BindingDB logo
myBDB logout

null

SMILES: CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CSC1CC(=O)N(CCC(=O)Nc2ccc(cc2)C(c2c(O)c3ccccc3oc2=O)c2c(O)c3ccccc3oc2=O)C1=O)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)CNC(=O)[C@@H](N)Cc1cnc[nH]1)[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](CCCNC(N)=N)C(N)=O

InChI Key: InChIKey=GZGCWACRWWMVBD-KGMABLQPSA-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 = 50495419   
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-like peptide 1 receptor


(Homo sapiens (Human))
BDBM50495419
PNG
(CHEMBL3110312)
Show SMILES CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CSC1CC(=O)N(CCC(=O)Nc2ccc(cc2)C(c2c(O)c3ccccc3oc2=O)c2c(O)c3ccccc3oc2=O)C1=O)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)CNC(=O)[C@@H](N)Cc1cnc[nH]1)[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](CCCNC(N)=N)C(N)=O |r|
Show InChI InChI=1S/C177H239N41O54S/c1-16-88(10)143(171(265)194-91(13)150(244)202-118(69-98-73-186-106-39-26-23-36-102(98)106)160(254)204-114(65-85(4)5)161(255)214-141(86(6)7)169(263)201-108(40-29-30-61-178)153(247)188-76-129(227)196-107(148(181)242)41-31-62-185-177(182)183)216-162(256)116(66-94-32-19-17-20-33-94)205-157(251)112(55-59-136(236)237)200-168(262)123(82-273-126-72-133(231)218(174(126)268)63-60-128(226)195-99-48-46-97(47-49-99)138(139-146(240)103-37-24-27-42-124(103)271-175(139)269)140-147(241)104-38-25-28-43-125(104)272-176(140)270)212-151(245)90(12)192-149(243)89(11)193-156(250)111(52-56-127(180)225)198-131(229)77-189-155(249)110(54-58-135(234)235)199-158(252)113(64-84(2)3)203-159(253)115(68-96-44-50-101(224)51-45-96)206-165(259)120(79-219)209-167(261)122(81-221)210-170(264)142(87(8)9)215-164(258)119(71-137(238)239)207-166(260)121(80-220)211-173(267)145(93(15)223)217-163(257)117(67-95-34-21-18-22-35-95)208-172(266)144(92(14)222)213-132(230)78-190-154(248)109(53-57-134(232)233)197-130(228)75-187-152(246)105(179)70-100-74-184-83-191-100/h17-28,32-39,42-51,73-74,83-93,105,107-123,126,138,141-145,186,219-224,240-241H,16,29-31,40-41,52-72,75-82,178-179H2,1-15H3,(H2,180,225)(H2,181,242)(H,184,191)(H,187,246)(H,188,247)(H,189,249)(H,190,248)(H,192,243)(H,193,250)(H,194,265)(H,195,226)(H,196,227)(H,197,228)(H,198,229)(H,199,252)(H,200,262)(H,201,263)(H,202,244)(H,203,253)(H,204,254)(H,205,251)(H,206,259)(H,207,260)(H,208,266)(H,209,261)(H,210,264)(H,211,267)(H,212,245)(H,213,230)(H,214,255)(H,215,258)(H,216,256)(H,217,257)(H,232,233)(H,234,235)(H,236,237)(H,238,239)(H4,182,183,185)/t88-,89-,90-,91-,92+,93+,105-,107-,108-,109-,110-,111-,112-,113-,114-,115-,116-,117-,118-,119-,120-,121-,122-,123-,126?,141-,142-,143-,144-,145-/m0/s1
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/an/an/a 0.00200n/an/an/an/a



China Pharmaceutical University

Curated by ChEMBL


Assay Description
Activation of human GLP-1 receptor overexpressed in HEK293 cells assessed as cAMP accumulation after 20 mins by HTRF assay


J Med Chem 56: 9955-68 (2013)


Article DOI: 10.1021/jm4017448
BindingDB Entry DOI: 10.7270/Q2H41VDR
More data for this
Ligand-Target Pair