BDBM50194698 4-methyl-N-(2-methyl-3-(trifluoromethyl)phenyl)-3-(2-(2-(piperidin-1-yl)ethylamino)quinazolin-6-yl)benzamide::CHEMBL384942

SMILES: Cc1ccc(cc1-c1ccc2nc(NCCN3CCCCC3)ncc2c1)C(=O)Nc1cccc(c1C)C(F)(F)F

InChI Key: InChIKey=NSOPDMYYXBLFIE-UHFFFAOYSA-N

Data: 4 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 4 hits for monomerid = 50194698   

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 14 (Homo sapiens (Human))	BDBM50194698 (4-methyl-N-(2-methyl-3-(trifluoromethyl)phenyl)-3-...) Show SMILES Cc1ccc(cc1-c1ccc2nc(NCCN3CCCCC3)ncc2c1)C(=O)Nc1cccc(c1C)C(F)(F)F Show InChI InChI=1S/C31H32F3N5O/c1-20-9-10-23(29(40)37-27-8-6-7-26(21(27)2)31(32,33)34)18-25(20)22-11-12-28-24(17-22)19-36-30(38-28)35-13-16-39-14-4-3-5-15-39/h6-12,17-19H,3-5,13-16H2,1-2H3,(H,37,40)(H,35,36,38)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	9	n/a	n/a	n/a	n/a	n/a	n/a
Amgen, Inc. Curated by ChEMBL					Assay Description Inhibition of p38-alpha by HTRF kinase assay				J Med Chem 49: 5671-86 (2006) Article DOI: 10.1021/jm0605482 BindingDB Entry DOI: 10.7270/Q29G5MFD
					More data for this Ligand-Target Pair
Tyrosine-protein kinase JAK3 (Homo sapiens (Human))	BDBM50194698 (4-methyl-N-(2-methyl-3-(trifluoromethyl)phenyl)-3-...) Show SMILES Cc1ccc(cc1-c1ccc2nc(NCCN3CCCCC3)ncc2c1)C(=O)Nc1cccc(c1C)C(F)(F)F Show InChI InChI=1S/C31H32F3N5O/c1-20-9-10-23(29(40)37-27-8-6-7-26(21(27)2)31(32,33)34)18-25(20)22-11-12-28-24(17-22)19-36-30(38-28)35-13-16-39-14-4-3-5-15-39/h6-12,17-19H,3-5,13-16H2,1-2H3,(H,37,40)(H,35,36,38)	PDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	>2.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
Amgen, Inc. Curated by ChEMBL					Assay Description Inhibition of Jak3 by HTRF kinase assay				J Med Chem 49: 5671-86 (2006) Article DOI: 10.1021/jm0605482 BindingDB Entry DOI: 10.7270/Q29G5MFD
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50194698 (4-methyl-N-(2-methyl-3-(trifluoromethyl)phenyl)-3-...) Show SMILES Cc1ccc(cc1-c1ccc2nc(NCCN3CCCCC3)ncc2c1)C(=O)Nc1cccc(c1C)C(F)(F)F Show InChI InChI=1S/C31H32F3N5O/c1-20-9-10-23(29(40)37-27-8-6-7-26(21(27)2)31(32,33)34)18-25(20)22-11-12-28-24(17-22)19-36-30(38-28)35-13-16-39-14-4-3-5-15-39/h6-12,17-19H,3-5,13-16H2,1-2H3,(H,37,40)(H,35,36,38)	PDB UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	6	n/a	n/a	n/a	n/a	n/a	n/a
Amgen, Inc. Curated by ChEMBL					Assay Description Inhibition of Lck by HTRF kinase assay				J Med Chem 49: 5671-86 (2006) Article DOI: 10.1021/jm0605482 BindingDB Entry DOI: 10.7270/Q29G5MFD
					More data for this Ligand-Target Pair
Vascular endothelial growth factor receptor 2 (Homo sapiens (Human))	BDBM50194698 (4-methyl-N-(2-methyl-3-(trifluoromethyl)phenyl)-3-...) Show SMILES Cc1ccc(cc1-c1ccc2nc(NCCN3CCCCC3)ncc2c1)C(=O)Nc1cccc(c1C)C(F)(F)F Show InChI InChI=1S/C31H32F3N5O/c1-20-9-10-23(29(40)37-27-8-6-7-26(21(27)2)31(32,33)34)18-25(20)22-11-12-28-24(17-22)19-36-30(38-28)35-13-16-39-14-4-3-5-15-39/h6-12,17-19H,3-5,13-16H2,1-2H3,(H,37,40)(H,35,36,38)	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	173	n/a	n/a	n/a	n/a	n/a	n/a
Amgen, Inc. Curated by ChEMBL					Assay Description Inhibition of KDR by HTRF kinase assay				J Med Chem 49: 5671-86 (2006) Article DOI: 10.1021/jm0605482 BindingDB Entry DOI: 10.7270/Q29G5MFD
					More data for this Ligand-Target Pair