null

SMILES: COc1cc2ncn(-c3ccccc3)c2cc1C(O)=O

InChI Key: InChIKey=KUEFIOPBQNNRCA-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 3951   

Target/Host (Institution)	Ligand	Target/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	pH	Temp °C
Platelet-derived growth factor receptor beta (Homo sapiens (Human))	BDBM3951 (5-Methoxy-1-phenylbenzimidazole-6-carboxylic Acid ...) Show SMILES COc1cc2ncn(-c3ccccc3)c2cc1C(O)=O Show InChI InChI=1S/C15H12N2O3/c1-20-14-8-12-13(7-11(14)15(18)19)17(9-16-12)10-5-3-2-4-6-10/h2-9H,1H3,(H,18,19)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	2.10E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Auckland					Assay Description IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...				J Med Chem 42: 2373-82 (1999) Article DOI: 10.1021/jm980658b BindingDB Entry DOI: 10.7270/Q2W957B2
					More data for this Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src (Homo sapiens (Human))	BDBM3951 (5-Methoxy-1-phenylbenzimidazole-6-carboxylic Acid ...) Show SMILES COc1cc2ncn(-c3ccccc3)c2cc1C(O)=O Show InChI InChI=1S/C15H12N2O3/c1-20-14-8-12-13(7-11(14)15(18)19)17(9-16-12)10-5-3-2-4-6-10/h2-9H,1H3,(H,18,19)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	>5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Auckland					Assay Description IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...				J Med Chem 42: 2373-82 (1999) Article DOI: 10.1021/jm980658b BindingDB Entry DOI: 10.7270/Q2W957B2
					More data for this Ligand-Target Pair
Fibroblast growth factor receptor 1 (Homo sapiens (Human))	BDBM3951 (5-Methoxy-1-phenylbenzimidazole-6-carboxylic Acid ...) Show SMILES COc1cc2ncn(-c3ccccc3)c2cc1C(O)=O Show InChI InChI=1S/C15H12N2O3/c1-20-14-8-12-13(7-11(14)15(18)19)17(9-16-12)10-5-3-2-4-6-10/h2-9H,1H3,(H,18,19)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	>5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Auckland					Assay Description IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...				J Med Chem 42: 2373-82 (1999) Article DOI: 10.1021/jm980658b BindingDB Entry DOI: 10.7270/Q2W957B2
					More data for this Ligand-Target Pair