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BDBM50511212 CHEMBL4471493

SMILES: OC(=O)c1cccc(NCc2ccc(OCc3ccc(I)cc3)cc2)c1

InChI Key: InChIKey=TWKFJNSYUNFJRF-UHFFFAOYSA-N

Data: 1 EC50

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50511212   
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


(Homo sapiens (Human))		BDBM50511212
PNG
(CHEMBL4471493)
Show SMILES OC(=O)c1cccc(NCc2ccc(OCc3ccc(I)cc3)cc2)c1
Show InChI InChI=1S/C21H18INO3/c22-18-8-4-16(5-9-18)14-26-20-10-6-15(7-11-20)13-23-19-3-1-2-17(12-19)21(24)25/h1-12,23H,13-14H2,(H,24,25)
PDB

UniProtKB/SwissProt
UniProtKB/TrEMBL

antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/an/an/a 1.45E+3n/an/an/an/a



University of Oklahoma

Curated by ChEMBL


Assay Description
Agonist activity at human PPARalpha expressed in nonhuman mammalian cells assessed as increase in receptor transcriptional activity incubated for 22 ...

J Med Chem 63: 2854-2876 (2020)


Article DOI: 10.1021/acs.jmedchem.9b01189
More data for this
Ligand-Target Pair