Found 2 hits for monomerid = 50277072 Target/Host (Institution) | Ligand | Target/Host Links | Ligand Links | Trg + Lig Links | Ki nM | ΔG° kcal/mole | IC50 nM | Kd nM | EC50/IC50 nM | koff s-1 | kon M-1s-1 | pH | Temp °C |
Glucagon-like peptide 1 receptor
(Homo sapiens (Human)) | BDBM50277072
![PNG](/data/jpeg/tenK5027/BindingDB_50277072.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 ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 9 | n/a | n/a | n/a | n/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)) | BDBM50277072
![PNG](/data/jpeg/tenK5027/BindingDB_50277072.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 ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 2.80 | n/a | n/a | n/a | n/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 | |