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SMILES: CCCCCCCN1C(=O)C(CCOc2ccccc2CC(O)=O)Oc2ccccc12

InChI Key: InChIKey=FDTNPGNXZBBZIQ-UHFFFAOYSA-N

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50138072   
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))		BDBM50138072
PNG
(CHEMBL176770 | {2-[2-(4-Heptyl-3-oxo-3,4-dihydro-2...)
Show SMILES CCCCCCCN1C(=O)C(CCOc2ccccc2CC(O)=O)Oc2ccccc12
Show InChI InChI=1S/C25H31NO5/c1-2-3-4-5-10-16-26-20-12-7-9-14-22(20)31-23(25(26)29)15-17-30-21-13-8-6-11-19(21)18-24(27)28/h6-9,11-14,23H,2-5,10,15-18H2,1H3,(H,27,28)
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Article
PubMed
n/an/an/an/a 234n/an/an/an/a



Johnson and Johnson Pharmaceutical Research and Development

Curated by ChEMBL


Assay Description
Agonistic activity against PPAR (peroxisome proliferator activated receptor gamma) in Suarus chinesis

J Med Chem 47: 196-209 (2003)


Article DOI: 10.1021/jm0301888
BindingDB Entry DOI: 10.7270/Q29Z9495
More data for this
Ligand-Target Pair