Compile Data Set for Download or QSAR

Found 7 hits of ic50 for monomerid = 50311897   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kJ/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))	BDBM50311897 (3-(1-(6-aminopyrimidin-4-yl)-1H-benzo[d]imidazol-2...) Show SMILES CC(C)c1cccc(NC(=O)c2ccc(C)c(Nc3nc4ccccc4n3-c3cc(N)ncn3)c2)c1 Show InChI InChI=1S/C28H27N7O/c1-17(2)19-7-6-8-21(13-19)32-27(36)20-12-11-18(3)23(14-20)34-28-33-22-9-4-5-10-24(22)35(28)26-15-25(29)30-16-31-26/h4-17H,1-3H3,(H,32,36)(H,33,34)(H2,29,30,31)	PDB UniProtKB/SwissProt 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
Tyrosine-protein kinase Lyn (Homo sapiens (Human))	BDBM50311897 (3-(1-(6-aminopyrimidin-4-yl)-1H-benzo[d]imidazol-2...) Show SMILES CC(C)c1cccc(NC(=O)c2ccc(C)c(Nc3nc4ccccc4n3-c3cc(N)ncn3)c2)c1 Show InChI InChI=1S/C28H27N7O/c1-17(2)19-7-6-8-21(13-19)32-27(36)20-12-11-18(3)23(14-20)34-28-33-22-9-4-5-10-24(22)35(28)26-15-25(29)30-16-31-26/h4-17H,1-3H3,(H,32,36)(H,33,34)(H2,29,30,31)	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	15	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
Vascular endothelial growth factor receptor 2 (Homo sapiens (Human))	BDBM50311897 (3-(1-(6-aminopyrimidin-4-yl)-1H-benzo[d]imidazol-2...) Show SMILES CC(C)c1cccc(NC(=O)c2ccc(C)c(Nc3nc4ccccc4n3-c3cc(N)ncn3)c2)c1 Show InChI InChI=1S/C28H27N7O/c1-17(2)19-7-6-8-21(13-19)32-27(36)20-12-11-18(3)23(14-20)34-28-33-22-9-4-5-10-24(22)35(28)26-15-25(29)30-16-31-26/h4-17H,1-3H3,(H,32,36)(H,33,34)(H2,29,30,31)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	17	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 KDR 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
Proto-oncogene tyrosine-protein kinase Src (Homo sapiens (Human))	BDBM50311897 (3-(1-(6-aminopyrimidin-4-yl)-1H-benzo[d]imidazol-2...) Show SMILES CC(C)c1cccc(NC(=O)c2ccc(C)c(Nc3nc4ccccc4n3-c3cc(N)ncn3)c2)c1 Show InChI InChI=1S/C28H27N7O/c1-17(2)19-7-6-8-21(13-19)32-27(36)20-12-11-18(3)23(14-20)34-28-33-22-9-4-5-10-24(22)35(28)26-15-25(29)30-16-31-26/h4-17H,1-3H3,(H,32,36)(H,33,34)(H2,29,30,31)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	21	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
Insulin receptor (Homo sapiens (Human))	BDBM50311897 (3-(1-(6-aminopyrimidin-4-yl)-1H-benzo[d]imidazol-2...) Show SMILES CC(C)c1cccc(NC(=O)c2ccc(C)c(Nc3nc4ccccc4n3-c3cc(N)ncn3)c2)c1 Show InChI InChI=1S/C28H27N7O/c1-17(2)19-7-6-8-21(13-19)32-27(36)20-12-11-18(3)23(14-20)34-28-33-22-9-4-5-10-24(22)35(28)26-15-25(29)30-16-31-26/h4-17H,1-3H3,(H,32,36)(H,33,34)(H2,29,30,31)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	29	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 InsR 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))	BDBM50311897 (3-(1-(6-aminopyrimidin-4-yl)-1H-benzo[d]imidazol-2...) Show SMILES CC(C)c1cccc(NC(=O)c2ccc(C)c(Nc3nc4ccccc4n3-c3cc(N)ncn3)c2)c1 Show InChI InChI=1S/C28H27N7O/c1-17(2)19-7-6-8-21(13-19)32-27(36)20-12-11-18(3)23(14-20)34-28-33-22-9-4-5-10-24(22)35(28)26-15-25(29)30-16-31-26/h4-17H,1-3H3,(H,32,36)(H,33,34)(H2,29,30,31)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	30	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))	BDBM50311897 (3-(1-(6-aminopyrimidin-4-yl)-1H-benzo[d]imidazol-2...) Show SMILES CC(C)c1cccc(NC(=O)c2ccc(C)c(Nc3nc4ccccc4n3-c3cc(N)ncn3)c2)c1 Show InChI InChI=1S/C28H27N7O/c1-17(2)19-7-6-8-21(13-19)32-27(36)20-12-11-18(3)23(14-20)34-28-33-22-9-4-5-10-24(22)35(28)26-15-25(29)30-16-31-26/h4-17H,1-3H3,(H,32,36)(H,33,34)(H2,29,30,31)	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	151	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