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SMILES: OC(=O)[C@H](Cc1ccc(OCCc2cccc(F)c2)cc1)Nc1ccccc1C(=O)c1ccccc1

InChI Key: InChIKey=HBQGDOHABDMEFU-NDEPHWFRSA-N

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Similarity at least:  must be >=0.5
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50472001   
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))		BDBM50472001
PNG
(CHEMBL343260)
Show SMILES OC(=O)[C@H](Cc1ccc(OCCc2cccc(F)c2)cc1)Nc1ccccc1C(=O)c1ccccc1
Show InChI InChI=1S/C30H26FNO4/c31-24-10-6-7-21(19-24)17-18-36-25-15-13-22(14-16-25)20-28(30(34)35)32-27-12-5-4-11-26(27)29(33)23-8-2-1-3-9-23/h1-16,19,28,32H,17-18,20H2,(H,34,35)/t28-/m0/s1
PDB
MMDB

NCI pathway
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KEGG

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PC cid
PC sid
UniChem
Article
PubMed
 112n/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