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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(C)(C)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccncc1)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccncc1)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(O)=O

InChI Key: InChIKey=PKCKLTULFGTCMF-AHHJYCKTSA-N

Find this compound or compounds like it in BindingDB or PDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50534606   
Target/Host
(Institution)		LigandTarget/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		pHTemp
°C
Glucagon receptor


(Homo sapiens (Human))		BDBM50534606
PNG
(CHEMBL4466715)
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(C)(C)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccncc1)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccncc1)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(O)=O |r|
Show InChI InChI=1S/C152H225N45O46S/c1-73(2)54-96(131(224)176-95(45-53-244-13)130(223)184-103(62-113(158)207)140(233)196-121(79(10)203)148(241)242)179-135(228)102(60-84-66-168-88-31-21-20-30-86(84)88)183-129(222)94(37-40-112(157)206)177-145(238)118(75(5)6)194-138(231)100(56-80-26-16-14-17-27-80)182-136(229)104(63-115(209)210)185-128(221)93(36-39-111(156)205)172-122(215)76(7)171-125(218)90(33-24-47-166-150(159)160)173-127(220)91(34-25-48-167-151(161)162)192-149(243)152(11,12)197-144(237)106(65-117(213)214)187-132(225)97(55-74(3)4)178-133(226)98(58-82-41-49-163-50-42-82)180-126(219)89(32-22-23-46-153)174-142(235)108(70-199)190-134(227)99(59-83-43-51-164-52-44-83)181-137(230)105(64-116(211)212)186-143(236)109(71-200)191-147(240)120(78(9)202)195-139(232)101(57-81-28-18-15-19-29-81)188-146(239)119(77(8)201)193-114(208)68-169-124(217)92(35-38-110(155)204)175-141(234)107(69-198)189-123(216)87(154)61-85-67-165-72-170-85/h14-21,26-31,41-44,49-52,66-67,72-79,87,89-109,118-121,168,198-203H,22-25,32-40,45-48,53-65,68-71,153-154H2,1-13H3,(H2,155,204)(H2,156,205)(H2,157,206)(H2,158,207)(H,165,170)(H,169,217)(H,171,218)(H,172,215)(H,173,220)(H,174,235)(H,175,234)(H,176,224)(H,177,238)(H,178,226)(H,179,228)(H,180,219)(H,181,230)(H,182,229)(H,183,222)(H,184,223)(H,185,221)(H,186,236)(H,187,225)(H,188,239)(H,189,216)(H,190,227)(H,191,240)(H,192,243)(H,193,208)(H,194,231)(H,195,232)(H,196,233)(H,197,237)(H,209,210)(H,211,212)(H,213,214)(H,241,242)(H4,159,160,166)(H4,161,162,167)/t76-,77+,78+,79+,87-,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 
PC cid
PC sid
UniChem
Article
PubMed
n/an/an/an/a 31n/an/an/an/a



Indiana University

Curated by ChEMBL


Assay Description
Activation of glucagon receptor (unknown origin) transfected in HEK293 cells coinfected with luciferase reporter gene linked CRE element assessed as ...

J Med Chem 59: 8061-7 (2016)


Article DOI: 10.1021/acs.jmedchem.6b00840
More data for this
Ligand-Target Pair