null

SMILES: COc1cc(ccc1NC(=O)c1cc2ccccc2n1C)-c1csc2c(cnc(N)c12)C(N)=O

InChI Key: InChIKey=ZDVCYYIVZCYZRL-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50202744   

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
Tyrosine-protein kinase HCK (Homo sapiens (Human))	BDBM50202744 (4-amino-3-(3-methoxy-4-(1-methyl-1H-indole-2-carbo...) Show SMILES COc1cc(ccc1NC(=O)c1cc2ccccc2n1C)-c1csc2c(cnc(N)c12)C(N)=O Show InChI InChI=1S/C25H21N5O3S/c1-30-18-6-4-3-5-14(18)9-19(30)25(32)29-17-8-7-13(10-20(17)33-2)16-12-34-22-15(24(27)31)11-28-23(26)21(16)22/h3-12H,1-2H3,(H2,26,28)(H2,27,31)(H,29,32)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.41E+3	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Bioresearch Center Curated by ChEMBL					Assay Description Inhibition of Hck				Bioorg Med Chem Lett 17: 1167-71 (2007) Article DOI: 10.1016/j.bmcl.2006.12.035 BindingDB Entry DOI: 10.7270/Q24Q7TN6
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50202744 (4-amino-3-(3-methoxy-4-(1-methyl-1H-indole-2-carbo...) Show SMILES COc1cc(ccc1NC(=O)c1cc2ccccc2n1C)-c1csc2c(cnc(N)c12)C(N)=O Show InChI InChI=1S/C25H21N5O3S/c1-30-18-6-4-3-5-14(18)9-19(30)25(32)29-17-8-7-13(10-20(17)33-2)16-12-34-22-15(24(27)31)11-28-23(26)21(16)22/h3-12H,1-2H3,(H2,26,28)(H2,27,31)(H,29,32)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	380	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Bioresearch Center Curated by ChEMBL					Assay Description Inhibition of Lck				Bioorg Med Chem Lett 17: 1167-71 (2007) Article DOI: 10.1016/j.bmcl.2006.12.035 BindingDB Entry DOI: 10.7270/Q24Q7TN6
					More data for this Ligand-Target Pair