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SMILES: Cc1ccc(Oc2ccc(cc2)N2CCC[C@H]2CC(O)=O)cc1

InChI Key: InChIKey=YGNWANUNGJNBAM-INIZCTEOSA-N

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   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50267018   
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
Free fatty acid receptor 1


(Mus musculus)
BDBM50267018
PNG
(CHEMBL4065518)
Show SMILES Cc1ccc(Oc2ccc(cc2)N2CCC[C@H]2CC(O)=O)cc1 |r|
Show InChI InChI=1S/C19H21NO3/c1-14-4-8-17(9-5-14)23-18-10-6-15(7-11-18)20-12-2-3-16(20)13-19(21)22/h4-11,16H,2-3,12-13H2,1H3,(H,21,22)/t16-/m0/s1
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UniProtKB/SwissProt

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PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a>3.30E+4n/an/an/an/a



Bristol-Myers Squibb

Curated by ChEMBL


Assay Description
Agonist activity at GPR40 in mouse STC1 cells assessed as induction of GLP-1 secretion measured after 1 hr by HTRF assay


J Med Chem 60: 1417-1431 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01559
BindingDB Entry DOI: 10.7270/Q25X2CD5
More data for this
Ligand-Target Pair
Free fatty acid receptor 1


(Homo sapiens (Human))
BDBM50267018
PNG
(CHEMBL4065518)
Show SMILES Cc1ccc(Oc2ccc(cc2)N2CCC[C@H]2CC(O)=O)cc1 |r|
Show InChI InChI=1S/C19H21NO3/c1-14-4-8-17(9-5-14)23-18-10-6-15(7-11-18)20-12-2-3-16(20)13-19(21)22/h4-11,16H,2-3,12-13H2,1H3,(H,21,22)/t16-/m0/s1
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 490n/an/an/an/a



Bristol-Myers Squibb

Curated by ChEMBL


Assay Description
Agonist activity at human GPR40 expressed in CHO-A12 cells assessed as increase in intracellular calcium flux measured for 100 secs by FLIPR assay


J Med Chem 60: 1417-1431 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01559
BindingDB Entry DOI: 10.7270/Q25X2CD5
More data for this
Ligand-Target Pair