BindingDB logo
myBDB logout

null

SMILES: CC(=O)NCCCCCCN1C(=O)C(CCOc2ccccc2CC(O)=O)Oc2ccccc12

InChI Key: InChIKey=ZHWBQEQTXOAPRB-UHFFFAOYSA-N

Find this compound or compounds like it in BindingDB or PDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50138091   
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))		BDBM50138091
PNG
((2-{2-[4-(6-Acetylamino-hexyl)-3-oxo-3,4-dihydro-2...)
Show SMILES CC(=O)NCCCCCCN1C(=O)C(CCOc2ccccc2CC(O)=O)Oc2ccccc12
Show InChI InChI=1S/C26H32N2O6/c1-19(29)27-15-8-2-3-9-16-28-21-11-5-7-13-23(21)34-24(26(28)32)14-17-33-22-12-6-4-10-20(22)18-25(30)31/h4-7,10-13,24H,2-3,8-9,14-18H2,1H3,(H,27,29)(H,30,31)
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/an/an/a>5.00E+3n/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