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2 similar compounds to monomer 50271662

Wt: 370.3
BDBM50271604
Wt: 425.4
BDBM50271732

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50271604,50271732   
Target
(Institution)
LigandTarget
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


(Rattus norvegicus)
BDBM50271732
PNG
(4-(2-(4-((3-hydroxy-1,4-dioxo-1,4-dihydronaphthale...)
Show SMILES O=C1C(Cc2ccc(OCCOc3ccc(cc3)C#N)cc2)C(=O)c2ccccc2C1=O
Show InChI InChI=1S/C26H19NO5/c27-16-18-7-11-20(12-8-18)32-14-13-31-19-9-5-17(6-10-19)15-23-24(28)21-3-1-2-4-22(21)25(29)26(23)30/h1-12,23H,13-15H2
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

AffyNet 
Article
PubMed
n/an/a 1.90E+3n/an/an/an/an/an/a



National Institute of Pharmaceutical Education and Research

Curated by ChEMBL


Assay Description
Displacement of [3H]rosigliatzone from PPARgamma in rat adipocytes


Bioorg Med Chem Lett 18: 3192-5 (2008)

More data for this
Ligand-Target Pair
Peroxisome proliferator-activated receptor gamma


(Rattus norvegicus)
BDBM50271604
PNG
(2-(4-(benzyloxy)benzyl)-3-hydroxynaphthalene-1,4-d...)
Show SMILES O=C1C(Cc2ccc(OCc3ccccc3)cc2)C(=O)c2ccccc2C1=O
Show InChI InChI=1S/C24H18O4/c25-22-19-8-4-5-9-20(19)23(26)24(27)21(22)14-16-10-12-18(13-11-16)28-15-17-6-2-1-3-7-17/h1-13,21H,14-15H2
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

AffyNet 
Article
PubMed
n/an/a 3.60E+3n/an/an/an/an/an/a



National Institute of Pharmaceutical Education and Research

Curated by ChEMBL


Assay Description
Displacement of [3H]rosigliatzone from PPARgamma in rat adipocytes


Bioorg Med Chem Lett 18: 3192-5 (2008)

More data for this
Ligand-Target Pair