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BDBM6617 2-(1H-indol-2-ylcarbonyl)-1H-indol-5-yl 3-phenoxybenzoate::Bis(1H-2-indolyl)methanone deriv. 75::[2-(1H-2-Indolylcarbonyl)-1H-5-indolyl]-3-phenoxybenzoate

SMILES: O=C(Oc1ccc2[nH]c(cc2c1)C(=O)c1cc2ccccc2[nH]1)c1cccc(Oc2ccccc2)c1

InChI Key: InChIKey=SESFCAKZYAECOF-UHFFFAOYSA-N

Data: 1 IC50

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 6617   
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
Platelet-derived growth factor receptor beta


(Homo sapiens (Human))
BDBM6617
PNG
(2-(1H-indol-2-ylcarbonyl)-1H-indol-5-yl 3-phenoxyb...)
Show SMILES O=C(Oc1ccc2[nH]c(cc2c1)C(=O)c1cc2ccccc2[nH]1)c1cccc(Oc2ccccc2)c1
Show InChI InChI=1S/C30H20N2O4/c33-29(27-17-19-7-4-5-12-25(19)31-27)28-18-21-16-24(13-14-26(21)32-28)36-30(34)20-8-6-11-23(15-20)35-22-9-2-1-3-10-22/h1-18,31-32H
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

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PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a>3.00E+4n/an/an/an/an/a25



University of Regensburg



Assay Description
The cells were stimulated with PDGF (100 ng/mL) for 10 min at room temperature. Then the cell lysates were analyzed by SDS-PAGE and immunoblotting wi...


J Med Chem 45: 1002-18 (2002)


Article DOI: 10.1021/jm010988n
BindingDB Entry DOI: 10.7270/Q2GM85H0
More data for this
Ligand-Target Pair