-33-34-62-174)192-164(261)125(84-220)210-155(252)116(72-98-49-53-102(227)54-50-98)201-158(255)122(77-137(236)237)207-166(263)127(86-222)212-170(267)142(94(10)225)217-161(258)118(70-96-40-29-26-30-41-96)208-169(266)141(93(9)224)214-134(232)82-189-145(242)109(55-58-130(176)228)194-163(260)124(83-219)209-144(241)104(175)74-100-81-185-88-190-100/h25-32,38-43,47-54,80-81,88-94,104,106-129,139-142,188,219-227H,12-24,33-37,44-46,55-79,82-87,174-175H2,1-11H3,(H2,176,228)(H2,177,229)(H2,178,230)(H2,179,231)(H2,180,240)(H,185,190)(H,189,242)(H,191,243)(H,192,261)(H,193,262)(H,194,260)(H,195,264)(H,196,249)(H,197,265)(H,198,251)(H,199,253)(H,200,244)(H,201,255)(H,202,254)(H,203,247)(H,204,248)(H,205,246)(H,206,250)(H,207,263)(H,208,266)(H,209,241)(H,210,252)(H,211,256)(H,212,267)(H,213,245)(H,214,232)(H,215,257)(H,216,259)(H,217,258)(H,234,235)(H,236,237)(H,238,239)(H4,181,182,186)(H4,183,184,187)/t92-,93-,94-,104+,106+,107+,108+,109+,110+,111+,112+,113+,114+,115+,116+,117+,118+,119+,120+,121+,122+,123+,124+,125+,126+,127+,128+,129?,139+,140+,141+,142+/m1/s1
PDB
MMDB

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 19n/an/an/an/a



China Pharmaceutical University

Curated by ChEMBL


Assay Description
Agonist activity at human GCGR expressed in HEK293 cells assessed as increase in cAMP accumulation after 20 mins by HTRF assay


Eur J Med Chem 138: 1158-1169 (2017)


Article DOI: 10.1016/j.ejmech.2017.07.046
BindingDB Entry DOI: 10.7270/Q2QC061V
More data for this
Ligand-Target Pair
Glucagon receptor


(Homo sapiens (Human))
BDBM50277071
PNG
(CHEMBL4160365)
Show SMILES CCCCCCCCCCCCN1C(=O)CC(SC[C@H](NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CO)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)Cc2cnc[nH]2)[C@@H](C)O)[C@@H](C)O)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](Cc2ccccc2)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](Cc2c[nH]c3ccccc23)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(N)=O)C1=O |r|
Show InChI InChI=1S/C169H253N45O50S2/c1-12-13-14-15-16-17-18-19-20-31-61-214-131(229)75-125(167(214)264)266-83-124(163(260)191-106(52-55-127(173)225)145(242)201-117(72-132(230)231)153(250)198-113(65-91-34-23-21-24-35-91)156(253)211-135(87(6)7)164(261)193-107(53-56-128(174)226)146(243)199-115(69-95-76-184-101-39-28-27-38-99(95)101)152(249)195-109(63-85(2)3)148(245)192-108(57-62-265-11)147(244)200-116(71-129(175)227)158(255)212-136(88(8)219)139(176)236)209-144(241)104(42-33-60-183-169(179)180)187-142(239)103(41-32-59-182-168(177)178)189-161(258)122(81-217)207-155(252)119(74-134(234)235)202-149(246)110(64-86(4)5)194-150(247)111(67-93-43-47-97(222)48-44-93)196-143(240)102(40-29-30-58-170)188-160(257)121(80-216)206-151(248)112(68-94-45-49-98(223)50-46-94)197-154(251)118(73-133(232)233)203-162(259)123(82-218)208-166(263)138(90(10)221)213-157(254)114(66-92-36-25-22-26-37-92)204-165(262)137(89(9)220)210-130(228)78-185-141(238)105(51-54-126(172)224)190-159(256)120(79-215)205-140(237)100(171)70-96-77-181-84-186-96/h21-28,34-39,43-50,76-77,84-90,100,102-125,135-138,184,215-223H,12-20,29-33,40-42,51-75,78-83,170-171H2,1-11H3,(H2,172,224)(H2,173,225)(H2,174,226)(H2,175,227)(H2,176,236)(H,181,186)(H,185,238)(H,187,239)(H,188,257)(H,189,258)(H,190,256)(H,191,260)(H,192,245)(H,193,261)(H,194,247)(H,195,249)(H,196,240)(H,197,251)(H,198,250)(H,199,243)(H,200,244)(H,201,242)(H,202,246)(H,203,259)(H,204,262)(H,205,237)(H,206,248)(H,207,252)(H,208,263)(H,209,241)(H,210,228)(H,211,253)(H,212,255)(H,213,254)(H,230,231)(H,232,233)(H,234,235)(H4,177,178,182)(H4,179,180,183)/t88-,89-,90-,100+,102+,103+,104+,105+,106+,107+,108+,109+,110+,111+,112+,113+,114+,115+,116+,117+,118+,119+,120+,121+,122+,123+,124+,125?,135+,136+,137+,138+/m1/s1
PDB
MMDB

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Patents


Similars

Article
PubMed
n/an/an/an/a 4.80n/an/an/an/a



China Pharmaceutical University

Curated by ChEMBL


Assay Description
Agonist activity at human GCGR expressed in HEK293 cells assessed as increase in cAMP accumulation after 20 mins by HTRF assay


Eur J Med Chem 138: 1158-1169 (2017)


Article DOI: 10.1016/j.ejmech.2017.07.046
BindingDB Entry DOI: 10.7270/Q2QC061V
More data for this
Ligand-Target Pair
Glucagon receptor


(Homo sapiens (Human))
BDBM50277072
PNG
(CHEMBL4174404)
Show SMILES CCCCCCN1C(=O)CC(SC[C@H](NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CO)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)Cc2cnc[nH]2)[C@@H](C)O)[C@@H](C)O)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](Cc2ccccc2)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](Cc2c[nH]c3ccccc23)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(N)=O)C1=O |r|
Show InChI InChI=1S/C163H241N45O50S2/c1-12-13-14-25-55-208-125(223)69-119(161(208)258)260-77-118(157(254)185-100(46-49-121(167)219)139(236)195-111(66-126(224)225)147(244)192-107(59-85-28-17-15-18-29-85)150(247)205-129(81(6)7)158(255)187-101(47-50-122(168)220)140(237)193-109(63-89-70-178-95-33-22-21-32-93(89)95)146(243)189-103(57-79(2)3)142(239)186-102(51-56-259-11)141(238)194-110(65-123(169)221)152(249)206-130(82(8)213)133(170)230)203-138(235)98(36-27-54-177-163(173)174)181-136(233)97(35-26-53-176-162(171)172)183-155(252)116(75-211)201-149(246)113(68-128(228)229)196-143(240)104(58-80(4)5)188-144(241)105(61-87-37-41-91(216)42-38-87)190-137(234)96(34-23-24-52-164)182-154(251)115(74-210)200-145(242)106(62-88-39-43-92(217)44-40-88)191-148(245)112(67-127(226)227)197-156(253)117(76-212)202-160(257)132(84(10)215)207-151(248)108(60-86-30-19-16-20-31-86)198-159(256)131(83(9)214)204-124(222)72-179-135(232)99(45-48-120(166)218)184-153(250)114(73-209)199-134(231)94(165)64-90-71-175-78-180-90/h15-22,28-33,37-44,70-71,78-84,94,96-119,129-132,178,209-217H,12-14,23-27,34-36,45-69,72-77,164-165H2,1-11H3,(H2,166,218)(H2,167,219)(H2,168,220)(H2,169,221)(H2,170,230)(H,175,180)(H,179,232)(H,181,233)(H,182,251)(H,183,252)(H,184,250)(H,185,254)(H,186,239)(H,187,255)(H,188,241)(H,189,243)(H,190,234)(H,191,245)(H,192,244)(H,193,237)(H,194,238)(H,195,236)(H,196,240)(H,197,253)(H,198,256)(H,199,231)(H,200,242)(H,201,246)(H,202,257)(H,203,235)(H,204,222)(H,205,247)(H,206,249)(H,207,248)(H,224,225)(H,226,227)(H,228,229)(H4,171,172,176)(H4,173,174,177)/t82-,83-,84-,94+,96+,97+,98+,99+,100+,101+,102+,103+,104+,105+,106+,107+,108+,109+,110+,111+,112+,113+,114+,115+,116+,117+,118+,119?,129+,130+,131+,132+/m1/s1
PDB
MMDB

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 2.80n/an/an/an/a



China Pharmaceutical University

Curated by ChEMBL


Assay Description
Agonist activity at human GCGR expressed in HEK293 cells assessed as increase in cAMP accumulation after 20 mins by HTRF assay


Eur J Med Chem 138: 1158-1169 (2017)


Article DOI: 10.1016/j.ejmech.2017.07.046
BindingDB Entry DOI: 10.7270/Q2QC061V
More data for this
Ligand-Target Pair
Glucagon receptor


(Homo sapiens (Human))
BDBM50277059
PNG
(CHEMBL4177064)
Show SMILES CCCCCCCCCCCCN1C(=O)CC(SC[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)Cc2cnc[nH]2)[C@@H](C)O)[C@@H](C)O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](Cc2ccccc2)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](Cc2c[nH]c3ccccc23)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(N)=O)C1=O |r|
Show InChI InChI=1S/C166H246N42O50S2/c1-13-14-15-16-17-18-19-20-21-32-59-208-129(223)73-123(165(208)258)260-81-122(161(254)184-102(41-33-58-177-166(174)175)141(234)181-86(8)138(231)182-104(51-54-125(170)219)143(236)195-115(70-130(224)225)151(244)192-111(63-90-34-24-22-25-35-90)154(247)205-133(85(6)7)162(255)187-105(52-55-126(171)220)144(237)193-113(67-94-74-178-100-39-29-28-38-98(94)100)150(243)189-107(61-83(2)3)146(239)186-106(56-60-259-12)145(238)194-114(69-127(172)221)156(249)206-134(87(9)213)137(173)230)203-160(253)120(79-211)201-153(246)117(72-132(228)229)196-147(240)108(62-84(4)5)188-148(241)109(65-92-42-46-96(216)47-43-92)190-142(235)101(40-30-31-57-167)183-158(251)119(78-210)200-149(242)110(66-93-44-48-97(217)49-45-93)191-152(245)116(71-131(226)227)197-159(252)121(80-212)202-164(257)136(89(11)215)207-155(248)112(64-91-36-26-23-27-37-91)198-163(256)135(88(10)214)204-128(222)76-179-140(233)103(50-53-124(169)218)185-157(250)118(77-209)199-139(232)99(168)68-95-75-176-82-180-95/h22-29,34-39,42-49,74-75,82-89,99,101-123,133-136,178,209-217H,13-21,30-33,40-41,50-73,76-81,167-168H2,1-12H3,(H2,169,218)(H2,170,219)(H2,171,220)(H2,172,221)(H2,173,230)(H,176,180)(H,179,233)(H,181,234)(H,182,231)(H,183,251)(H,184,254)(H,185,250)(H,186,239)(H,187,255)(H,188,241)(H,189,243)(H,190,235)(H,191,245)(H,192,244)(H,193,237)(H,194,238)(H,195,236)(H,196,240)(H,197,252)(H,198,256)(H,199,232)(H,200,242)(H,201,246)(H,202,257)(H,203,253)(H,204,222)(H,205,247)(H,206,249)(H,207,248)(H,224,225)(H,226,227)(H,228,229)(H4,174,175,177)/t86-,87+,88+,89+,99-,101-,102-,103-,104-,105-,106-,107-,108-,109-,110-,111-,112-,113-,114-,115-,116-,117-,118-,119-,120-,121-,122-,123?,133-,134-,135-,136-/m0/s1
PDB
MMDB

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 3n/an/an/an/a



China Pharmaceutical University

Curated by ChEMBL


Assay Description
Agonist activity at human GCGR expressed in HEK293 cells assessed as increase in cAMP accumulation after 20 mins by HTRF assay


Eur J Med Chem 138: 1158-1169 (2017)


Article DOI: 10.1016/j.ejmech.2017.07.046
BindingDB Entry DOI: 10.7270/Q2QC061V
More data for this
Ligand-Target Pair
Glucagon receptor


(Homo sapiens (Human))
BDBM50277073
PNG
(CHEMBL4173061)
Show SMILES CSCC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CSC1CC(=O)N(CCCCCCCCCCCC(O)=O)C1=O)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)Cc1cnc[nH]1)[C@@H](C)O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(N)=O |r|
Show InChI InChI=1S/C169H251N45O51S2/c1-84(2)63-109(149(247)193-108(57-62-266-11)148(246)201-116(71-128(175)226)159(257)212-136(88(8)218)139(176)237)196-153(251)115(69-95-76-184-101-38-27-26-37-99(95)101)200-147(245)107(53-56-127(174)225)194-164(262)135(86(5)6)211-157(255)113(65-91-33-21-19-22-34-91)199-154(252)117(72-132(231)232)202-146(244)106(52-55-126(173)224)188-140(238)87(7)187-143(241)103(40-31-59-182-168(177)178)189-144(242)104(41-32-60-183-169(179)180)191-163(261)123(82-267-124-75-130(228)214(167(124)265)61-30-18-16-14-12-13-15-17-25-42-131(229)230)209-156(254)119(74-134(235)236)203-150(248)110(64-85(3)4)195-151(249)111(67-93-43-47-97(221)48-44-93)197-145(243)102(39-28-29-58-170)190-161(259)121(80-216)207-152(250)112(68-94-45-49-98(222)50-46-94)198-155(253)118(73-133(233)234)204-162(260)122(81-217)208-166(264)138(90(10)220)213-158(256)114(66-92-35-23-20-24-36-92)205-165(263)137(89(9)219)210-129(227)78-185-142(240)105(51-54-125(172)223)192-160(258)120(79-215)206-141(239)100(171)70-96-77-181-83-186-96/h19-24,26-27,33-38,43-50,76-77,83-90,100,102-124,135-138,184,215-222H,12-18,25,28-32,39-42,51-75,78-82,170-171H2,1-11H3,(H2,172,223)(H2,173,224)(H2,174,225)(H2,175,226)(H2,176,237)(H,181,186)(H,185,240)(H,187,241)(H,188,238)(H,189,242)(H,190,259)(H,191,261)(H,192,258)(H,193,247)(H,194,262)(H,195,249)(H,196,251)(H,197,243)(H,198,253)(H,199,252)(H,200,245)(H,201,246)(H,202,244)(H,203,248)(H,204,260)(H,205,263)(H,206,239)(H,207,250)(H,208,264)(H,209,254)(H,210,227)(H,211,255)(H,212,257)(H,213,256)(H,229,230)(H,231,232)(H,233,234)(H,235,236)(H4,177,178,182)(H4,179,180,183)/t87-,88+,89+,90+,100-,102-,103-,104-,105-,106-,107-,108-,109-,110-,111-,112-,113-,114-,115-,116-,117-,118-,119-,120-,121-,122-,123-,124?,135-,136-,137-,138-/m0/s1
PDB
MMDB

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 1.60n/an/an/an/a



China Pharmaceutical University

Curated by ChEMBL


Assay Description
Agonist activity at human GCGR expressed in HEK293 cells assessed as increase in cAMP accumulation after 20 mins by HTRF assay


Eur J Med Chem 138: 1158-1169 (2017)


Article DOI: 10.1016/j.ejmech.2017.07.046
BindingDB Entry DOI: 10.7270/Q2QC061V
More data for this
Ligand-Target Pair
Glucagon receptor


(Homo sapiens (Human))
BDBM50277074
PNG
(CHEMBL4166241)
Show SMILES CSCC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CS)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CO)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)Cc1cnc[nH]1)[C@@H](C)O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(N)=O |r|
Show InChI InChI=1S/C151H223N43O47S2/c1-71(2)50-95(131(223)174-94(45-49-243-11)130(222)181-102(58-113(156)206)141(233)193-119(75(8)199)122(157)214)176-135(227)101(56-82-62-165-88-29-19-18-28-86(82)88)180-146(238)110(69-242)190-147(239)118(73(5)6)192-139(231)99(52-78-24-14-12-15-25-78)179-136(228)103(59-115(208)209)182-129(221)93(42-44-112(155)205)169-123(215)74(7)168-126(218)90(31-22-47-163-150(158)159)170-127(219)91(32-23-48-164-151(160)161)172-144(236)108(67-197)188-138(230)105(61-117(212)213)183-132(224)96(51-72(3)4)175-133(225)97(54-80-33-37-84(202)38-34-80)177-128(220)89(30-20-21-46-152)171-143(235)107(66-196)187-134(226)98(55-81-35-39-85(203)40-36-81)178-137(229)104(60-116(210)211)184-145(237)109(68-198)189-149(241)121(77(10)201)194-140(232)100(53-79-26-16-13-17-27-79)185-148(240)120(76(9)200)191-114(207)64-166-125(217)92(41-43-111(154)204)173-142(234)106(65-195)186-124(216)87(153)57-83-63-162-70-167-83/h12-19,24-29,33-40,62-63,70-77,87,89-110,118-121,165,195-203,242H,20-23,30-32,41-61,64-69,152-153H2,1-11H3,(H2,154,204)(H2,155,205)(H2,156,206)(H2,157,214)(H,162,167)(H,166,217)(H,168,218)(H,169,215)(H,170,219)(H,171,235)(H,172,236)(H,173,234)(H,174,223)(H,175,225)(H,176,227)(H,177,220)(H,178,229)(H,179,228)(H,180,238)(H,181,222)(H,182,221)(H,183,224)(H,184,237)(H,185,240)(H,186,216)(H,187,226)(H,188,230)(H,189,241)(H,190,239)(H,191,207)(H,192,231)(H,193,233)(H,194,232)(H,208,209)(H,210,211)(H,212,213)(H4,158,159,163)(H4,160,161,164)/t74-,75+,76+,77+,87-,89-,90-,91-,92-,93-,94-,95-,96-,97-,98-,99-,100-,101-,102-,103-,104-,105-,106-,107-,108-,109-,110-,118-,119-,120-,121-/m0/s1
PDB
MMDB

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
KEGG
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 0.900n/an/an/an/a



China Pharmaceutical University

Curated by ChEMBL


Assay Description
Agonist activity at human GCGR expressed in HEK293 cells assessed as increase in cAMP accumulation after 20 mins by HTRF assay


Eur J Med Chem 138: 1158-1169 (2017)


Article DOI: 10.1016/j.ejmech.2017.07.046
BindingDB Entry DOI: 10.7270/Q2QC061V
More data for this
Ligand-Target Pair
Glucagon receptor


(Homo sapiens (Human))
BDBM50277078
PNG
(CHEMBL4170727)
Show SMILES CSCC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CS)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CO)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)Cc1cnc[nH]1)[C@@H](C)O)[C@@H](C)O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(N)=O |r|
Show InChI InChI=1S/C151H222N44O48S2/c1-71(2)50-95(132(226)176-94(45-49-245-9)131(225)183-102(58-114(157)208)142(236)194-119(74(6)200)122(158)216)178-137(231)101(56-81-62-166-87-27-17-16-26-85(81)87)182-130(224)93(41-44-113(156)207)175-147(241)110(69-244)192-136(230)97(52-77-22-12-10-13-23-77)180-138(232)103(59-116(210)211)184-129(223)92(40-43-112(155)206)170-123(217)73(5)169-126(220)89(29-20-47-164-150(159)160)171-127(221)90(30-21-48-165-151(161)162)173-145(239)108(67-198)190-140(234)105(61-118(214)215)185-133(227)96(51-72(3)4)177-134(228)98(54-79-31-35-83(203)36-32-79)179-128(222)88(28-18-19-46-152)172-144(238)107(66-197)189-135(229)99(55-80-33-37-84(204)38-34-80)181-139(233)104(60-117(212)213)186-146(240)109(68-199)191-149(243)121(76(8)202)195-141(235)100(53-78-24-14-11-15-25-78)187-148(242)120(75(7)201)193-115(209)64-167-125(219)91(39-42-111(154)205)174-143(237)106(65-196)188-124(218)86(153)57-82-63-163-70-168-82/h10-17,22-27,31-38,62-63,70-76,86,88-110,119-121,166,196-204,244H,18-21,28-30,39-61,64-69,152-153H2,1-9H3,(H2,154,205)(H2,155,206)(H2,156,207)(H2,157,208)(H2,158,216)(H,163,168)(H,167,219)(H,169,220)(H,170,217)(H,171,221)(H,172,238)(H,173,239)(H,174,237)(H,175,241)(H,176,226)(H,177,228)(H,178,231)(H,179,222)(H,180,232)(H,181,233)(H,182,224)(H,183,225)(H,184,223)(H,185,227)(H,186,240)(H,187,242)(H,188,218)(H,189,229)(H,190,234)(H,191,243)(H,192,230)(H,193,209)(H,194,236)(H,195,235)(H,210,211)(H,212,213)(H,214,215)(H4,159,160,164)(H4,161,162,165)/t73-,74+,75+,76+,86-,88-,89-,90-,91-,92-,93-,94-,95-,96-,97-,98-,99-,100-,101-,102-,103-,104-,105-,106-,107-,108-,109-,110-,119-,120-,121-/m0/s1
PDB
MMDB

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
KEGG
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 0.75n/an/an/an/a



China Pharmaceutical University

Curated by ChEMBL


Assay Description
Agonist activity at human GCGR expressed in HEK293 cells assessed as increase in cAMP accumulation after 20 mins by HTRF assay


Eur J Med Chem 138: 1158-1169 (2017)


Article DOI: 10.1016/j.ejmech.2017.07.046
BindingDB Entry DOI: 10.7270/Q2QC061V
More data for this
Ligand-Target Pair
Glucagon receptor


(Homo sapiens (Human))
BDBM50277079
PNG
(CHEMBL4162789)
Show SMILES CSCC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](CS)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CO)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)Cc1cnc[nH]1)[C@@H](C)O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(N)=O |r|
Show InChI InChI=1S/C147H222N44O48S2/c1-67(2)47-91(128(222)171-90(42-46-241-11)127(221)178-97(54-109(153)204)137(231)190-115(71(8)196)118(154)212)174-132(226)96(52-77-58-162-83-24-16-15-23-81(77)83)177-126(220)89(38-41-108(152)203)172-143(237)114(69(5)6)189-142(236)105(65-240)187-135(229)100(57-113(210)211)179-125(219)88(37-40-107(151)202)166-119(213)70(7)165-122(216)85(26-19-44-160-146(155)156)167-123(217)86(27-20-45-161-147(157)158)169-140(234)103(63-194)185-134(228)99(56-112(208)209)180-129(223)92(48-68(3)4)173-130(224)93(50-75-28-32-79(199)33-29-75)175-124(218)84(25-17-18-43-148)168-139(233)102(62-193)184-131(225)94(51-76-30-34-80(200)35-31-76)176-133(227)98(55-111(206)207)181-141(235)104(64-195)186-145(239)117(73(10)198)191-136(230)95(49-74-21-13-12-14-22-74)182-144(238)116(72(9)197)188-110(205)60-163-121(215)87(36-39-106(150)201)170-138(232)101(61-192)183-120(214)82(149)53-78-59-159-66-164-78/h12-16,21-24,28-35,58-59,66-73,82,84-105,114-117,162,192-200,240H,17-20,25-27,36-57,60-65,148-149H2,1-11H3,(H2,150,201)(H2,151,202)(H2,152,203)(H2,153,204)(H2,154,212)(H,159,164)(H,163,215)(H,165,216)(H,166,213)(H,167,217)(H,168,233)(H,169,234)(H,170,232)(H,171,222)(H,172,237)(H,173,224)(H,174,226)(H,175,218)(H,176,227)(H,177,220)(H,178,221)(H,179,219)(H,180,223)(H,181,235)(H,182,238)(H,183,214)(H,184,225)(H,185,228)(H,186,239)(H,187,229)(H,188,205)(H,189,236)(H,190,231)(H,191,230)(H,206,207)(H,208,209)(H,210,211)(H4,155,156,160)(H4,157,158,161)/t70-,71+,72+,73+,82-,84-,85-,86-,87-,88-,89-,90-,91-,92-,93-,94-,95-,96-,97-,98-,99-,100-,101-,102-,103-,104-,105-,114-,115-,116-,117-/m0/s1
PDB
MMDB

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
KEGG
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 123n/an/an/an/a



China Pharmaceutical University

Curated by ChEMBL


Assay Description
Agonist activity at human GCGR expressed in HEK293 cells assessed as increase in cAMP accumulation after 20 mins by HTRF assay


Eur J Med Chem 138: 1158-1169 (2017)


Article DOI: 10.1016/j.ejmech.2017.07.046
BindingDB Entry DOI: 10.7270/Q2QC061V
More data for this
Ligand-Target Pair
Glucagon receptor


(Homo sapiens (Human))
BDBM50277069
PNG
(CHEMBL4161800)
Show SMILES CSCC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CS)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CO)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)Cc1cnc[nH]1)[C@@H](C)O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(N)=O |r|
Show InChI InChI=1S/C153H226N44O48S2/c1-72(2)51-96(133(227)176-95(46-50-247-10)132(226)184-103(59-115(159)210)143(237)196-121(75(7)202)124(160)218)179-137(231)102(57-82-63-168-88-28-18-17-27-86(82)88)183-131(225)94(42-45-114(158)209)177-149(243)120(74(5)6)195-141(235)100(53-78-23-13-11-14-24-78)182-138(232)104(60-117(212)213)185-130(224)93(41-44-113(157)208)175-148(242)111(70-246)193-129(223)91(31-22-49-167-153(163)164)171-127(221)90(30-21-48-166-152(161)162)173-146(240)109(68-200)191-140(234)106(62-119(216)217)186-134(228)97(52-73(3)4)178-135(229)98(55-80-32-36-84(205)37-33-80)180-128(222)89(29-19-20-47-154)172-145(239)108(67-199)190-136(230)99(56-81-34-38-85(206)39-35-81)181-139(233)105(61-118(214)215)187-147(241)110(69-201)192-151(245)123(77(9)204)197-142(236)101(54-79-25-15-12-16-26-79)188-150(244)122(76(8)203)194-116(211)65-169-126(220)92(40-43-112(156)207)174-144(238)107(66-198)189-125(219)87(155)58-83-64-165-71-170-83/h11-18,23-28,32-39,63-64,71-77,87,89-111,120-123,168,198-206,246H,19-22,29-31,40-62,65-70,154-155H2,1-10H3,(H2,156,207)(H2,157,208)(H2,158,209)(H2,159,210)(H2,160,218)(H,165,170)(H,169,220)(H,171,221)(H,172,239)(H,173,240)(H,174,238)(H,175,242)(H,176,227)(H,177,243)(H,178,229)(H,179,231)(H,180,222)(H,181,233)(H,182,232)(H,183,225)(H,184,226)(H,185,224)(H,186,228)(H,187,241)(H,188,244)(H,189,219)(H,190,230)(H,191,234)(H,192,245)(H,193,223)(H,194,211)(H,195,235)(H,196,237)(H,197,236)(H,212,213)(H,214,215)(H,216,217)(H4,161,162,166)(H4,163,164,167)/t75-,76-,77-,87+,89+,90+,91+,92+,93+,94+,95+,96+,97+,98+,99+,100+,101+,102+,103+,104+,105+,106+,107+,108+,109+,110+,111+,120+,121+,122+,123+/m1/s1
PDB
MMDB

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
KEGG
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 7n/an/an/an/a



China Pharmaceutical University

Curated by ChEMBL


Assay Description
Agonist activity at human GCGR expressed in HEK293 cells assessed as increase in cAMP accumulation after 20 mins by HTRF assay


Eur J Med Chem 138: 1158-1169 (2017)


Article DOI: 10.1016/j.ejmech.2017.07.046
BindingDB Entry DOI: 10.7270/Q2QC061V
More data for this
Ligand-Target Pair
Glucagon receptor


(Homo sapiens (Human))
BDBM50277080
PNG
(CHEMBL4172444)
Show SMILES CSCC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](CS)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CO)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)Cc1cnc[nH]1)[C@@H](C)O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(N)=O |r|
Show InChI InChI=1S/C150H219N41O48S2/c1-70(2)49-94(131(221)170-93(45-48-241-11)130(220)178-101(57-113(156)204)141(231)190-119(74(8)196)122(157)212)173-135(225)100(55-81-61-162-87-28-19-18-27-85(81)87)177-129(219)92(41-44-112(155)203)171-147(237)118(72(5)6)189-139(229)98(51-77-23-14-12-15-24-77)176-136(226)102(58-115(206)207)179-128(218)91(40-43-111(154)202)166-123(213)73(7)165-146(236)109(68-240)187-127(217)89(30-22-47-161-150(158)159)168-144(234)107(66-194)185-138(228)104(60-117(210)211)180-132(222)95(50-71(3)4)172-133(223)96(53-79-31-35-83(199)36-32-79)174-126(216)88(29-20-21-46-151)167-143(233)106(65-193)184-134(224)97(54-80-33-37-84(200)38-34-80)175-137(227)103(59-116(208)209)181-145(235)108(67-195)186-149(239)121(76(10)198)191-140(230)99(52-78-25-16-13-17-26-78)182-148(238)120(75(9)197)188-114(205)63-163-125(215)90(39-42-110(153)201)169-142(232)105(64-192)183-124(214)86(152)56-82-62-160-69-164-82/h12-19,23-28,31-38,61-62,69-76,86,88-109,118-121,162,192-200,240H,20-22,29-30,39-60,63-68,151-152H2,1-11H3,(H2,153,201)(H2,154,202)(H2,155,203)(H2,156,204)(H2,157,212)(H,160,164)(H,163,215)(H,165,236)(H,166,213)(H,167,233)(H,168,234)(H,169,232)(H,170,221)(H,171,237)(H,172,223)(H,173,225)(H,174,216)(H,175,227)(H,176,226)(H,177,219)(H,178,220)(H,179,218)(H,180,222)(H,181,235)(H,182,238)(H,183,214)(H,184,224)(H,185,228)(H,186,239)(H,187,217)(H,188,205)(H,189,229)(H,190,231)(H,191,230)(H,206,207)(H,208,209)(H,210,211)(H4,158,159,161)/t73-,74+,75+,76+,86-,88-,89-,90-,91-,92-,93-,94-,95-,96-,97-,98-,99-,100-,101-,102-,103-,104-,105-,106-,107-,108-,109-,118-,119-,120-,121-/m0/s1
PDB
MMDB

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
KEGG
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 3.40n/an/an/an/a



China Pharmaceutical University

Curated by ChEMBL


Assay Description
Agonist activity at human GCGR expressed in HEK293 cells assessed as increase in cAMP accumulation after 20 mins by HTRF assay


Eur J Med Chem 138: 1158-1169 (2017)


Article DOI: 10.1016/j.ejmech.2017.07.046
BindingDB Entry DOI: 10.7270/Q2QC061V
More data for this
Ligand-Target Pair
Glucagon receptor


(Homo sapiens (Human))
BDBM50277061
PNG
(CHEMBL4159256)
Show SMILES CSCC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CS)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)Cc1cnc[nH]1)[C@@H](C)O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(N)=O |r|
Show InChI InChI=1S/C153H226N44O47S2/c1-72(2)52-97(134(227)177-96(47-51-246-11)133(226)185-104(60-115(159)209)144(237)196-121(76(8)201)124(160)217)180-138(231)103(58-83-64-168-89-29-19-18-28-87(83)89)184-132(225)95(43-46-114(158)208)178-149(242)120(74(5)6)195-142(235)101(54-79-24-14-12-15-25-79)183-139(232)105(61-117(211)212)186-131(224)94(42-45-113(157)207)172-125(218)75(7)171-128(221)91(31-22-49-166-152(161)162)173-129(222)92(32-23-50-167-153(163)164)175-148(241)111(70-245)193-141(234)107(63-119(215)216)187-135(228)98(53-73(3)4)179-136(229)99(56-81-33-37-85(204)38-34-81)181-130(223)90(30-20-21-48-154)174-146(239)109(68-199)191-137(230)100(57-82-35-39-86(205)40-36-82)182-140(233)106(62-118(213)214)188-147(240)110(69-200)192-151(244)123(78(10)203)197-143(236)102(55-80-26-16-13-17-27-80)189-150(243)122(77(9)202)194-116(210)66-169-127(220)93(41-44-112(156)206)176-145(238)108(67-198)190-126(219)88(155)59-84-65-165-71-170-84/h12-19,24-29,33-40,64-65,71-78,88,90-111,120-123,168,198-205,245H,20-23,30-32,41-63,66-70,154-155H2,1-11H3,(H2,156,206)(H2,157,207)(H2,158,208)(H2,159,209)(H2,160,217)(H,165,170)(H,169,220)(H,171,221)(H,172,218)(H,173,222)(H,174,239)(H,175,241)(H,176,238)(H,177,227)(H,178,242)(H,179,229)(H,180,231)(H,181,223)(H,182,233)(H,183,232)(H,184,225)(H,185,226)(H,186,224)(H,187,228)(H,188,240)(H,189,243)(H,190,219)(H,191,230)(H,192,244)(H,193,234)(H,194,210)(H,195,235)(H,196,237)(H,197,236)(H,211,212)(H,213,214)(H,215,216)(H4,161,162,166)(H4,163,164,167)/t75-,76+,77+,78+,88-,90-,91-,92-,93-,94-,95-,96-,97-,98-,99-,100-,101-,102-,103-,104-,105-,106-,107-,108-,109-,110-,111-,120-,121-,122-,123-/m0/s1
PDB
MMDB

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
KEGG
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 1.40n/an/an/an/a



China Pharmaceutical University

Curated by ChEMBL


Assay Description
Agonist activity at human GCGR expressed in HEK293 cells assessed as increase in cAMP accumulation after 20 mins by HTRF assay


Eur J Med Chem 138: 1158-1169 (2017)


Article DOI: 10.1016/j.ejmech.2017.07.046
BindingDB Entry DOI: 10.7270/Q2QC061V
More data for this
Ligand-Target Pair
Glucagon receptor


(Homo sapiens (Human))
BDBM50266668
PNG
(CHEMBL4098545)
Show SMILES CC[C@H](C)[C@H](NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CCCCN)NC(=O)[C@@H](NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CCSC)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CO)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)Cc1cnc[nH]1)[C@@H](C)O)[C@@H](C)O)C(C)C)[C@@H](C)O)C(=O)N[C@@H](C)C(O)=O |r|
Show InChI InChI=1S/C192H295N61O60S/c1-15-92(8)149(184(308)220-94(10)188(312)313)251-177(301)128(76-142(201)268)240-171(295)127(75-141(200)267)238-161(285)114(43-31-64-215-192(209)210)224-170(294)126(74-140(199)266)237-160(284)113(42-30-63-214-191(207)208)223-157(281)110(39-25-27-60-194)229-186(310)151(96(12)259)253-178(302)129(77-143(202)269)239-164(288)118(58-65-314-14)228-165(289)119(66-89(2)3)232-169(293)125(72-102-81-216-108-37-23-22-36-106(102)108)236-163(287)117(54-57-139(198)265)230-183(307)148(91(6)7)250-175(299)123(68-98-32-18-16-19-33-98)235-172(296)130(78-145(271)272)241-162(286)116(53-56-138(197)264)221-153(277)93(9)219-156(280)111(40-28-61-212-189(203)204)222-158(282)112(41-29-62-213-190(205)206)226-181(305)135(86-256)247-174(298)132(80-147(275)276)242-166(290)120(67-90(4)5)231-167(291)121(70-100-44-48-104(261)49-45-100)233-159(283)109(38-24-26-59-193)225-180(304)134(85-255)246-168(292)122(71-101-46-50-105(262)51-47-101)234-173(297)131(79-146(273)274)243-182(306)136(87-257)248-187(311)152(97(13)260)252-176(300)124(69-99-34-20-17-21-35-99)244-185(309)150(95(11)258)249-144(270)83-217-155(279)115(52-55-137(196)263)227-179(303)133(84-254)245-154(278)107(195)73-103-82-211-88-218-103/h16-23,32-37,44-51,81-82,88-97,107,109-136,148-152,216,254-262H,15,24-31,38-43,52-80,83-87,193-195H2,1-14H3,(H2,196,263)(H2,197,264)(H2,198,265)(H2,199,266)(H2,200,267)(H2,201,268)(H2,202,269)(H,211,218)(H,217,279)(H,219,280)(H,220,308)(H,221,277)(H,222,282)(H,223,281)(H,224,294)(H,225,304)(H,226,305)(H,227,303)(H,228,289)(H,229,310)(H,230,307)(H,231,291)(H,232,293)(H,233,283)(H,234,297)(H,235,296)(H,236,287)(H,237,284)(H,238,285)(H,239,288)(H,240,295)(H,241,286)(H,242,290)(H,243,306)(H,244,309)(H,245,278)(H,246,292)(H,247,298)(H,248,311)(H,249,270)(H,250,299)(H,251,301)(H,252,300)(H,253,302)(H,271,272)(H,273,274)(H,275,276)(H,312,313)(H4,203,204,212)(H4,205,206,213)(H4,207,208,214)(H4,209,210,215)/t92-,93-,94-,95+,96+,97+,107-,109-,110-,111-,112-,113-,114-,115-,116-,117-,118-,119-,120-,121-,122-,123-,124-,125-,126-,127-,128-,129-,130-,131-,132-,133-,134-,135-,136-,148-,149-,150-,151-,152-/m0/s1
PDB
MMDB

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
Purchase

PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 1.20n/an/an/an/a



China Pharmaceutical University

Curated by ChEMBL


Assay Description
Agonist activity at human GCGR expressed in HEK293 cells assessed as increase in cAMP accumulation after 20 mins by HTRF assay


Eur J Med Chem 138: 1158-1169 (2017)


Article DOI: 10.1016/j.ejmech.2017.07.046
BindingDB Entry DOI: 10.7270/Q2QC061V
More data for this
Ligand-Target Pair
Glucagon receptor


(Homo sapiens (Human))
BDBM50277062
PNG
(CHEMBL4175452)
Show SMILES CSCC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CO)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)Cc1cnc[nH]1)[C@@H](C)O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(N)=O |r|
Show InChI InChI=1S/C153H226N44O48S/c1-72(2)52-97(134(228)177-96(47-51-246-11)133(227)185-104(60-115(159)210)144(238)196-121(76(8)202)124(160)218)180-138(232)103(58-83-64-168-89-29-19-18-28-87(83)89)184-132(226)95(43-46-114(158)209)178-149(243)120(74(5)6)195-142(236)101(54-79-24-14-12-15-25-79)183-139(233)105(61-117(212)213)186-131(225)94(42-45-113(157)208)172-125(219)75(7)171-128(222)91(31-22-49-166-152(161)162)173-129(223)92(32-23-50-167-153(163)164)175-147(241)110(69-200)192-141(235)107(63-119(216)217)187-135(229)98(53-73(3)4)179-136(230)99(56-81-33-37-85(205)38-34-81)181-130(224)90(30-20-21-48-154)174-146(240)109(68-199)191-137(231)100(57-82-35-39-86(206)40-36-82)182-140(234)106(62-118(214)215)188-148(242)111(70-201)193-151(245)123(78(10)204)197-143(237)102(55-80-26-16-13-17-27-80)189-150(244)122(77(9)203)194-116(211)66-169-127(221)93(41-44-112(156)207)176-145(239)108(67-198)190-126(220)88(155)59-84-65-165-71-170-84/h12-19,24-29,33-40,64-65,71-78,88,90-111,120-123,168,198-206H,20-23,30-32,41-63,66-70,154-155H2,1-11H3,(H2,156,207)(H2,157,208)(H2,158,209)(H2,159,210)(H2,160,218)(H,165,170)(H,169,221)(H,171,222)(H,172,219)(H,173,223)(H,174,240)(H,175,241)(H,176,239)(H,177,228)(H,178,243)(H,179,230)(H,180,232)(H,181,224)(H,182,234)(H,183,233)(H,184,226)(H,185,227)(H,186,225)(H,187,229)(H,188,242)(H,189,244)(H,190,220)(H,191,231)(H,192,235)(H,193,245)(H,194,211)(H,195,236)(H,196,238)(H,197,237)(H,212,213)(H,214,215)(H,216,217)(H4,161,162,166)(H4,163,164,167)/t75-,76+,77+,78+,88-,90-,91-,92-,93-,94-,95-,96-,97-,98-,99-,100-,101-,102-,103-,104-,105-,106-,107-,108-,109-,110-,111-,120-,121-,122-,123-/m0/s1
PDB
MMDB

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Patents


Similars

Article
PubMed
n/an/an/an/a 1.70n/an/an/an/a



China Pharmaceutical University

Curated by ChEMBL


Assay Description
Agonist activity at human GCGR expressed in HEK293 cells assessed as increase in cAMP accumulation after 20 mins by HTRF assay


Eur J Med Chem 138: 1158-1169 (2017)


Article DOI: 10.1016/j.ejmech.2017.07.046
BindingDB Entry DOI: 10.7270/Q2QC061V
More data for this
Ligand-Target Pair
Glucagon-like peptide 1 receptor


(Homo sapiens (Human))
BDBM50277070
PNG
(CHEMBL4170976)
Show SMILES CCCCCCCCCCCCCCCCN1C(=O)CC(SC[C@H](NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CO)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)Cc2cnc[nH]2)[C@@H](C)O)[C@@H](C)O)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](Cc2ccccc2)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](Cc2c[nH]c3ccccc23)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(N)=O)C1=O |r|
Show InChI InChI=1S/C173H261N45O50S2/c1-12-13-14-15-16-17-18-19-20-21-22-23-24-35-65-218-135(233)79-129(171(218)268)270-87-128(167(264)195-110(56-59-131(177)229)149(246)205-121(76-136(234)235)157(254)202-117(69-95-38-27-25-28-39-95)160(257)215-139(91(6)7)168(265)197-111(57-60-132(178)230)150(247)203-119(73-99-80-188-105-43-32-31-42-103(99)105)156(253)199-113(67-89(2)3)152(249)196-112(61-66-269-11)151(248)204-120(75-133(179)231)162(259)216-140(92(8)223)143(180)240)213-148(245)108(46-37-64-187-173(183)184)191-146(243)107(45-36-63-186-172(181)182)193-165(262)126(85-221)211-159(256)123(78-138(238)239)206-153(250)114(68-90(4)5)198-154(251)115(71-97-47-51-101(226)52-48-97)200-147(244)106(44-33-34-62-174)192-164(261)125(84-220)210-155(252)116(72-98-49-53-102(227)54-50-98)201-158(255)122(77-137(236)237)207-166(263)127(86-222)212-170(267)142(94(10)225)217-161(258)118(70-96-40-29-26-30-41-96)208-169(266)141(93(9)224)214-134(232)82-189-145(242)109(55-58-130(176)228)194-163(260)124(83-219)209-144(241)104(175)74-100-81-185-88-190-100/h25-32,38-43,47-54,80-81,88-94,104,106-129,139-142,188,219-227H,12-24,33-37,44-46,55-79,82-87,174-175H2,1-11H3,(H2,176,228)(H2,177,229)(H2,178,230)(H2,179,231)(H2,180,240)(H,185,190)(H,189,242)(H,191,243)(H,192,261)(H,193,262)(H,194,260)(H,195,264)(H,196,249)(H,197,265)(H,198,251)(H,199,253)(H,200,244)(H,201,255)(H,202,254)(H,203,247)(H,204,248)(H,205,246)(H,206,250)(H,207,263)(H,208,266)(H,209,241)(H,210,252)(H,211,256)(H,212,267)(H,213,245)(H,214,232)(H,215,257)(H,216,259)(H,217,258)(H,234,235)(H,236,237)(H,238,239)(H4,181,182,186)(H4,183,184,187)/t92-,93-,94-,104+,106+,107+,108+,109+,110+,111+,112+,113+,114+,115+,116+,117+,118+,119+,120+,121+,122+,123+,124+,125+,126+,127+,128+,129?,139+,140+,141+,142+/m1/s1
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 112n/an/an/an/a



China Pharmaceutical University

Curated by ChEMBL


Assay Description
Agonist activity at full length human GLP1R expressed in HEK293 cells assessed as increase in cAMP accumulation after 20 mins by HTRF assay


Eur J Med Chem 138: 1158-1169 (2017)


Article DOI: 10.1016/j.ejmech.2017.07.046
BindingDB Entry DOI: 10.7270/Q2QC061V
More data for this
Ligand-Target Pair
Glucagon-like peptide 1 receptor


(Homo sapiens (Human))
BDBM50277071
PNG
(CHEMBL4160365)
Show SMILES CCCCCCCCCCCCN1C(=O)CC(SC[C@H](NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CO)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)Cc2cnc[nH]2)[C@@H](C)O)[C@@H](C)O)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](Cc2ccccc2)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](Cc2c[nH]c3ccccc23)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(N)=O)C1=O |r|
Show InChI InChI=1S/C169H253N45O50S2/c1-12-13-14-15-16-17-18-19-20-31-61-214-131(229)75-125(167(214)264)266-83-124(163(260)191-106(52-55-127(173)225)145(242)201-117(72-132(230)231)153(250)198-113(65-91-34-23-21-24-35-91)156(253)211-135(87(6)7)164(261)193-107(53-56-128(174)226)146(243)199-115(69-95-76-184-101-39-28-27-38-99(95)101)152(249)195-109(63-85(2)3)148(245)192-108(57-62-265-11)147(244)200-116(71-129(175)227)158(255)212-136(88(8)219)139(176)236)209-144(241)104(42-33-60-183-169(179)180)187-142(239)103(41-32-59-182-168(177)178)189-161(258)122(81-217)207-155(252)119(74-134(234)235)202-149(246)110(64-86(4)5)194-150(247)111(67-93-43-47-97(222)48-44-93)196-143(240)102(40-29-30-58-170)188-160(257)121(80-216)206-151(248)112(68-94-45-49-98(223)50-46-94)197-154(251)118(73-133(232)233)203-162(259)123(82-218)208-166(263)138(90(10)221)213-157(254)114(66-92-36-25-22-26-37-92)204-165(262)137(89(9)220)210-130(228)78-185-141(238)105(51-54-126(172)224)190-159(256)120(79-215)205-140(237)100(171)70-96-77-181-84-186-96/h21-28,34-39,43-50,76-77,84-90,100,102-125,135-138,184,215-223H,12-20,29-33,40-42,51-75,78-83,170-171H2,1-11H3,(H2,172,224)(H2,173,225)(H2,174,226)(H2,175,227)(H2,176,236)(H,181,186)(H,185,238)(H,187,239)(H,188,257)(H,189,258)(H,190,256)(H,191,260)(H,192,245)(H,193,261)(H,194,247)(H,195,249)(H,196,240)(H,197,251)(H,198,250)(H,199,243)(H,200,244)(H,201,242)(H,202,246)(H,203,259)(H,204,262)(H,205,237)(H,206,248)(H,207,252)(H,208,263)(H,209,241)(H,210,228)(H,211,253)(H,212,255)(H,213,254)(H,230,231)(H,232,233)(H,234,235)(H4,177,178,182)(H4,179,180,183)/t88-,89-,90-,100+,102+,103+,104+,105+,106+,107+,108+,109+,110+,111+,112+,113+,114+,115+,116+,117+,118+,119+,120+,121+,122+,123+,124+,125?,135+,136+,137+,138+/m1/s1
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Patents


Similars

Article
PubMed
n/an/an/an/a 29n/an/an/an/a



China Pharmaceutical University

Curated by ChEMBL


Assay Description
Agonist activity at full length human GLP1R expressed in HEK293 cells assessed as increase in cAMP accumulation after 20 mins by HTRF assay


Eur J Med Chem 138: 1158-1169 (2017)


Article DOI: 10.1016/j.ejmech.2017.07.046
BindingDB Entry DOI: 10.7270/Q2QC061V
More data for this
Ligand-Target Pair
Glucagon-like peptide 1 receptor


(Homo sapiens (Human))
BDBM50277063
PNG
(CHEMBL4163731)
Show SMILES CSCC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CSC1CC(=O)N(CCCCCCCCCCCC(O)=O)C1=O)NC(=O)[C@H](CO)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)Cc1cnc[nH]1)[C@@H](C)O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(N)=O |r|
Show InChI InChI=1S/C166H244N42O52S2/c1-82(2)60-106(146(241)186-105(55-59-261-11)145(240)194-113(68-126(172)221)156(251)206-134(86(8)213)137(173)232)189-150(245)112(66-93-73-178-99-37-27-26-36-97(93)99)193-144(239)104(51-54-125(171)220)187-162(257)133(84(5)6)205-154(249)110(62-89-32-21-19-22-33-89)192-151(246)114(69-130(226)227)195-143(238)103(50-53-124(170)219)182-138(233)85(7)181-141(236)101(39-31-57-177-166(174)175)184-161(256)121(80-262-122-72-128(223)208(165(122)260)58-30-18-16-14-12-13-15-17-25-40-129(224)225)203-160(255)119(78-211)201-153(248)116(71-132(230)231)196-147(242)107(61-83(3)4)188-148(243)108(64-91-41-45-95(216)46-42-91)190-142(237)100(38-28-29-56-167)183-158(253)118(77-210)200-149(244)109(65-92-43-47-96(217)48-44-92)191-152(247)115(70-131(228)229)197-159(254)120(79-212)202-164(259)136(88(10)215)207-155(250)111(63-90-34-23-20-24-35-90)198-163(258)135(87(9)214)204-127(222)75-179-140(235)102(49-52-123(169)218)185-157(252)117(76-209)199-139(234)98(168)67-94-74-176-81-180-94/h19-24,26-27,32-37,41-48,73-74,81-88,98,100-122,133-136,178,209-217H,12-18,25,28-31,38-40,49-72,75-80,167-168H2,1-11H3,(H2,169,218)(H2,170,219)(H2,171,220)(H2,172,221)(H2,173,232)(H,176,180)(H,179,235)(H,181,236)(H,182,233)(H,183,253)(H,184,256)(H,185,252)(H,186,241)(H,187,257)(H,188,243)(H,189,245)(H,190,237)(H,191,247)(H,192,246)(H,193,239)(H,194,240)(H,195,238)(H,196,242)(H,197,254)(H,198,258)(H,199,234)(H,200,244)(H,201,248)(H,202,259)(H,203,255)(H,204,222)(H,205,249)(H,206,251)(H,207,250)(H,224,225)(H,226,227)(H,228,229)(H,230,231)(H4,174,175,177)/t85-,86+,87+,88+,98-,100-,101-,102-,103-,104-,105-,106-,107-,108-,109-,110-,111-,112-,113-,114-,115-,116-,117-,118-,119-,120-,121-,122?,133-,134-,135-,136-/m0/s1
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Patents

Article
PubMed
n/an/an/an/a 3n/an/an/an/a



China Pharmaceutical University

Curated by ChEMBL


Assay Description
Agonist activity at full length human GLP1R expressed in HEK293 cells assessed as increase in cAMP accumulation after 20 mins by HTRF assay


Eur J Med Chem 138: 1158-1169 (2017)


Article DOI: 10.1016/j.ejmech.2017.07.046
BindingDB Entry DOI: 10.7270/Q2QC061V
More data for this
Ligand-Target Pair
Glucagon-like peptide 1 receptor


(Homo sapiens (Human))
BDBM50277081
PNG
(CHEMBL4162383)
Show SMILES CCCCCCN1C(=O)CC(SC[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)Cc2cnc[nH]2)[C@@H](C)O)[C@@H](C)O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](Cc2ccccc2)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](Cc2c[nH]c3ccccc23)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(N)=O)C1=O |r|
Show InChI InChI=1S/C160H234N42O50S2/c1-13-14-15-26-53-202-123(217)67-117(159(202)252)254-75-116(155(248)178-96(35-27-52-171-160(168)169)135(228)175-80(8)132(225)176-98(45-48-119(164)213)137(230)189-109(64-124(218)219)145(238)186-105(57-84-28-18-16-19-29-84)148(241)199-127(79(6)7)156(249)181-99(46-49-120(165)214)138(231)187-107(61-88-68-172-94-33-23-22-32-92(88)94)144(237)183-101(55-77(2)3)140(233)180-100(50-54-253-12)139(232)188-108(63-121(166)215)150(243)200-128(81(9)207)131(167)224)197-154(247)114(73-205)195-147(240)111(66-126(222)223)190-141(234)102(56-78(4)5)182-142(235)103(59-86-36-40-90(210)41-37-86)184-136(229)95(34-24-25-51-161)177-152(245)113(72-204)194-143(236)104(60-87-38-42-91(211)43-39-87)185-146(239)110(65-125(220)221)191-153(246)115(74-206)196-158(251)130(83(11)209)201-149(242)106(58-85-30-20-17-21-31-85)192-157(250)129(82(10)208)198-122(216)70-173-134(227)97(44-47-118(163)212)179-151(244)112(71-203)193-133(226)93(162)62-89-69-170-76-174-89/h16-23,28-33,36-43,68-69,76-83,93,95-117,127-130,172,203-211H,13-15,24-27,34-35,44-67,70-75,161-162H2,1-12H3,(H2,163,212)(H2,164,213)(H2,165,214)(H2,166,215)(H2,167,224)(H,170,174)(H,173,227)(H,175,228)(H,176,225)(H,177,245)(H,178,248)(H,179,244)(H,180,233)(H,181,249)(H,182,235)(H,183,237)(H,184,229)(H,185,239)(H,186,238)(H,187,231)(H,188,232)(H,189,230)(H,190,234)(H,191,246)(H,192,250)(H,193,226)(H,194,236)(H,195,240)(H,196,251)(H,197,247)(H,198,216)(H,199,241)(H,200,243)(H,201,242)(H,218,219)(H,220,221)(H,222,223)(H4,168,169,171)/t80-,81+,82+,83+,93-,95-,96-,97-,98-,99-,100-,101-,102-,103-,104-,105-,106-,107-,108-,109-,110-,111-,112-,113-,114-,115-,116-,117?,127-,128-,129-,130-/m0/s1
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 1.60n/an/an/an/a



China Pharmaceutical University

Curated by ChEMBL


Assay Description
Agonist activity at full length human GLP1R expressed in HEK293 cells assessed as increase in cAMP accumulation after 20 mins by HTRF assay


Eur J Med Chem 138: 1158-1169 (2017)


Article DOI: 10.1016/j.ejmech.2017.07.046
BindingDB Entry DOI: 10.7270/Q2QC061V
More data for this
Ligand-Target Pair
Glucagon-like peptide 1 receptor


(Homo sapiens (Human))
BDBM50277073
PNG
(CHEMBL4173061)
Show SMILES CSCC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CSC1CC(=O)N(CCCCCCCCCCCC(O)=O)C1=O)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)Cc1cnc[nH]1)[C@@H](C)O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(N)=O |r|
Show InChI InChI=1S/C169H251N45O51S2/c1-84(2)63-109(149(247)193-108(57-62-266-11)148(246)201-116(71-128(175)226)159(257)212-136(88(8)218)139(176)237)196-153(251)115(69-95-76-184-101-38-27-26-37-99(95)101)200-147(245)107(53-56-127(174)225)194-164(262)135(86(5)6)211-157(255)113(65-91-33-21-19-22-34-91)199-154(252)117(72-132(231)232)202-146(244)106(52-55-126(173)224)188-140(238)87(7)187-143(241)103(40-31-59-182-168(177)178)189-144(242)104(41-32-60-183-169(179)180)191-163(261)123(82-267-124-75-130(228)214(167(124)265)61-30-18-16-14-12-13-15-17-25-42-131(229)230)209-156(254)119(74-134(235)236)203-150(248)110(64-85(3)4)195-151(249)111(67-93-43-47-97(221)48-44-93)197-145(243)102(39-28-29-58-170)190-161(259)121(80-216)207-152(250)112(68-94-45-49-98(222)50-46-94)198-155(253)118(73-133(233)234)204-162(260)122(81-217)208-166(264)138(90(10)220)213-158(256)114(66-92-35-23-20-24-36-92)205-165(263)137(89(9)219)210-129(227)78-185-142(240)105(51-54-125(172)223)192-160(258)120(79-215)206-141(239)100(171)70-96-77-181-83-186-96/h19-24,26-27,33-38,43-50,76-77,83-90,100,102-124,135-138,184,215-222H,12-18,25,28-32,39-42,51-75,78-82,170-171H2,1-11H3,(H2,172,223)(H2,173,224)(H2,174,225)(H2,175,226)(H2,176,237)(H,181,186)(H,185,240)(H,187,241)(H,188,238)(H,189,242)(H,190,259)(H,191,261)(H,192,258)(H,193,247)(H,194,262)(H,195,249)(H,196,251)(H,197,243)(H,198,253)(H,199,252)(H,200,245)(H,201,246)(H,202,244)(H,203,248)(H,204,260)(H,205,263)(H,206,239)(H,207,250)(H,208,264)(H,209,254)(H,210,227)(H,211,255)(H,212,257)(H,213,256)(H,229,230)(H,231,232)(H,233,234)(H,235,236)(H4,177,178,182)(H4,179,180,183)/t87-,88+,89+,90+,100-,102-,103-,104-,105-,106-,107-,108-,109-,110-,111-,112-,113-,114-,115-,116-,117-,118-,119-,120-,121-,122-,123-,124?,135-,136-,137-,138-/m0/s1
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 0.860n/an/an/an/a



China Pharmaceutical University

Curated by ChEMBL


Assay Description
Agonist activity at full length human GLP1R expressed in HEK293 cells assessed as increase in cAMP accumulation after 20 mins by HTRF assay


Eur J Med Chem 138: 1158-1169 (2017)


Article DOI: 10.1016/j.ejmech.2017.07.046
BindingDB Entry DOI: 10.7270/Q2QC061V
More data for this
Ligand-Target Pair
Glucagon-like peptide 1 receptor


(Homo sapiens (Human))
BDBM50277082
PNG
(CHEMBL4159003)
Show SMILES CCCCCCCCCCCCCCCCN1C(=O)CC(SC[C@H](NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)Cc2cnc[nH]2)[C@@H](C)O)[C@@H](C)O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](Cc2ccccc2)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](Cc2c[nH]c3ccccc23)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(N)=O)C1=O |r|
Show InChI InChI=1S/C173H261N45O49S2/c1-13-14-15-16-17-18-19-20-21-22-23-24-25-36-66-218-135(232)80-129(171(218)267)269-87-128(167(263)195-109(47-38-65-187-173(183)184)148(244)193-108(46-37-64-186-172(181)182)147(243)191-92(8)144(240)192-111(57-60-131(177)228)150(246)206-122(77-136(233)234)158(254)203-118(70-96-39-28-26-29-40-96)161(257)215-139(91(6)7)168(264)198-112(58-61-132(178)229)151(247)204-120(74-100-81-188-106-44-33-32-43-104(100)106)157(253)200-114(68-89(2)3)153(249)197-113(62-67-268-12)152(248)205-121(76-133(179)230)163(259)216-140(93(9)222)143(180)239)213-160(256)124(79-138(237)238)207-154(250)115(69-90(4)5)199-155(251)116(72-98-48-52-102(225)53-49-98)201-149(245)107(45-34-35-63-174)194-165(261)126(85-220)211-156(252)117(73-99-50-54-103(226)55-51-99)202-159(255)123(78-137(235)236)208-166(262)127(86-221)212-170(266)142(95(11)224)217-162(258)119(71-97-41-30-27-31-42-97)209-169(265)141(94(10)223)214-134(231)83-189-146(242)110(56-59-130(176)227)196-164(260)125(84-219)210-145(241)105(175)75-101-82-185-88-190-101/h26-33,39-44,48-55,81-82,88-95,105,107-129,139-142,188,219-226H,13-25,34-38,45-47,56-80,83-87,174-175H2,1-12H3,(H2,176,227)(H2,177,228)(H2,178,229)(H2,179,230)(H2,180,239)(H,185,190)(H,189,242)(H,191,243)(H,192,240)(H,193,244)(H,194,261)(H,195,263)(H,196,260)(H,197,249)(H,198,264)(H,199,251)(H,200,253)(H,201,245)(H,202,255)(H,203,254)(H,204,247)(H,205,248)(H,206,246)(H,207,250)(H,208,262)(H,209,265)(H,210,241)(H,211,252)(H,212,266)(H,213,256)(H,214,231)(H,215,257)(H,216,259)(H,217,258)(H,233,234)(H,235,236)(H,237,238)(H4,181,182,186)(H4,183,184,187)/t92-,93+,94+,95+,105-,107-,108-,109-,110-,111-,112-,113-,114-,115-,116-,117-,118-,119-,120-,121-,122-,123-,124-,125-,126-,127-,128-,129?,139-,140-,141-,142-/m0/s1
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 88n/an/an/an/a



China Pharmaceutical University

Curated by ChEMBL


Assay Description
Agonist activity at full length human GLP1R expressed in HEK293 cells assessed as increase in cAMP accumulation after 20 mins by HTRF assay


Eur J Med Chem 138: 1158-1169 (2017)


Article DOI: 10.1016/j.ejmech.2017.07.046
BindingDB Entry DOI: 10.7270/Q2QC061V
More data for this
Ligand-Target Pair
Glucagon-like peptide 1 receptor


(Homo sapiens (Human))
BDBM50277057
PNG
(CHEMBL4174154)
Show SMILES CCCCCCN1C(=O)CC(SC[C@H](NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)Cc2cnc[nH]2)[C@@H](C)O)[C@@H](C)O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](Cc2ccccc2)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](Cc2c[nH]c3ccccc23)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(N)=O)C1=O |r|
Show InChI InChI=1S/C163H241N45O49S2/c1-13-14-15-26-56-208-125(222)70-119(161(208)257)259-77-118(157(253)185-99(37-28-55-177-163(173)174)138(234)183-98(36-27-54-176-162(171)172)137(233)181-82(8)134(230)182-101(47-50-121(167)218)140(236)196-112(67-126(223)224)148(244)193-108(60-86-29-18-16-19-30-86)151(247)205-129(81(6)7)158(254)188-102(48-51-122(168)219)141(237)194-110(64-90-71-178-96-34-23-22-33-94(90)96)147(243)190-104(58-79(2)3)143(239)187-103(52-57-258-12)142(238)195-111(66-123(169)220)153(249)206-130(83(9)212)133(170)229)203-150(246)114(69-128(227)228)197-144(240)105(59-80(4)5)189-145(241)106(62-88-38-42-92(215)43-39-88)191-139(235)97(35-24-25-53-164)184-155(251)116(75-210)201-146(242)107(63-89-40-44-93(216)45-41-89)192-149(245)113(68-127(225)226)198-156(252)117(76-211)202-160(256)132(85(11)214)207-152(248)109(61-87-31-20-17-21-32-87)199-159(255)131(84(10)213)204-124(221)73-179-136(232)100(46-49-120(166)217)186-154(250)115(74-209)200-135(231)95(165)65-91-72-175-78-180-91/h16-23,29-34,38-45,71-72,78-85,95,97-119,129-132,178,209-216H,13-15,24-28,35-37,46-70,73-77,164-165H2,1-12H3,(H2,166,217)(H2,167,218)(H2,168,219)(H2,169,220)(H2,170,229)(H,175,180)(H,179,232)(H,181,233)(H,182,230)(H,183,234)(H,184,251)(H,185,253)(H,186,250)(H,187,239)(H,188,254)(H,189,241)(H,190,243)(H,191,235)(H,192,245)(H,193,244)(H,194,237)(H,195,238)(H,196,236)(H,197,240)(H,198,252)(H,199,255)(H,200,231)(H,201,242)(H,202,256)(H,203,246)(H,204,221)(H,205,247)(H,206,249)(H,207,248)(H,223,224)(H,225,226)(H,227,228)(H4,171,172,176)(H4,173,174,177)/t82-,83+,84+,85+,95-,97-,98-,99-,100-,101-,102-,103-,104-,105-,106-,107-,108-,109-,110-,111-,112-,113-,114-,115-,116-,117-,118-,119?,129-,130-,131-,132-/m0/s1
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 3.30n/an/an/an/a



China Pharmaceutical University

Curated by ChEMBL


Assay Description
Agonist activity at full length human GLP1R expressed in HEK293 cells assessed as increase in cAMP accumulation after 20 mins by HTRF assay


Eur J Med Chem 138: 1158-1169 (2017)


Article DOI: 10.1016/j.ejmech.2017.07.046
BindingDB Entry DOI: 10.7270/Q2QC061V
More data for this
Ligand-Target Pair
Glucagon-like peptide 1 receptor


(Homo sapiens (Human))
BDBM50277074
PNG
(CHEMBL4166241)
Show SMILES CSCC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CS)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CO)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)Cc1cnc[nH]1)[C@@H](C)O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(N)=O |r|
Show InChI InChI=1S/C151H223N43O47S2/c1-71(2)50-95(131(223)174-94(45-49-243-11)130(222)181-102(58-113(156)206)141(233)193-119(75(8)199)122(157)214)176-135(227)101(56-82-62-165-88-29-19-18-28-86(82)88)180-146(238)110(69-242)190-147(239)118(73(5)6)192-139(231)99(52-78-24-14-12-15-25-78)179-136(228)103(59-115(208)209)182-129(221)93(42-44-112(155)205)169-123(215)74(7)168-126(218)90(31-22-47-163-150(158)159)170-127(219)91(32-23-48-164-151(160)161)172-144(236)108(67-197)188-138(230)105(61-117(212)213)183-132(224)96(51-72(3)4)175-133(225)97(54-80-33-37-84(202)38-34-80)177-128(220)89(30-20-21-46-152)171-143(235)107(66-196)187-134(226)98(55-81-35-39-85(203)40-36-81)178-137(229)104(60-116(210)211)184-145(237)109(68-198)189-149(241)121(77(10)201)194-140(232)100(53-79-26-16-13-17-27-79)185-148(240)120(76(9)200)191-114(207)64-166-125(217)92(41-43-111(154)204)173-142(234)106(65-195)186-124(216)87(153)57-83-63-162-70-167-83/h12-19,24-29,33-40,62-63,70-77,87,89-110,118-121,165,195-203,242H,20-23,30-32,41-61,64-69,152-153H2,1-11H3,(H2,154,204)(H2,155,205)(H2,156,206)(H2,157,214)(H,162,167)(H,166,217)(H,168,218)(H,169,215)(H,170,219)(H,171,235)(H,172,236)(H,173,234)(H,174,223)(H,175,225)(H,176,227)(H,177,220)(H,178,229)(H,179,228)(H,180,238)(H,181,222)(H,182,221)(H,183,224)(H,184,237)(H,185,240)(H,186,216)(H,187,226)(H,188,230)(H,189,241)(H,190,239)(H,191,207)(H,192,231)(H,193,233)(H,194,232)(H,208,209)(H,210,211)(H,212,213)(H4,158,159,163)(H4,160,161,164)/t74-,75+,76+,77+,87-,89-,90-,91-,92-,93-,94-,95-,96-,97-,98-,99-,100-,101-,102-,103-,104-,105-,106-,107-,108-,109-,110-,118-,119-,120-,121-/m0/s1
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
KEGG
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 3.60n/an/an/an/a



China Pharmaceutical University

Curated by ChEMBL


Assay Description
Agonist activity at full length human GLP1R expressed in HEK293 cells assessed as increase in cAMP accumulation after 20 mins by HTRF assay


Eur J Med Chem 138: 1158-1169 (2017)


Article DOI: 10.1016/j.ejmech.2017.07.046
BindingDB Entry DOI: 10.7270/Q2QC061V
More data for this
Ligand-Target Pair
Glucagon-like peptide 1 receptor


(Homo sapiens (Human))
BDBM50277083
PNG
(CHEMBL4159426)
Show SMILES CSCC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CS)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CO)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)Cc1cnc[nH]1)[C@@H](C)O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(N)=O |r|
Show InChI InChI=1S/C151H223N43O47S2/c1-71(2)50-95(131(223)173-94(45-49-243-11)130(222)181-102(58-113(156)206)141(233)193-119(75(8)199)122(157)214)176-135(227)101(56-82-62-165-88-29-19-18-28-86(82)88)180-129(221)93(42-44-112(155)205)174-147(239)118(73(5)6)192-139(231)99(52-78-24-14-12-15-25-78)179-137(229)104(60-116(210)211)184-146(238)110(69-242)190-123(215)74(7)168-126(218)90(31-22-47-163-150(158)159)169-127(219)91(32-23-48-164-151(160)161)171-144(236)108(67-197)188-138(230)105(61-117(212)213)182-132(224)96(51-72(3)4)175-133(225)97(54-80-33-37-84(202)38-34-80)177-128(220)89(30-20-21-46-152)170-143(235)107(66-196)187-134(226)98(55-81-35-39-85(203)40-36-81)178-136(228)103(59-115(208)209)183-145(237)109(68-198)189-149(241)121(77(10)201)194-140(232)100(53-79-26-16-13-17-27-79)185-148(240)120(76(9)200)191-114(207)64-166-125(217)92(41-43-111(154)204)172-142(234)106(65-195)186-124(216)87(153)57-83-63-162-70-167-83/h12-19,24-29,33-40,62-63,70-77,87,89-110,118-121,165,195-203,242H,20-23,30-32,41-61,64-69,152-153H2,1-11H3,(H2,154,204)(H2,155,205)(H2,156,206)(H2,157,214)(H,162,167)(H,166,217)(H,168,218)(H,169,219)(H,170,235)(H,171,236)(H,172,234)(H,173,223)(H,174,239)(H,175,225)(H,176,227)(H,177,220)(H,178,228)(H,179,229)(H,180,221)(H,181,222)(H,182,224)(H,183,237)(H,184,238)(H,185,240)(H,186,216)(H,187,226)(H,188,230)(H,189,241)(H,190,215)(H,191,207)(H,192,231)(H,193,233)(H,194,232)(H,208,209)(H,210,211)(H,212,213)(H4,158,159,163)(H4,160,161,164)/t74-,75+,76+,77+,87-,89-,90-,91-,92-,93-,94-,95-,96-,97-,98-,99-,100-,101-,102-,103-,104-,105-,106-,107-,108-,109-,110-,118-,119-,120-,121-/m0/s1
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
KEGG
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 32n/an/an/an/a



China Pharmaceutical University

Curated by ChEMBL


Assay Description
Agonist activity at full length human GLP1R expressed in HEK293 cells assessed as increase in cAMP accumulation after 20 mins by HTRF assay


Eur J Med Chem 138: 1158-1169 (2017)


Article DOI: 10.1016/j.ejmech.2017.07.046
BindingDB Entry DOI: 10.7270/Q2QC061V
More data for this
Ligand-Target Pair
Glucagon-like peptide 1 receptor


(Homo sapiens (Human))
BDBM50277080
PNG
(CHEMBL4172444)
Show SMILES CSCC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](CS)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CO)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)Cc1cnc[nH]1)[C@@H](C)O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(N)=O |r|
Show InChI InChI=1S/C150H219N41O48S2/c1-70(2)49-94(131(221)170-93(45-48-241-11)130(220)178-101(57-113(156)204)141(231)190-119(74(8)196)122(157)212)173-135(225)100(55-81-61-162-87-28-19-18-27-85(81)87)177-129(219)92(41-44-112(155)203)171-147(237)118(72(5)6)189-139(229)98(51-77-23-14-12-15-24-77)176-136(226)102(58-115(206)207)179-128(218)91(40-43-111(154)202)166-123(213)73(7)165-146(236)109(68-240)187-127(217)89(30-22-47-161-150(158)159)168-144(234)107(66-194)185-138(228)104(60-117(210)211)180-132(222)95(50-71(3)4)172-133(223)96(53-79-31-35-83(199)36-32-79)174-126(216)88(29-20-21-46-151)167-143(233)106(65-193)184-134(224)97(54-80-33-37-84(200)38-34-80)175-137(227)103(59-116(208)209)181-145(235)108(67-195)186-149(239)121(76(10)198)191-140(230)99(52-78-25-16-13-17-26-78)182-148(238)120(75(9)197)188-114(205)63-163-125(215)90(39-42-110(153)201)169-142(232)105(64-192)183-124(214)86(152)56-82-62-160-69-164-82/h12-19,23-28,31-38,61-62,69-76,86,88-109,118-121,162,192-200,240H,20-22,29-30,39-60,63-68,151-152H2,1-11H3,(H2,153,201)(H2,154,202)(H2,155,203)(H2,156,204)(H2,157,212)(H,160,164)(H,163,215)(H,165,236)(H,166,213)(H,167,233)(H,168,234)(H,169,232)(H,170,221)(H,171,237)(H,172,223)(H,173,225)(H,174,216)(H,175,227)(H,176,226)(H,177,219)(H,178,220)(H,179,218)(H,180,222)(H,181,235)(H,182,238)(H,183,214)(H,184,224)(H,185,228)(H,186,239)(H,187,217)(H,188,205)(H,189,229)(H,190,231)(H,191,230)(H,206,207)(H,208,209)(H,210,211)(H4,158,159,161)/t73-,74+,75+,76+,86-,88-,89-,90-,91-,92-,93-,94-,95-,96-,97-,98-,99-,100-,101-,102-,103-,104-,105-,106-,107-,108-,109-,118-,119-,120-,121-/m0/s1
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
KEGG
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 16n/an/an/an/a



China Pharmaceutical University

Curated by ChEMBL


Assay Description
Agonist activity at full length human GLP1R expressed in HEK293 cells assessed as increase in cAMP accumulation after 20 mins by HTRF assay


Eur J Med Chem 138: 1158-1169 (2017)


Article DOI: 10.1016/j.ejmech.2017.07.046
BindingDB Entry DOI: 10.7270/Q2QC061V
More data for this
Ligand-Target Pair
Glucagon-like peptide 1 receptor


(Homo sapiens (Human))
BDBM50277068
PNG
(CHEMBL4167169)
Show SMILES CSCC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CS)NC(=O)[C@H](CO)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)Cc1cnc[nH]1)[C@@H](C)O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(N)=O |r|
Show InChI InChI=1S/C150H219N41O48S2/c1-70(2)49-94(131(221)170-93(45-48-241-11)130(220)178-101(57-113(156)204)141(231)190-119(74(8)196)122(157)212)173-135(225)100(55-81-61-162-87-28-19-18-27-85(81)87)177-129(219)92(41-44-112(155)203)171-147(237)118(72(5)6)189-139(229)98(51-77-23-14-12-15-24-77)176-136(226)102(58-115(206)207)179-128(218)91(40-43-111(154)202)166-123(213)73(7)165-126(216)89(30-22-47-161-150(158)159)168-146(236)109(68-240)187-145(235)107(66-194)185-138(228)104(60-117(210)211)180-132(222)95(50-71(3)4)172-133(223)96(53-79-31-35-83(199)36-32-79)174-127(217)88(29-20-21-46-151)167-143(233)106(65-193)184-134(224)97(54-80-33-37-84(200)38-34-80)175-137(227)103(59-116(208)209)181-144(234)108(67-195)186-149(239)121(76(10)198)191-140(230)99(52-78-25-16-13-17-26-78)182-148(238)120(75(9)197)188-114(205)63-163-125(215)90(39-42-110(153)201)169-142(232)105(64-192)183-124(214)86(152)56-82-62-160-69-164-82/h12-19,23-28,31-38,61-62,69-76,86,88-109,118-121,162,192-200,240H,20-22,29-30,39-60,63-68,151-152H2,1-11H3,(H2,153,201)(H2,154,202)(H2,155,203)(H2,156,204)(H2,157,212)(H,160,164)(H,163,215)(H,165,216)(H,166,213)(H,167,233)(H,168,236)(H,169,232)(H,170,221)(H,171,237)(H,172,223)(H,173,225)(H,174,217)(H,175,227)(H,176,226)(H,177,219)(H,178,220)(H,179,218)(H,180,222)(H,181,234)(H,182,238)(H,183,214)(H,184,224)(H,185,228)(H,186,239)(H,187,235)(H,188,205)(H,189,229)(H,190,231)(H,191,230)(H,206,207)(H,208,209)(H,210,211)(H4,158,159,161)/t73-,74+,75+,76+,86-,88-,89-,90-,91-,92-,93-,94-,95-,96-,97-,98-,99-,100-,101-,102-,103-,104-,105-,106-,107-,108-,109-,118-,119-,120-,121-/m0/s1
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
KEGG
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 1.80n/an/an/an/a



China Pharmaceutical University

Curated by ChEMBL


Assay Description
Agonist activity at full length human GLP1R expressed in HEK293 cells assessed as increase in cAMP accumulation after 20 mins by HTRF assay


Eur J Med Chem 138: 1158-1169 (2017)


Article DOI: 10.1016/j.ejmech.2017.07.046
BindingDB Entry DOI: 10.7270/Q2QC061V
More data for this
Ligand-Target Pair
Glucagon-like peptide 1 receptor


(Homo sapiens (Human))
BDBM50277056
PNG
(CHEMBL4163714)
Show SMILES CSCC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CO)NC(=O)[C@H](CS)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)Cc1cnc[nH]1)[C@@H](C)O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(N)=O |r|
Show InChI InChI=1S/C152H226N44O46S2/c1-72(2)52-97(133(225)176-96(47-51-244-11)132(224)184-104(60-115(158)209)142(234)195-120(76(8)201)123(159)215)179-137(229)103(58-83-63-167-89-29-19-18-28-87(83)89)183-131(223)95(43-46-114(157)208)177-148(240)119(74(5)6)194-140(232)101(54-79-24-14-12-15-25-79)182-138(230)105(61-117(211)212)185-130(222)94(42-45-113(156)207)171-124(216)75(7)170-127(219)91(31-22-49-165-151(160)161)172-128(220)92(32-23-50-166-152(162)163)174-145(237)109(68-199)190-147(239)111(70-243)192-134(226)98(53-73(3)4)178-135(227)99(56-81-33-37-85(204)38-34-81)180-129(221)90(30-20-21-48-153)173-144(236)108(67-198)189-136(228)100(57-82-35-39-86(205)40-36-82)181-139(231)106(62-118(213)214)186-146(238)110(69-200)191-150(242)122(78(10)203)196-141(233)102(55-80-26-16-13-17-27-80)187-149(241)121(77(9)202)193-116(210)65-168-126(218)93(41-44-112(155)206)175-143(235)107(66-197)188-125(217)88(154)59-84-64-164-71-169-84/h12-19,24-29,33-40,63-64,71-78,88,90-111,119-122,167,197-205,243H,20-23,30-32,41-62,65-70,153-154H2,1-11H3,(H2,155,206)(H2,156,207)(H2,157,208)(H2,158,209)(H2,159,215)(H,164,169)(H,168,218)(H,170,219)(H,171,216)(H,172,220)(H,173,236)(H,174,237)(H,175,235)(H,176,225)(H,177,240)(H,178,227)(H,179,229)(H,180,221)(H,181,231)(H,182,230)(H,183,223)(H,184,224)(H,185,222)(H,186,238)(H,187,241)(H,188,217)(H,189,228)(H,190,239)(H,191,242)(H,192,226)(H,193,210)(H,194,232)(H,195,234)(H,196,233)(H,211,212)(H,213,214)(H4,160,161,165)(H4,162,163,166)/t75-,76+,77+,78+,88-,90-,91-,92-,93-,94-,95-,96-,97-,98-,99-,100-,101-,102-,103-,104-,105-,106-,107-,108-,109-,110-,111-,119-,120-,121-,122-/m0/s1
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
KEGG
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 1.40n/an/an/an/a



China Pharmaceutical University

Curated by ChEMBL


Assay Description
Agonist activity at full length human GLP1R expressed in HEK293 cells assessed as increase in cAMP accumulation after 20 mins by HTRF assay


Eur J Med Chem 138: 1158-1169 (2017)


Article DOI: 10.1016/j.ejmech.2017.07.046
BindingDB Entry DOI: 10.7270/Q2QC061V
More data for this
Ligand-Target Pair
Glucagon-like peptide 1 receptor


(Homo sapiens (Human))
BDBM50277084
PNG
(CHEMBL4160347)
Show SMILES CSCC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CO)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CS)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)Cc1cnc[nH]1)[C@@H](C)O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(N)=O |r|
Show InChI InChI=1S/C147H222N44O47S2/c1-68(2)48-91(128(221)171-90(43-47-240-11)127(220)178-97(55-109(153)203)137(230)190-115(72(8)196)118(154)211)173-131(224)96(53-78-59-162-83-29-19-18-28-81(78)83)177-126(219)89(39-42-108(152)202)172-143(236)114(70(5)6)189-135(228)94(50-75-24-14-12-15-25-75)176-132(225)98(56-111(205)206)179-125(218)88(38-41-107(151)201)166-119(212)71(7)165-122(215)85(31-22-45-160-146(155)156)167-123(216)86(32-23-46-161-147(157)158)169-140(233)103(64-194)185-134(227)100(58-113(209)210)180-129(222)92(49-69(3)4)174-142(235)105(66-239)187-124(217)84(30-20-21-44-148)168-139(232)102(63-193)184-130(223)93(52-77-33-35-80(199)36-34-77)175-133(226)99(57-112(207)208)181-141(234)104(65-195)186-145(238)117(74(10)198)191-136(229)95(51-76-26-16-13-17-27-76)182-144(237)116(73(9)197)188-110(204)61-163-121(214)87(37-40-106(150)200)170-138(231)101(62-192)183-120(213)82(149)54-79-60-159-67-164-79/h12-19,24-29,33-36,59-60,67-74,82,84-105,114-117,162,192-199,239H,20-23,30-32,37-58,61-66,148-149H2,1-11H3,(H2,150,200)(H2,151,201)(H2,152,202)(H2,153,203)(H2,154,211)(H,159,164)(H,163,214)(H,165,215)(H,166,212)(H,167,216)(H,168,232)(H,169,233)(H,170,231)(H,171,221)(H,172,236)(H,173,224)(H,174,235)(H,175,226)(H,176,225)(H,177,219)(H,178,220)(H,179,218)(H,180,222)(H,181,234)(H,182,237)(H,183,213)(H,184,223)(H,185,227)(H,186,238)(H,187,217)(H,188,204)(H,189,228)(H,190,230)(H,191,229)(H,205,206)(H,207,208)(H,209,210)(H4,155,156,160)(H4,157,158,161)/t71-,72+,73+,74+,82-,84-,85-,86-,87-,88-,89-,90-,91-,92-,93-,94-,95-,96-,97-,98-,99-,100-,101-,102-,103-,104-,105-,114-,115-,116-,117-/m0/s1
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
KEGG
PC cid
PC sid
UniChem
Article
PubMed
n/an/an/an/a 10n/an/an/an/a



China Pharmaceutical University

Curated by ChEMBL


Assay Description
Agonist activity at full length human GLP1R expressed in HEK293 cells assessed as increase in cAMP accumulation after 20 mins by HTRF assay


Eur J Med Chem 138: 1158-1169 (2017)


Article DOI: 10.1016/j.ejmech.2017.07.046
BindingDB Entry DOI: 10.7270/Q2QC061V
More data for this
Ligand-Target Pair
Glucagon-like peptide 1 receptor


(Homo sapiens (Human))
BDBM50266668
PNG
(CHEMBL4098545)
Show SMILES CC[C@H](C)[C@H](NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CCCCN)NC(=O)[C@@H](NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CCSC)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CO)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)Cc1cnc[nH]1)[C@@H](C)O)[C@@H](C)O)C(C)C)[C@@H](C)O)C(=O)N[C@@H](C)C(O)=O |r|
Show InChI InChI=1S/C192H295N61O60S/c1-15-92(8)149(184(308)220-94(10)188(312)313)251-177(301)128(76-142(201)268)240-171(295)127(75-141(200)267)238-161(285)114(43-31-64-215-192(209)210)224-170(294)126(74-140(199)266)237-160(284)113(42-30-63-214-191(207)208)223-157(281)110(39-25-27-60-194)229-186(310)151(96(12)259)253-178(302)129(77-143(202)269)239-164(288)118(58-65-314-14)228-165(289)119(66-89(2)3)232-169(293)125(72-102-81-216-108-37-23-22-36-106(102)108)236-163(287)117(54-57-139(198)265)230-183(307)148(91(6)7)250-175(299)123(68-98-32-18-16-19-33-98)235-172(296)130(78-145(271)272)241-162(286)116(53-56-138(197)264)221-153(277)93(9)219-156(280)111(40-28-61-212-189(203)204)222-158(282)112(41-29-62-213-190(205)206)226-181(305)135(86-256)247-174(298)132(80-147(275)276)242-166(290)120(67-90(4)5)231-167(291)121(70-100-44-48-104(261)49-45-100)233-159(283)109(38-24-26-59-193)225-180(304)134(85-255)246-168(292)122(71-101-46-50-105(262)51-47-101)234-173(297)131(79-146(273)274)243-182(306)136(87-257)248-187(311)152(97(13)260)252-176(300)124(69-99-34-20-17-21-35-99)244-185(309)150(95(11)258)249-144(270)83-217-155(279)115(52-55-137(196)263)227-179(303)133(84-254)245-154(278)107(195)73-103-82-211-88-218-103/h16-23,32-37,44-51,81-82,88-97,107,109-136,148-152,216,254-262H,15,24-31,38-43,52-80,83-87,193-195H2,1-14H3,(H2,196,263)(H2,197,264)(H2,198,265)(H2,199,266)(H2,200,267)(H2,201,268)(H2,202,269)(H,211,218)(H,217,279)(H,219,280)(H,220,308)(H,221,277)(H,222,282)(H,223,281)(H,224,294)(H,225,304)(H,226,305)(H,227,303)(H,228,289)(H,229,310)(H,230,307)(H,231,291)(H,232,293)(H,233,283)(H,234,297)(H,235,296)(H,236,287)(H,237,284)(H,238,285)(H,239,288)(H,240,295)(H,241,286)(H,242,290)(H,243,306)(H,244,309)(H,245,278)(H,246,292)(H,247,298)(H,248,311)(H,249,270)(H,250,299)(H,251,301)(H,252,300)(H,253,302)(H,271,272)(H,273,274)(H,275,276)(H,312,313)(H4,203,204,212)(H4,205,206,213)(H4,207,208,214)(H4,209,210,215)/t92-,93-,94-,95+,96+,97+,107-,109-,110-,111-,112-,113-,114-,115-,116-,117-,118-,119-,120-,121-,122-,123-,124-,125-,126-,127-,128-,129-,130-,131-,132-,133-,134-,135-,136-,148-,149-,150-,151-,152-/m0/s1
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
Purchase

PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 12n/an/an/an/a



China Pharmaceutical University

Curated by ChEMBL


Assay Description
Agonist activity at full length human GLP1R expressed in HEK293 cells assessed as increase in cAMP accumulation after 20 mins by HTRF assay


Eur J Med Chem 138: 1158-1169 (2017)


Article DOI: 10.1016/j.ejmech.2017.07.046
BindingDB Entry DOI: 10.7270/Q2QC061V
More data for this
Ligand-Target Pair
Glucagon-like peptide 1 receptor


(Homo sapiens (Human))
BDBM50266693
PNG
(CHEBI:5391 | Glucagen Hypokit | Glucagon | Glucago...)
Show SMILES CSCC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CO)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)Cc1c[nH]cn1)[C@@H](C)O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(O)=O
Show InChI InChI=1S/C153H225N43O49S/c1-72(2)52-97(133(226)176-96(47-51-246-11)132(225)184-104(60-115(159)209)143(236)196-123(78(10)203)151(244)245)179-137(230)103(58-83-64-167-89-29-19-18-28-87(83)89)183-131(224)95(43-46-114(158)208)177-148(241)120(74(5)6)194-141(234)101(54-79-24-14-12-15-25-79)182-138(231)105(61-117(211)212)185-130(223)94(42-45-113(157)207)171-124(217)75(7)170-127(220)91(31-22-49-165-152(160)161)172-128(221)92(32-23-50-166-153(162)163)174-146(239)110(69-199)191-140(233)107(63-119(215)216)186-134(227)98(53-73(3)4)178-135(228)99(56-81-33-37-85(204)38-34-81)180-129(222)90(30-20-21-48-154)173-145(238)109(68-198)190-136(229)100(57-82-35-39-86(205)40-36-82)181-139(232)106(62-118(213)214)187-147(240)111(70-200)192-150(243)122(77(9)202)195-142(235)102(55-80-26-16-13-17-27-80)188-149(242)121(76(8)201)193-116(210)66-168-126(219)93(41-44-112(156)206)175-144(237)108(67-197)189-125(218)88(155)59-84-65-164-71-169-84/h12-19,24-29,33-40,64-65,71-78,88,90-111,120-123,167,197-205H,20-23,30-32,41-63,66-70,154-155H2,1-11H3,(H2,156,206)(H2,157,207)(H2,158,208)(H2,159,209)(H,164,169)(H,168,219)(H,170,220)(H,171,217)(H,172,221)(H,173,238)(H,174,239)(H,175,237)(H,176,226)(H,177,241)(H,178,228)(H,179,230)(H,180,222)(H,181,232)(H,182,231)(H,183,224)(H,184,225)(H,185,223)(H,186,227)(H,187,240)(H,188,242)(H,189,218)(H,190,229)(H,191,233)(H,192,243)(H,193,210)(H,194,234)(H,195,235)(H,196,236)(H,211,212)(H,213,214)(H,215,216)(H,244,245)(H4,160,161,165)(H4,162,163,166)/t75-,76+,77+,78+,88-,90-,91-,92-,93-,94-,95-,96-,97-,98-,99-,100-,101-,102-,103-,104-,105-,106-,107-,108-,109-,110-,111-,120-,121-,122-,123-/m0/s1
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 7.70n/an/an/an/a



China Pharmaceutical University

Curated by ChEMBL


Assay Description
Agonist activity at full length human GLP1R expressed in HEK293 cells assessed as increase in cAMP accumulation after 20 mins by HTRF assay


Eur J Med Chem 138: 1158-1169 (2017)


Article DOI: 10.1016/j.ejmech.2017.07.046
BindingDB Entry DOI: 10.7270/Q2QC061V
More data for this
Ligand-Target Pair
Glucagon-like peptide 1 receptor


(Homo sapiens (Human))
BDBM50121518
PNG
(CHEMBL428139)
Show SMILES CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)CNC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](C)NC(=O)[C@@H](N)Cc1c[nH]cn1)[C@@H](C)O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCCCN)C(=O)NCC(=O)N[C@@H](CCCN=C(N)N)C(=O)NCC(O)=O |wU:119.121,95.99,89.93,105.111,142.150,8.16,195.200,134.137,69.74,28.34,210.215,223.228,156.159,164.169,167.172,42.43,176.180,2.2,wD:113.117,123.133,101.103,203.208,4.4,181.184,77.87,19.25,47.53,60.66,37.38,151.154,(42.46,-37.33,;42.37,-38.87,;40.99,-39.57,;39.7,-38.74,;40.89,-41.1,;42.2,-41.97,;43.56,-41.27,;43.68,-39.74,;44.87,-42.13,;44.77,-43.67,;43.39,-44.36,;42.09,-43.51,;40.71,-44.19,;40.63,-45.74,;41.92,-46.56,;43.3,-45.88,;46.26,-41.41,;48.15,-38.22,;50.19,-38.22,;47.05,-35.91,;45.48,-36.01,;44.58,-34.7,;43,-34.7,;42.23,-33.32,;42.2,-36.08,;47.71,-34.5,;46.82,-33.25,;45.29,-33.35,;47.5,-31.88,;49.02,-31.71,;49.9,-33.02,;51.45,-32.86,;52.3,-34.13,;53.88,-34.01,;46.61,-30.57,;47.28,-29.18,;48.81,-29.04,;46.4,-27.9,;44.85,-28.05,;47.1,-26.52,;46.18,-25.27,;44.66,-25.37,;46.88,-23.89,;48.41,-23.75,;45.97,-22.6,;46.65,-21.19,;48.2,-21.08,;45.79,-19.94,;44.22,-20.08,;43.56,-21.45,;42.02,-21.57,;41.15,-20.3,;41.38,-22.93,;46.44,-18.58,;45.53,-17.27,;44.01,-17.37,;46.23,-15.88,;45.34,-14.62,;46.02,-13.23,;47.54,-13.1,;45.15,-11.97,;43.61,-12.08,;42.91,-13.45,;41.38,-13.59,;40.52,-12.3,;40.73,-14.97,;45.81,-10.56,;44.94,-9.3,;43.4,-9.41,;45.62,-7.92,;47.14,-7.76,;47.99,-9.02,;47.37,-10.45,;49.57,-8.92,;44.71,-6.63,;45.37,-5.25,;46.93,-5.14,;44.5,-3.99,;43,-4.11,;42.31,-5.49,;43.19,-6.74,;42.53,-8.16,;40.99,-8.27,;40.3,-9.63,;40.07,-6.99,;40.77,-5.6,;45.15,-2.58,;44.28,-1.32,;43.19,-2.21,;44.97,.09,;46.51,.19,;47.37,-1.06,;44.05,1.35,;42.74,.58,;42.74,-.96,;41.38,1.35,;41.38,2.88,;42.74,3.65,;40.07,.58,;38.72,1.35,;38.72,2.88,;37.4,.58,;36.05,1.35,;34.73,.58,;34.73,-.96,;33.4,1.35,;33.4,2.88,;34.73,3.65,;36.05,2.88,;34.73,5.21,;32.06,.58,;30.7,1.35,;30.7,2.88,;29.39,.58,;29.39,-.96,;30.7,-1.72,;28.01,1.35,;26.72,.58,;26.72,-.96,;25.34,1.35,;24.03,.58,;22.71,1.35,;22.71,2.88,;21.34,.58,;21.34,-.96,;22.71,-1.72,;24.03,-.96,;25.34,-1.72,;25.34,-3.24,;24.03,-4.06,;22.71,-3.24,;20.04,1.35,;18.69,.58,;18.69,-.96,;17.34,1.35,;16,.58,;14.66,1.35,;14.66,2.88,;13.31,.58,;11.99,1.35,;10.66,.58,;10.66,-.96,;9.3,1.35,;9.3,2.88,;10.66,3.65,;10.66,5.21,;9.3,5.97,;11.99,5.97,;7.98,.58,;6.63,1.35,;6.63,2.88,;5.32,.58,;5.32,-.96,;3.97,1.35,;2.61,.58,;2.61,-.96,;1.3,1.35,;-.02,.58,;1.3,2.88,;2.61,3.65,;4.03,3.04,;5.09,4.18,;4.29,5.54,;2.79,5.21,;17.34,2.88,;16,3.65,;18.69,3.65,;25.34,2.88,;24.03,3.65,;26.72,3.65,;37.4,-.96,;36.05,-1.72,;38.72,-1.72,;39.51,-41.81,;39.42,-43.34,;38.22,-40.98,;36.86,-41.69,;36.79,-43.21,;35.55,-40.81,;35.64,-39.3,;34.19,-41.52,;32.88,-40.66,;32.98,-39.14,;31.68,-38.27,;30.24,-38.81,;29.25,-37.61,;30.14,-36.35,;29.72,-34.87,;30.8,-33.77,;32.32,-34.17,;32.71,-35.65,;31.62,-36.77,;31.52,-41.36,;31.41,-42.91,;30.21,-40.54,;28.83,-41.24,;28.76,-42.74,;27.37,-43.45,;27.31,-44.97,;26.09,-42.6,;27.52,-40.38,;27.62,-38.81,;26.16,-41.08,;24.85,-40.23,;24.97,-38.71,;23.66,-37.83,;26.33,-37.99,;23.49,-40.94,;23.42,-42.46,;22.22,-40.07,;20.82,-40.78,;20.71,-42.3,;19.35,-43.02,;19.28,-44.54,;17.91,-45.25,;17.83,-46.77,;19.51,-39.93,;19.62,-38.38,;18.15,-40.65,;16.87,-39.79,;15.48,-40.49,;15.41,-42.03,;14.17,-39.63,;12.81,-40.33,;12.72,-41.87,;11.36,-42.58,;11.27,-44.1,;9.89,-44.8,;9.8,-46.34,;8.44,-47.05,;11.1,-47.16,;11.5,-39.5,;11.6,-37.94,;10.17,-40.21,;8.86,-39.35,;7.45,-40.07,;6.14,-39.2,;7.38,-41.57,)|
Show InChI InChI=1S/C151H228N40O47/c1-17-77(10)121(148(236)169-81(14)127(215)177-105(60-87-63-160-92-36-25-24-35-90(87)92)138(226)179-101(56-74(4)5)139(227)188-119(75(6)7)146(234)176-94(37-26-28-52-152)130(218)161-65-111(199)170-93(39-30-54-159-151(156)157)129(217)164-68-118(210)211)190-140(228)103(57-84-31-20-18-21-32-84)180-135(223)99(47-51-116(206)207)175-134(222)95(38-27-29-53-153)172-125(213)79(12)166-124(212)78(11)168-133(221)98(44-48-110(155)198)171-112(200)66-162-132(220)97(46-50-115(204)205)174-136(224)100(55-73(2)3)178-137(225)102(59-86-40-42-89(197)43-41-86)181-143(231)107(69-192)184-145(233)109(71-194)185-147(235)120(76(8)9)189-142(230)106(62-117(208)209)182-144(232)108(70-193)186-150(238)123(83(16)196)191-141(229)104(58-85-33-22-19-23-34-85)183-149(237)122(82(15)195)187-113(201)67-163-131(219)96(45-49-114(202)203)173-126(214)80(13)167-128(216)91(154)61-88-64-158-72-165-88/h18-25,31-36,40-43,63-64,72-83,91,93-109,119-123,160,192-197H,17,26-30,37-39,44-62,65-71,152-154H2,1-16H3,(H2,155,198)(H,158,165)(H,161,218)(H,162,220)(H,163,219)(H,164,217)(H,166,212)(H,167,216)(H,168,221)(H,169,236)(H,170,199)(H,171,200)(H,172,213)(H,173,214)(H,174,224)(H,175,222)(H,176,234)(H,177,215)(H,178,225)(H,179,226)(H,180,223)(H,181,231)(H,182,232)(H,183,237)(H,184,233)(H,185,235)(H,186,238)(H,187,201)(H,188,227)(H,189,230)(H,190,228)(H,191,229)(H,202,203)(H,204,205)(H,206,207)(H,208,209)(H,210,211)(H4,156,157,159)/t77-,78-,79-,80-,81-,82+,83+,91-,93-,94-,95-,96-,97-,98-,99-,100-,101-,102-,103-,104-,105-,106-,107-,108-,109-,119-,120-,121-,122-,123-/m0/s1
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
MMDB
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 0.0700n/an/an/an/a



China Pharmaceutical University

Curated by ChEMBL


Assay Description
Agonist activity at full length human GLP1R expressed in HEK293 cells assessed as increase in cAMP accumulation after 20 mins by HTRF assay


Eur J Med Chem 138: 1158-1169 (2017)


Article DOI: 10.1016/j.ejmech.2017.07.046
BindingDB Entry DOI: 10.7270/Q2QC061V
More data for this
Ligand-Target Pair
Glucagon receptor


(Homo sapiens (Human))
BDBM50277081
PNG
(CHEMBL4162383)
Show SMILES CCCCCCN1C(=O)CC(SC[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)Cc2cnc[nH]2)[C@@H](C)O)[C@@H](C)O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](Cc2ccccc2)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](Cc2c[nH]c3ccccc23)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(N)=O)C1=O |r|
Show InChI InChI=1S/C160H234N42O50S2/c1-13-14-15-26-53-202-123(217)67-117(159(202)252)254-75-116(155(248)178-96(35-27-52-171-160(168)169)135(228)175-80(8)132(225)176-98(45-48-119(164)213)137(230)189-109(64-124(218)219)145(238)186-105(57-84-28-18-16-19-29-84)148(241)199-127(79(6)7)156(249)181-99(46-49-120(165)214)138(231)187-107(61-88-68-172-94-33-23-22-32-92(88)94)144(237)183-101(55-77(2)3)140(233)180-100(50-54-253-12)139(232)188-108(63-121(166)215)150(243)200-128(81(9)207)131(167)224)197-154(247)114(73-205)195-147(240)111(66-126(222)223)190-141(234)102(56-78(4)5)182-142(235)103(59-86-36-40-90(210)41-37-86)184-136(229)95(34-24-25-51-161)177-152(245)113(72-204)194-143(236)104(60-87-38-42-91(211)43-39-87)185-146(239)110(65-125(220)221)191-153(246)115(74-206)196-158(251)130(83(11)209)201-149(242)106(58-85-30-20-17-21-31-85)192-157(250)129(82(10)208)198-122(216)70-173-134(227)97(44-47-118(163)212)179-151(244)112(71-203)193-133(226)93(162)62-89-69-170-76-174-89/h16-23,28-33,36-43,68-69,76-83,93,95-117,127-130,172,203-211H,13-15,24-27,34-35,44-67,70-75,161-162H2,1-12H3,(H2,163,212)(H2,164,213)(H2,165,214)(H2,166,215)(H2,167,224)(H,170,174)(H,173,227)(H,175,228)(H,176,225)(H,177,245)(H,178,248)(H,179,244)(H,180,233)(H,181,249)(H,182,235)(H,183,237)(H,184,229)(H,185,239)(H,186,238)(H,187,231)(H,188,232)(H,189,230)(H,190,234)(H,191,246)(H,192,250)(H,193,226)(H,194,236)(H,195,240)(H,196,251)(H,197,247)(H,198,216)(H,199,241)(H,200,243)(H,201,242)(H,218,219)(H,220,221)(H,222,223)(H4,168,169,171)/t80-,81+,82+,83+,93-,95-,96-,97-,98-,99-,100-,101-,102-,103-,104-,105-,106-,107-,108-,109-,110-,111-,112-,113-,114-,115-,116-,117?,127-,128-,129-,130-/m0/s1
PDB
MMDB

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 1.30n/an/an/an/a



China Pharmaceutical University

Curated by ChEMBL


Assay Description
Agonist activity at human GCGR expressed in HEK293 cells assessed as increase in cAMP accumulation after 20 mins by HTRF assay


Eur J Med Chem 138: 1158-1169 (2017)


Article DOI: 10.1016/j.ejmech.2017.07.046
BindingDB Entry DOI: 10.7270/Q2QC061V
More data for this
Ligand-Target Pair
Glucagon receptor


(Homo sapiens (Human))
BDBM50277060
PNG
(CHEMBL4167331)
Show SMILES CSCC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CS)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CO)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)Cc1cnc[nH]1)[C@@H](C)O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(N)=O |r|
Show InChI InChI=1S/C152H226N44O46S2/c1-72(2)52-97(133(225)176-96(47-51-244-11)132(224)184-104(60-115(158)209)142(234)195-120(76(8)201)123(159)215)179-137(229)103(58-83-63-167-89-29-19-18-28-87(83)89)183-130(222)95(43-46-114(157)208)177-148(240)119(74(5)6)194-140(232)101(54-79-24-14-12-15-25-79)182-147(239)111(70-243)192-131(223)94(42-45-113(156)207)171-124(216)75(7)170-127(219)91(31-22-49-165-151(160)161)172-128(220)92(32-23-50-166-152(162)163)174-145(237)109(68-199)190-139(231)106(62-118(213)214)185-134(226)98(53-73(3)4)178-135(227)99(56-81-33-37-85(204)38-34-81)180-129(221)90(30-20-21-48-153)173-144(236)108(67-198)189-136(228)100(57-82-35-39-86(205)40-36-82)181-138(230)105(61-117(211)212)186-146(238)110(69-200)191-150(242)122(78(10)203)196-141(233)102(55-80-26-16-13-17-27-80)187-149(241)121(77(9)202)193-116(210)65-168-126(218)93(41-44-112(155)206)175-143(235)107(66-197)188-125(217)88(154)59-84-64-164-71-169-84/h12-19,24-29,33-40,63-64,71-78,88,90-111,119-122,167,197-205,243H,20-23,30-32,41-62,65-70,153-154H2,1-11H3,(H2,155,206)(H2,156,207)(H2,157,208)(H2,158,209)(H2,159,215)(H,164,169)(H,168,218)(H,170,219)(H,171,216)(H,172,220)(H,173,236)(H,174,237)(H,175,235)(H,176,225)(H,177,240)(H,178,227)(H,179,229)(H,180,221)(H,181,230)(H,182,239)(H,183,222)(H,184,224)(H,185,226)(H,186,238)(H,187,241)(H,188,217)(H,189,228)(H,190,231)(H,191,242)(H,192,223)(H,193,210)(H,194,232)(H,195,234)(H,196,233)(H,211,212)(H,213,214)(H4,160,161,165)(H4,162,163,166)/t75-,76+,77+,78+,88-,90-,91-,92-,93-,94-,95-,96-,97-,98-,99-,100-,101-,102-,103-,104-,105-,106-,107-,108-,109-,110-,111-,119-,120-,121-,122-/m0/s1
PDB
MMDB

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
KEGG
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 1.30n/an/an/an/a



China Pharmaceutical University

Curated by ChEMBL


Assay Description
Agonist activity at human GCGR expressed in HEK293 cells assessed as increase in cAMP accumulation after 20 mins by HTRF assay


Eur J Med Chem 138: 1158-1169 (2017)


Article DOI: 10.1016/j.ejmech.2017.07.046
BindingDB Entry DOI: 10.7270/Q2QC061V
More data for this
Ligand-Target Pair
Glucagon receptor


(Homo sapiens (Human))
BDBM50277053
PNG
(CHEMBL4174382)
Show SMILES CSCC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CO)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CS)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)Cc1cnc[nH]1)[C@@H](C)O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(N)=O |r|
Show InChI InChI=1S/C150H220N44O48S2/c1-70(2)50-94(131(225)174-93(45-49-244-9)130(224)181-100(57-112(156)207)140(234)193-118(73(6)199)121(157)215)176-134(228)99(55-80-61-165-86-27-17-16-26-84(80)86)180-129(223)92(41-44-111(155)206)175-146(240)117(71(3)4)192-138(232)97(51-76-22-12-10-13-23-76)179-135(229)101(58-114(209)210)182-128(222)91(40-43-110(154)205)169-122(216)72(5)168-125(219)88(29-20-47-163-149(158)159)170-126(220)89(30-21-48-164-150(160)161)172-143(237)106(66-197)188-137(231)103(60-116(213)214)184-145(239)108(68-243)190-133(227)96(54-79-33-37-83(203)38-34-79)177-127(221)87(28-18-19-46-151)171-142(236)105(65-196)187-132(226)95(53-78-31-35-82(202)36-32-78)178-136(230)102(59-115(211)212)183-144(238)107(67-198)189-148(242)120(75(8)201)194-139(233)98(52-77-24-14-11-15-25-77)185-147(241)119(74(7)200)191-113(208)63-166-124(218)90(39-42-109(153)204)173-141(235)104(64-195)186-123(217)85(152)56-81-62-162-69-167-81/h10-17,22-27,31-38,61-62,69-75,85,87-108,117-120,165,195-203,243H,18-21,28-30,39-60,63-68,151-152H2,1-9H3,(H2,153,204)(H2,154,205)(H2,155,206)(H2,156,207)(H2,157,215)(H,162,167)(H,166,218)(H,168,219)(H,169,216)(H,170,220)(H,171,236)(H,172,237)(H,173,235)(H,174,225)(H,175,240)(H,176,228)(H,177,221)(H,178,230)(H,179,229)(H,180,223)(H,181,224)(H,182,222)(H,183,238)(H,184,239)(H,185,241)(H,186,217)(H,187,226)(H,188,231)(H,189,242)(H,190,227)(H,191,208)(H,192,232)(H,193,234)(H,194,233)(H,209,210)(H,211,212)(H,213,214)(H4,158,159,163)(H4,160,161,164)/t72-,73+,74+,75+,85-,87-,88-,89-,90-,91-,92-,93-,94-,95-,96-,97-,98-,99-,100-,101-,102-,103-,104-,105-,106-,107-,108-,117-,118-,119-,120-/m0/s1
PDB
MMDB

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
KEGG
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 3.90n/an/an/an/a



China Pharmaceutical University

Curated by ChEMBL


Assay Description
Agonist activity at human GCGR expressed in HEK293 cells assessed as increase in cAMP accumulation after 20 mins by HTRF assay


Eur J Med Chem 138: 1158-1169 (2017)


Article DOI: 10.1016/j.ejmech.2017.07.046
BindingDB Entry DOI: 10.7270/Q2QC061V
More data for this
Ligand-Target Pair
Glucagon-like peptide 1 receptor


(Homo sapiens (Human))
BDBM50277072
PNG
(CHEMBL4174404)
Show SMILES CCCCCCN1C(=O)CC(SC[C@H](NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CO)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)Cc2cnc[nH]2)[C@@H](C)O)[C@@H](C)O)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](Cc2ccccc2)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](Cc2c[nH]c3ccccc23)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(N)=O)C1=O |r|
Show InChI InChI=1S/C163H241N45O50S2/c1-12-13-14-25-55-208-125(223)69-119(161(208)258)260-77-118(157(254)185-100(46-49-121(167)219)139(236)195-111(66-126(224)225)147(244)192-107(59-85-28-17-15-18-29-85)150(247)205-129(81(6)7)158(255)187-101(47-50-122(168)220)140(237)193-109(63-89-70-178-95-33-22-21-32-93(89)95)146(243)189-103(57-79(2)3)142(239)186-102(51-56-259-11)141(238)194-110(65-123(169)221)152(249)206-130(82(8)213)133(170)230)203-138(235)98(36-27-54-177-163(173)174)181-136(233)97(35-26-53-176-162(171)172)183-155(252)116(75-211)201-149(246)113(68-128(228)229)196-143(240)104(58-80(4)5)188-144(241)105(61-87-37-41-91(216)42-38-87)190-137(234)96(34-23-24-52-164)182-154(251)115(74-210)200-145(242)106(62-88-39-43-92(217)44-40-88)191-148(245)112(67-127(226)227)197-156(253)117(76-212)202-160(257)132(84(10)215)207-151(248)108(60-86-30-19-16-20-31-86)198-159(256)131(83(9)214)204-124(222)72-179-135(232)99(45-48-120(166)218)184-153(250)114(73-209)199-134(231)94(165)64-90-71-175-78-180-90/h15-22,28-33,37-44,70-71,78-84,94,96-119,129-132,178,209-217H,12-14,23-27,34-36,45-69,72-77,164-165H2,1-11H3,(H2,166,218)(H2,167,219)(H2,168,220)(H2,169,221)(H2,170,230)(H,175,180)(H,179,232)(H,181,233)(H,182,251)(H,183,252)(H,184,250)(H,185,254)(H,186,239)(H,187,255)(H,188,241)(H,189,243)(H,190,234)(H,191,245)(H,192,244)(H,193,237)(H,194,238)(H,195,236)(H,196,240)(H,197,253)(H,198,256)(H,199,231)(H,200,242)(H,201,246)(H,202,257)(H,203,235)(H,204,222)(H,205,247)(H,206,249)(H,207,248)(H,224,225)(H,226,227)(H,228,229)(H4,171,172,176)(H4,173,174,177)/t82-,83-,84-,94+,96+,97+,98+,99+,100+,101+,102+,103+,104+,105+,106+,107+,108+,109+,110+,111+,112+,113+,114+,115+,116+,117+,118+,119?,129+,130+,131+,132+/m1/s1
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 9n/an/an/an/a



China Pharmaceutical University

Curated by ChEMBL


Assay Description
Agonist activity at full length human GLP1R expressed in HEK293 cells assessed as increase in cAMP accumulation after 20 mins by HTRF assay


Eur J Med Chem 138: 1158-1169 (2017)


Article DOI: 10.1016/j.ejmech.2017.07.046
BindingDB Entry DOI: 10.7270/Q2QC061V
More data for this
Ligand-Target Pair
Glucagon receptor


(Homo sapiens (Human))
BDBM50277054
PNG
(CHEMBL4159275)
Show SMILES CCCCCCCCCCCCCCCCN1C(=O)CC(SC[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)Cc2cnc[nH]2)[C@@H](C)O)[C@@H](C)O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](Cc2ccccc2)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](Cc2c[nH]c3ccccc23)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(N)=O)C1=O |r|
Show InChI InChI=1S/C170H254N42O50S2/c1-13-14-15-16-17-18-19-20-21-22-23-24-25-36-63-212-133(227)77-127(169(212)262)264-85-126(165(258)188-106(45-37-62-181-170(178)179)145(238)185-90(8)142(235)186-108(55-58-129(174)223)147(240)199-119(74-134(228)229)155(248)196-115(67-94-38-28-26-29-39-94)158(251)209-137(89(6)7)166(259)191-109(56-59-130(175)224)148(241)197-117(71-98-78-182-104-43-33-32-42-102(98)104)154(247)193-111(65-87(2)3)150(243)190-110(60-64-263-12)149(242)198-118(73-131(176)225)160(253)210-138(91(9)217)141(177)234)207-164(257)124(83-215)205-157(250)121(76-136(232)233)200-151(244)112(66-88(4)5)192-152(245)113(69-96-46-50-100(220)51-47-96)194-146(239)105(44-34-35-61-171)187-162(255)123(82-214)204-153(246)114(70-97-48-52-101(221)53-49-97)195-156(249)120(75-135(230)231)201-163(256)125(84-216)206-168(261)140(93(11)219)211-159(252)116(68-95-40-30-27-31-41-95)202-167(260)139(92(10)218)208-132(226)80-183-144(237)107(54-57-128(173)222)189-161(254)122(81-213)203-143(236)103(172)72-99-79-180-86-184-99/h26-33,38-43,46-53,78-79,86-93,103,105-127,137-140,182,213-221H,13-25,34-37,44-45,54-77,80-85,171-172H2,1-12H3,(H2,173,222)(H2,174,223)(H2,175,224)(H2,176,225)(H2,177,234)(H,180,184)(H,183,237)(H,185,238)(H,186,235)(H,187,255)(H,188,258)(H,189,254)(H,190,243)(H,191,259)(H,192,245)(H,193,247)(H,194,239)(H,195,249)(H,196,248)(H,197,241)(H,198,242)(H,199,240)(H,200,244)(H,201,256)(H,202,260)(H,203,236)(H,204,246)(H,205,250)(H,206,261)(H,207,257)(H,208,226)(H,209,251)(H,210,253)(H,211,252)(H,228,229)(H,230,231)(H,232,233)(H4,178,179,181)/t90-,91+,92+,93+,103-,105-,106-,107-,108-,109-,110-,111-,112-,113-,114-,115-,116-,117-,118-,119-,120-,121-,122-,123-,124-,125-,126-,127?,137-,138-,139-,140-/m0/s1
PDB
MMDB

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 15n/an/an/an/a



China Pharmaceutical University

Curated by ChEMBL


Assay Description
Agonist activity at human GCGR expressed in HEK293 cells assessed as increase in cAMP accumulation after 20 mins by HTRF assay


Eur J Med Chem 138: 1158-1169 (2017)


Article DOI: 10.1016/j.ejmech.2017.07.046
BindingDB Entry DOI: 10.7270/Q2QC061V
More data for this
Ligand-Target Pair
Glucagon receptor


(Homo sapiens (Human))
BDBM50277082
PNG
(CHEMBL4159003)
Show SMILES CCCCCCCCCCCCCCCCN1C(=O)CC(SC[C@H](NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)Cc2cnc[nH]2)[C@@H](C)O)[C@@H](C)O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](Cc2ccccc2)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](Cc2c[nH]c3ccccc23)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(N)=O)C1=O |r|
Show InChI InChI=1S/C173H261N45O49S2/c1-13-14-15-16-17-18-19-20-21-22-23-24-25-36-66-218-135(232)80-129(171(218)267)269-87-128(167(263)195-109(47-38-65-187-173(183)184)148(244)193-108(46-37-64-186-172(181)182)147(243)191-92(8)144(240)192-111(57-60-131(177)228)150(246)206-122(77-136(233)234)158(254)203-118(70-96-39-28-26-29-40-96)161(257)215-139(91(6)7)168(264)198-112(58-61-132(178)229)151(247)204-120(74-100-81-188-106-44-33-32-43-104(100)106)157(253)200-114(68-89(2)3)153(249)197-113(62-67-268-12)152(248)205-121(76-133(179)230)163(259)216-140(93(9)222)143(180)239)213-160(256)124(79-138(237)238)207-154(250)115(69-90(4)5)199-155(251)116(72-98-48-52-102(225)53-49-98)201-149(245)107(45-34-35-63-174)194-165(261)126(85-220)211-156(252)117(73-99-50-54-103(226)55-51-99)202-159(255)123(78-137(235)236)208-166(262)127(86-221)212-170(266)142(95(11)224)217-162(258)119(71-97-41-30-27-31-42-97)209-169(265)141(94(10)223)214-134(231)83-189-146(242)110(56-59-130(176)227)196-164(260)125(84-219)210-145(241)105(175)75-101-82-185-88-190-101/h26-33,39-44,48-55,81-82,88-95,105,107-129,139-142,188,219-226H,13-25,34-38,45-47,56-80,83-87,174-175H2,1-12H3,(H2,176,227)(H2,177,228)(H2,178,229)(H2,179,230)(H2,180,239)(H,185,190)(H,189,242)(H,191,243)(H,192,240)(H,193,244)(H,194,261)(H,195,263)(H,196,260)(H,197,249)(H,198,264)(H,199,251)(H,200,253)(H,201,245)(H,202,255)(H,203,254)(H,204,247)(H,205,248)(H,206,246)(H,207,250)(H,208,262)(H,209,265)(H,210,241)(H,211,252)(H,212,266)(H,213,256)(H,214,231)(H,215,257)(H,216,259)(H,217,258)(H,233,234)(H,235,236)(H,237,238)(H4,181,182,186)(H4,183,184,187)/t92-,93+,94+,95+,105-,107-,108-,109-,110-,111-,112-,113-,114-,115-,116-,117-,118-,119-,120-,121-,122-,123-,124-,125-,126-,127-,128-,129?,139-,140-,141-,142-/m0/s1
PDB
MMDB

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 4.5n/an/an/an/a



China Pharmaceutical University

Curated by ChEMBL


Assay Description
Agonist activity at human GCGR expressed in HEK293 cells assessed as increase in cAMP accumulation after 20 mins by HTRF assay


Eur J Med Chem 138: 1158-1169 (2017)


Article DOI: 10.1016/j.ejmech.2017.07.046
BindingDB Entry DOI: 10.7270/Q2QC061V
More data for this
Ligand-Target Pair
Glucagon receptor


(Homo sapiens (Human))
BDBM50277083
PNG
(CHEMBL4159426)
Show SMILES CSCC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CS)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CO)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)Cc1cnc[nH]1)[C@@H](C)O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(N)=O |r|
Show InChI InChI=1S/C151H223N43O47S2/c1-71(2)50-95(131(223)173-94(45-49-243-11)130(222)181-102(58-113(156)206)141(233)193-119(75(8)199)122(157)214)176-135(227)101(56-82-62-165-88-29-19-18-28-86(82)88)180-129(221)93(42-44-112(155)205)174-147(239)118(73(5)6)192-139(231)99(52-78-24-14-12-15-25-78)179-137(229)104(60-116(210)211)184-146(238)110(69-242)190-123(215)74(7)168-126(218)90(31-22-47-163-150(158)159)169-127(219)91(32-23-48-164-151(160)161)171-144(236)108(67-197)188-138(230)105(61-117(212)213)182-132(224)96(51-72(3)4)175-133(225)97(54-80-33-37-84(202)38-34-80)177-128(220)89(30-20-21-46-152)170-143(235)107(66-196)187-134(226)98(55-81-35-39-85(203)40-36-81)178-136(228)103(59-115(208)209)183-145(237)109(68-198)189-149(241)121(77(10)201)194-140(232)100(53-79-26-16-13-17-27-79)185-148(240)120(76(9)200)191-114(207)64-166-125(217)92(41-43-111(154)204)172-142(234)106(65-195)186-124(216)87(153)57-83-63-162-70-167-83/h12-19,24-29,33-40,62-63,70-77,87,89-110,118-121,165,195-203,242H,20-23,30-32,41-61,64-69,152-153H2,1-11H3,(H2,154,204)(H2,155,205)(H2,156,206)(H2,157,214)(H,162,167)(H,166,217)(H,168,218)(H,169,219)(H,170,235)(H,171,236)(H,172,234)(H,173,223)(H,174,239)(H,175,225)(H,176,227)(H,177,220)(H,178,228)(H,179,229)(H,180,221)(H,181,222)(H,182,224)(H,183,237)(H,184,238)(H,185,240)(H,186,216)(H,187,226)(H,188,230)(H,189,241)(H,190,215)(H,191,207)(H,192,231)(H,193,233)(H,194,232)(H,208,209)(H,210,211)(H,212,213)(H4,158,159,163)(H4,160,161,164)/t74-,75+,76+,77+,87-,89-,90-,91-,92-,93-,94-,95-,96-,97-,98-,99-,100-,101-,102-,103-,104-,105-,106-,107-,108-,109-,110-,118-,119-,120-,121-/m0/s1
PDB
MMDB

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
KEGG
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 5.30n/an/an/an/a



China Pharmaceutical University

Curated by ChEMBL


Assay Description
Agonist activity at human GCGR expressed in HEK293 cells assessed as increase in cAMP accumulation after 20 mins by HTRF assay


Eur J Med Chem 138: 1158-1169 (2017)


Article DOI: 10.1016/j.ejmech.2017.07.046
BindingDB Entry DOI: 10.7270/Q2QC061V
More data for this
Ligand-Target Pair
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