BDBM15925 Aminopyridine-Based Inhibitor 6d::N-(4-Amino-5-cyano-6-ethoxypyridin-2-yl)-3-methylbutyramide::N-(4-amino-5-cyano-6-ethoxypyridin-2-yl)-3-methylbutanamide

SMILES: CCOc1nc(NC(=O)CC(C)C)cc(N)c1C#N

InChI Key: InChIKey=GRLTUBWHERWKSB-UHFFFAOYSA-N

Data: 2 IC50

Find this compound or compounds like it in BindingDB or PDB:

Substructure Similarity at least:  must be >=0.5 Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 15925   

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))	BDBM15925 (Aminopyridine-Based Inhibitor 6d | N-(4-Amino-5-cy...) Show SMILES CCOc1nc(NC(=O)CC(C)C)cc(N)c1C#N Show InChI InChI=1S/C13H18N4O2/c1-4-19-13-9(7-14)10(15)6-11(17-13)16-12(18)5-8(2)3/h6,8H,4-5H2,1-3H3,(H3,15,16,17,18)	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	3.50E+3	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories					Assay Description In vitro substrate phosphorylation using purified recombinant JNK, was incubated with substrate, and test compounds in the presence of 5uM ATP/ [gamm...				J Med Chem 49: 3563-80 (2006) Article DOI: 10.1021/jm060199b BindingDB Entry DOI: 10.7270/Q2P26WDX
					More data for this Ligand-Target Pair
Mitogen-activated protein kinase 8 (Homo sapiens (Human))	BDBM15925 (Aminopyridine-Based Inhibitor 6d | N-(4-Amino-5-cy...) Show SMILES CCOc1nc(NC(=O)CC(C)C)cc(N)c1C#N Show InChI InChI=1S/C13H18N4O2/c1-4-19-13-9(7-14)10(15)6-11(17-13)16-12(18)5-8(2)3/h6,8H,4-5H2,1-3H3,(H3,15,16,17,18)	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	1.40E+3	n/a	n/a	n/a	n/a	7.2	20
Abbott Laboratories					Assay Description In vitro substrate phosphorylation using purified recombinant JNK, was incubated with substrate, and test compounds in the presence of 5uM ATP/ [gamm...				J Med Chem 49: 3563-80 (2006) Article DOI: 10.1021/jm060199b BindingDB Entry DOI: 10.7270/Q2P26WDX
					More data for this Ligand-Target Pair