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SMILES: Cc1ccc(=O)n(CCOc2ccc(C[C@H](Nc3ccccc3C(=O)c3ccccc3)C(O)=O)cc2)n1

InChI Key: InChIKey=HMEJFULZHZIJTL-SANMLTNESA-N

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50471988   
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))		BDBM50471988
PNG
(CHEMBL265551)
Show SMILES Cc1ccc(=O)n(CCOc2ccc(C[C@H](Nc3ccccc3C(=O)c3ccccc3)C(O)=O)cc2)n1
Show InChI InChI=1S/C29H27N3O5/c1-20-11-16-27(33)32(31-20)17-18-37-23-14-12-21(13-15-23)19-26(29(35)36)30-25-10-6-5-9-24(25)28(34)22-7-3-2-4-8-22/h2-16,26,30H,17-19H2,1H3,(H,35,36)/t26-/m0/s1
PDB
MMDB

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KEGG

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PC cid
PC sid
UniChem
Article
PubMed
 132n/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