BDBM50311940 CHEMBL1080475::N-(3-(1-(6-aminopyrimidin-4-yl)-1H-benzo[d]imidazol-2-ylamino)-4-methylphenyl)-3-tert-butylisonicotinamide

SMILES: Cc1ccc(NC(=O)c2ccncc2C(C)(C)C)cc1Nc1nc2ccccc2n1-c1cc(N)ncn1

InChI Key: InChIKey=SHMSECDXWNWTEF-UHFFFAOYSA-N

Data: 5 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 5 hits for monomerid = 50311940   

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 Lck (Homo sapiens (Human))	BDBM50311940 (CHEMBL1080475 | N-(3-(1-(6-aminopyrimidin-4-yl)-1H...) Show SMILES Cc1ccc(NC(=O)c2ccncc2C(C)(C)C)cc1Nc1nc2ccccc2n1-c1cc(N)ncn1 Show InChI InChI=1S/C28H28N8O/c1-17-9-10-18(33-26(37)19-11-12-30-15-20(19)28(2,3)4)13-22(17)35-27-34-21-7-5-6-8-23(21)36(27)25-14-24(29)31-16-32-25/h5-16H,1-4H3,(H,33,37)(H,34,35)(H2,29,31,32)	PDB UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	10	n/a	n/a	n/a	n/a	n/a	n/a
Genomics Institute of the Novartis Research Foundation (GNF) Curated by ChEMBL					Assay Description Inhibition of LCK				Bioorg Med Chem Lett 19: 6691-5 (2009) Article DOI: 10.1016/j.bmcl.2009.09.123 BindingDB Entry DOI: 10.7270/Q2Q52PRR
					More data for this Ligand-Target Pair
Tyrosine-protein kinase HCK (Homo sapiens (Human))	BDBM50311940 (CHEMBL1080475 | N-(3-(1-(6-aminopyrimidin-4-yl)-1H...) Show SMILES Cc1ccc(NC(=O)c2ccncc2C(C)(C)C)cc1Nc1nc2ccccc2n1-c1cc(N)ncn1 Show InChI InChI=1S/C28H28N8O/c1-17-9-10-18(33-26(37)19-11-12-30-15-20(19)28(2,3)4)13-22(17)35-27-34-21-7-5-6-8-23(21)36(27)25-14-24(29)31-16-32-25/h5-16H,1-4H3,(H,33,37)(H,34,35)(H2,29,31,32)	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	46	n/a	n/a	n/a	n/a	n/a	n/a
Genomics Institute of the Novartis Research Foundation (GNF) Curated by ChEMBL					Assay Description Inhibition of HCK				Bioorg Med Chem Lett 19: 6691-5 (2009) Article DOI: 10.1016/j.bmcl.2009.09.123 BindingDB Entry DOI: 10.7270/Q2Q52PRR
					More data for this Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src (Homo sapiens (Human))	BDBM50311940 (CHEMBL1080475 | N-(3-(1-(6-aminopyrimidin-4-yl)-1H...) Show SMILES Cc1ccc(NC(=O)c2ccncc2C(C)(C)C)cc1Nc1nc2ccccc2n1-c1cc(N)ncn1 Show InChI InChI=1S/C28H28N8O/c1-17-9-10-18(33-26(37)19-11-12-30-15-20(19)28(2,3)4)13-22(17)35-27-34-21-7-5-6-8-23(21)36(27)25-14-24(29)31-16-32-25/h5-16H,1-4H3,(H,33,37)(H,34,35)(H2,29,31,32)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	56	n/a	n/a	n/a	n/a	n/a	n/a
Genomics Institute of the Novartis Research Foundation (GNF) Curated by ChEMBL					Assay Description Inhibition of Tel-fused SRC expressed in mouse BAF3 cells				Bioorg Med Chem Lett 19: 6691-5 (2009) Article DOI: 10.1016/j.bmcl.2009.09.123 BindingDB Entry DOI: 10.7270/Q2Q52PRR
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lyn (Homo sapiens (Human))	BDBM50311940 (CHEMBL1080475 | N-(3-(1-(6-aminopyrimidin-4-yl)-1H...) Show SMILES Cc1ccc(NC(=O)c2ccncc2C(C)(C)C)cc1Nc1nc2ccccc2n1-c1cc(N)ncn1 Show InChI InChI=1S/C28H28N8O/c1-17-9-10-18(33-26(37)19-11-12-30-15-20(19)28(2,3)4)13-22(17)35-27-34-21-7-5-6-8-23(21)36(27)25-14-24(29)31-16-32-25/h5-16H,1-4H3,(H,33,37)(H,34,35)(H2,29,31,32)	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	7	n/a	n/a	n/a	n/a	n/a	n/a
Genomics Institute of the Novartis Research Foundation (GNF) Curated by ChEMBL					Assay Description Inhibition of Tel-fused LYN expressed in mouse BAF3 cells				Bioorg Med Chem Lett 19: 6691-5 (2009) Article DOI: 10.1016/j.bmcl.2009.09.123 BindingDB Entry DOI: 10.7270/Q2Q52PRR
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50311940 (CHEMBL1080475 | N-(3-(1-(6-aminopyrimidin-4-yl)-1H...) Show SMILES Cc1ccc(NC(=O)c2ccncc2C(C)(C)C)cc1Nc1nc2ccccc2n1-c1cc(N)ncn1 Show InChI InChI=1S/C28H28N8O/c1-17-9-10-18(33-26(37)19-11-12-30-15-20(19)28(2,3)4)13-22(17)35-27-34-21-7-5-6-8-23(21)36(27)25-14-24(29)31-16-32-25/h5-16H,1-4H3,(H,33,37)(H,34,35)(H2,29,31,32)	PDB UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	7	n/a	n/a	n/a	n/a	n/a	n/a
Genomics Institute of the Novartis Research Foundation (GNF) Curated by ChEMBL					Assay Description Inhibition of Tel-fused LCK expressed in mouse BAF3 cells				Bioorg Med Chem Lett 19: 6691-5 (2009) Article DOI: 10.1016/j.bmcl.2009.09.123 BindingDB Entry DOI: 10.7270/Q2Q52PRR
					More data for this Ligand-Target Pair