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SMILES: OCCCCCCN1C(=O)C(CCOc2ccccc2CC(O)=O)Oc2ccccc12

InChI Key: InChIKey=NHWYNBPDGCEJRZ-UHFFFAOYSA-N

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50138092   
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))
BDBM50138092
PNG
((2-{2-[4-(6-Hydroxy-hexyl)-3-oxo-3,4-dihydro-2H-be...)
Show SMILES OCCCCCCN1C(=O)C(CCOc2ccccc2CC(O)=O)Oc2ccccc12
Show InChI InChI=1S/C24H29NO6/c26-15-8-2-1-7-14-25-19-10-4-6-12-21(19)31-22(24(25)29)13-16-30-20-11-5-3-9-18(20)17-23(27)28/h3-6,9-12,22,26H,1-2,7-8,13-17H2,(H,27,28)
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

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DrugBank
antibodypedia
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CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 200n/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