null

SMILES: C=Cc1c(OCc2ccccc2)ccn(Cc2ccccc2)c1=O

InChI Key: InChIKey=RMIINZSMODUZJS-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50310956   

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
Mitogen-activated protein kinase 9 (Homo sapiens (Human))	BDBM50310956 (1-benzyl-4-(benzyloxy)-3-vinylpyridin-2(1H)-one | ...) Show SMILES C=Cc1c(OCc2ccccc2)ccn(Cc2ccccc2)c1=O Show InChI InChI=1S/C21H19NO2/c1-2-19-20(24-16-18-11-7-4-8-12-18)13-14-22(21(19)23)15-17-9-5-3-6-10-17/h2-14H,1,15-16H2	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	>2.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer Corporation Curated by ChEMBL					Assay Description Inhibition of JNK2				Bioorg Med Chem Lett 19: 5851-6 (2009) Article DOI: 10.1016/j.bmcl.2009.08.082 BindingDB Entry DOI: 10.7270/Q2HM59DG
					More data for this Ligand-Target Pair
Mitogen-activated protein kinase 14 (Homo sapiens (Human))	BDBM50310956 (1-benzyl-4-(benzyloxy)-3-vinylpyridin-2(1H)-one | ...) Show SMILES C=Cc1c(OCc2ccccc2)ccn(Cc2ccccc2)c1=O Show InChI InChI=1S/C21H19NO2/c1-2-19-20(24-16-18-11-7-4-8-12-18)13-14-22(21(19)23)15-17-9-5-3-6-10-17/h2-14H,1,15-16H2	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	7.20E+4	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer Corporation Curated by ChEMBL					Assay Description Inhibition of p38alpha				Bioorg Med Chem Lett 19: 5851-6 (2009) Article DOI: 10.1016/j.bmcl.2009.08.082 BindingDB Entry DOI: 10.7270/Q2HM59DG
					More data for this Ligand-Target Pair