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Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'Glucagon-like peptide 1 receptor' and Ligand = 'BDBM50266691'   
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))
BDBM50266691
PNG
(CHEMBL4086979)
Show SMILES CCCCCCCCCCCCCCCC(=O)N[C@@H](CCC(=O)NCCCC[C@H](NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](CC(C)C)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(O)=O)C(=O)N[C@@H](CO)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](Cc1ccccc1)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(N)=O)C(=O)NCC(=O)NCC(=O)N1CCC[C@H]1C(=O)N[C@@H](CO)C(=O)N[C@@H](CO)C(=O)NCC(=O)N[C@@H](C)C(=O)N1CCC[C@H]1C(=O)N1CCC[C@H]1C(=O)N1CCC[C@H]1C(=O)N[C@@H](CO)C(N)=O)C(O)=O |r|
Show InChI InChI=1S/C203H319N57O64/c1-12-14-15-16-17-18-19-20-21-22-23-24-31-61-154(275)228-128(201(323)324)65-70-153(274)217-74-39-36-54-121(230-177(299)126(64-69-151(209)272)236-173(295)119(52-34-37-72-204)233-189(311)141(100-264)250-181(303)130(82-106(5)6)239-183(305)136(89-161(284)285)245-191(313)144(103-267)253-197(319)165(111(11)269)256-187(309)132(84-113-48-29-26-30-49-113)246-196(318)164(110(10)268)254-157(278)95-223-169(291)124(62-67-149(207)270)235-188(310)140(99-263)248-168(290)117(206)86-115-92-216-104-225-115)176(298)243-137(90-162(286)287)185(307)251-142(101-265)190(312)234-123(56-41-76-219-203(214)215)174(296)231-122(55-40-75-218-202(212)213)172(294)227-108(8)167(289)229-125(63-68-150(208)271)178(300)244-135(88-160(282)283)184(306)240-131(83-112-46-27-25-28-47-112)186(308)255-163(107(7)13-2)195(317)237-127(66-71-159(280)281)179(301)241-133(85-114-91-220-118-51-33-32-50-116(114)118)182(304)238-129(81-105(3)4)180(302)232-120(53-35-38-73-205)175(297)242-134(87-152(210)273)170(292)222-93-155(276)221-96-158(279)257-77-42-57-145(257)193(315)252-143(102-266)192(314)249-139(98-262)171(293)224-94-156(277)226-109(9)198(320)259-79-44-59-147(259)200(322)260-80-45-60-148(260)199(321)258-78-43-58-146(258)194(316)247-138(97-261)166(211)288/h25-30,32-33,46-51,91-92,104-111,117,119-148,163-165,220,261-269H,12-24,31,34-45,52-90,93-103,204-206H2,1-11H3,(H2,207,270)(H2,208,271)(H2,209,272)(H2,210,273)(H2,211,288)(H,216,225)(H,217,274)(H,221,276)(H,222,292)(H,223,291)(H,224,293)(H,226,277)(H,227,294)(H,228,275)(H,229,289)(H,230,299)(H,231,296)(H,232,302)(H,233,311)(H,234,312)(H,235,310)(H,236,295)(H,237,317)(H,238,304)(H,239,305)(H,240,306)(H,241,301)(H,242,297)(H,243,298)(H,244,300)(H,245,313)(H,246,318)(H,247,316)(H,248,290)(H,249,314)(H,250,303)(H,251,307)(H,252,315)(H,253,319)(H,254,278)(H,255,308)(H,256,309)(H,280,281)(H,282,283)(H,284,285)(H,286,287)(H,323,324)(H4,212,213,218)(H4,214,215,219)/t107-,108-,109-,110+,111+,117-,119-,120-,121-,122-,123-,124-,125-,126-,127-,128-,129-,130-,131-,132-,133-,134-,135-,136-,137-,138-,139-,140-,141-,142-,143-,144-,145-,146-,147-,148-,163-,164-,165-/m0/s1
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 0.00390n/an/an/an/a



Sanofi-Aventis Deutschland GmbH

Curated by ChEMBL


Assay Description
Agonist activity at human GLP-1 receptor expressed in HEK293 cells assessed as cAMP accumulation after 30 mins by HTRF assay


J Med Chem 60: 4293-4303 (2017)


Article DOI: 10.1021/acs.jmedchem.7b00174
BindingDB Entry DOI: 10.7270/Q27S7R7M
More data for this
Ligand-Target Pair
Glucagon-like peptide 1 receptor


(Mus musculus)
BDBM50266691
PNG
(CHEMBL4086979)
Show SMILES CCCCCCCCCCCCCCCC(=O)N[C@@H](CCC(=O)NCCCC[C@H](NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](CC(C)C)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(O)=O)C(=O)N[C@@H](CO)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](Cc1ccccc1)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(N)=O)C(=O)NCC(=O)NCC(=O)N1CCC[C@H]1C(=O)N[C@@H](CO)C(=O)N[C@@H](CO)C(=O)NCC(=O)N[C@@H](C)C(=O)N1CCC[C@H]1C(=O)N1CCC[C@H]1C(=O)N1CCC[C@H]1C(=O)N[C@@H](CO)C(N)=O)C(O)=O |r|
Show InChI InChI=1S/C203H319N57O64/c1-12-14-15-16-17-18-19-20-21-22-23-24-31-61-154(275)228-128(201(323)324)65-70-153(274)217-74-39-36-54-121(230-177(299)126(64-69-151(209)272)236-173(295)119(52-34-37-72-204)233-189(311)141(100-264)250-181(303)130(82-106(5)6)239-183(305)136(89-161(284)285)245-191(313)144(103-267)253-197(319)165(111(11)269)256-187(309)132(84-113-48-29-26-30-49-113)246-196(318)164(110(10)268)254-157(278)95-223-169(291)124(62-67-149(207)270)235-188(310)140(99-263)248-168(290)117(206)86-115-92-216-104-225-115)176(298)243-137(90-162(286)287)185(307)251-142(101-265)190(312)234-123(56-41-76-219-203(214)215)174(296)231-122(55-40-75-218-202(212)213)172(294)227-108(8)167(289)229-125(63-68-150(208)271)178(300)244-135(88-160(282)283)184(306)240-131(83-112-46-27-25-28-47-112)186(308)255-163(107(7)13-2)195(317)237-127(66-71-159(280)281)179(301)241-133(85-114-91-220-118-51-33-32-50-116(114)118)182(304)238-129(81-105(3)4)180(302)232-120(53-35-38-73-205)175(297)242-134(87-152(210)273)170(292)222-93-155(276)221-96-158(279)257-77-42-57-145(257)193(315)252-143(102-266)192(314)249-139(98-262)171(293)224-94-156(277)226-109(9)198(320)259-79-44-59-147(259)200(322)260-80-45-60-148(260)199(321)258-78-43-58-146(258)194(316)247-138(97-261)166(211)288/h25-30,32-33,46-51,91-92,104-111,117,119-148,163-165,220,261-269H,12-24,31,34-45,52-90,93-103,204-206H2,1-11H3,(H2,207,270)(H2,208,271)(H2,209,272)(H2,210,273)(H2,211,288)(H,216,225)(H,217,274)(H,221,276)(H,222,292)(H,223,291)(H,224,293)(H,226,277)(H,227,294)(H,228,275)(H,229,289)(H,230,299)(H,231,296)(H,232,302)(H,233,311)(H,234,312)(H,235,310)(H,236,295)(H,237,317)(H,238,304)(H,239,305)(H,240,306)(H,241,301)(H,242,297)(H,243,298)(H,244,300)(H,245,313)(H,246,318)(H,247,316)(H,248,290)(H,249,314)(H,250,303)(H,251,307)(H,252,315)(H,253,319)(H,254,278)(H,255,308)(H,256,309)(H,280,281)(H,282,283)(H,284,285)(H,286,287)(H,323,324)(H4,212,213,218)(H4,214,215,219)/t107-,108-,109-,110+,111+,117-,119-,120-,121-,122-,123-,124-,125-,126-,127-,128-,129-,130-,131-,132-,133-,134-,135-,136-,137-,138-,139-,140-,141-,142-,143-,144-,145-,146-,147-,148-,163-,164-,165-/m0/s1
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 0.00230n/an/an/an/a



Sanofi-Aventis Deutschland GmbH

Curated by ChEMBL


Assay Description
Agonist activity at mouse GLP-1 receptor expressed in HEK293 cells assessed as cAMP accumulation after 30 mins by HTRF assay


J Med Chem 60: 4293-4303 (2017)


Article DOI: 10.1021/acs.jmedchem.7b00174
BindingDB Entry DOI: 10.7270/Q27S7R7M
More data for this
Ligand-Target Pair