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SMILES: CCOC(=O)c1cccc(c1)-n1cnc2ccccc12

InChI Key: InChIKey=MDQZYXFGOFYIJS-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 3813   

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
Fibroblast growth factor receptor 1 (Homo sapiens (Human))	BDBM3813 (1-Phenylbenzimidazole deriv. 30 | ethyl 3-(1H-1,3-...) Show SMILES CCOC(=O)c1cccc(c1)-n1cnc2ccccc12 Show InChI InChI=1S/C16H14N2O2/c1-2-20-16(19)12-6-5-7-13(10-12)18-11-17-14-8-3-4-9-15(14)18/h3-11H,2H2,1H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem 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 41: 5457-65 (1998) Article DOI: 10.1021/jm9804681 BindingDB Entry DOI: 10.7270/Q24T6GJC
					More data for this Ligand-Target Pair
Platelet-derived growth factor receptor beta (Homo sapiens (Human))	BDBM3813 (1-Phenylbenzimidazole deriv. 30 | ethyl 3-(1H-1,3-...) Show SMILES CCOC(=O)c1cccc(c1)-n1cnc2ccccc12 Show InChI InChI=1S/C16H14N2O2/c1-2-20-16(19)12-6-5-7-13(10-12)18-11-17-14-8-3-4-9-15(14)18/h3-11H,2H2,1H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem 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 41: 5457-65 (1998) Article DOI: 10.1021/jm9804681 BindingDB Entry DOI: 10.7270/Q24T6GJC
					More data for this Ligand-Target Pair