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SMILES: Cc1ccc(OCCOc2ccc(C[C@H](Nc3ccccc3C(=O)c3ccccc3)C(O)=O)cc2)cc1

InChI Key: InChIKey=YMOQBVUGVRAWNM-LJAQVGFWSA-N

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50471994   
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
Peroxisome proliferator-activated receptor gamma


(Homo sapiens (Human))		BDBM50471994
PNG
(CHEMBL149782)
Show SMILES Cc1ccc(OCCOc2ccc(C[C@H](Nc3ccccc3C(=O)c3ccccc3)C(O)=O)cc2)cc1
Show InChI InChI=1S/C31H29NO5/c1-22-11-15-25(16-12-22)36-19-20-37-26-17-13-23(14-18-26)21-29(31(34)35)32-28-10-6-5-9-27(28)30(33)24-7-3-2-4-8-24/h2-18,29,32H,19-21H2,1H3,(H,34,35)/t29-/m0/s1
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PC cid
PC sid
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Article
PubMed
 93n/an/an/an/an/an/an/an/a



Glaxo Wellcome Research and Development

Curated by ChEMBL


Assay Description
Inhibition by 50% of in vitro binding to Peroxisome proliferator activated receptor gamma

J Med Chem 41: 5037-54 (1998)


Article DOI: 10.1021/jm980413z
BindingDB Entry DOI: 10.7270/Q2J38W9F
More data for this
Ligand-Target Pair