Compile Data Set for Download or QSAR

Found 7 hits of ic50 for monomerid = 50311908   

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))	BDBM50311908 (4-methyl-3-(1-(6-(3-(4-methylpiperazin-1-yl)propyl...) Show SMILES CN1CCN(CCCNc2cc(ncn2)-n2c(Nc3cc(ccc3C)C(=O)Nc3cccc(C)c3)nc3ccccc23)CC1 Show InChI InChI=1S/C34H39N9O/c1-24-8-6-9-27(20-24)38-33(44)26-13-12-25(2)29(21-26)40-34-39-28-10-4-5-11-30(28)43(34)32-22-31(36-23-37-32)35-14-7-15-42-18-16-41(3)17-19-42/h4-6,8-13,20-23H,7,14-19H2,1-3H3,(H,38,44)(H,39,40)(H,35,36,37)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	19	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 Lck (Homo sapiens (Human))	BDBM50311908 (4-methyl-3-(1-(6-(3-(4-methylpiperazin-1-yl)propyl...) Show SMILES CN1CCN(CCCNc2cc(ncn2)-n2c(Nc3cc(ccc3C)C(=O)Nc3cccc(C)c3)nc3ccccc23)CC1 Show InChI InChI=1S/C34H39N9O/c1-24-8-6-9-27(20-24)38-33(44)26-13-12-25(2)29(21-26)40-34-39-28-10-4-5-11-30(28)43(34)32-22-31(36-23-37-32)35-14-7-15-42-18-16-41(3)17-19-42/h4-6,8-13,20-23H,7,14-19H2,1-3H3,(H,38,44)(H,39,40)(H,35,36,37)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	337	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
Vascular endothelial growth factor receptor 2 (Homo sapiens (Human))	BDBM50311908 (4-methyl-3-(1-(6-(3-(4-methylpiperazin-1-yl)propyl...) Show SMILES CN1CCN(CCCNc2cc(ncn2)-n2c(Nc3cc(ccc3C)C(=O)Nc3cccc(C)c3)nc3ccccc23)CC1 Show InChI InChI=1S/C34H39N9O/c1-24-8-6-9-27(20-24)38-33(44)26-13-12-25(2)29(21-26)40-34-39-28-10-4-5-11-30(28)43(34)32-22-31(36-23-37-32)35-14-7-15-42-18-16-41(3)17-19-42/h4-6,8-13,20-23H,7,14-19H2,1-3H3,(H,38,44)(H,39,40)(H,35,36,37)	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	1.11E+3	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
Tyrosine-protein kinase Lyn (Homo sapiens (Human))	BDBM50311908 (4-methyl-3-(1-(6-(3-(4-methylpiperazin-1-yl)propyl...) Show SMILES CN1CCN(CCCNc2cc(ncn2)-n2c(Nc3cc(ccc3C)C(=O)Nc3cccc(C)c3)nc3ccccc23)CC1 Show InChI InChI=1S/C34H39N9O/c1-24-8-6-9-27(20-24)38-33(44)26-13-12-25(2)29(21-26)40-34-39-28-10-4-5-11-30(28)43(34)32-22-31(36-23-37-32)35-14-7-15-42-18-16-41(3)17-19-42/h4-6,8-13,20-23H,7,14-19H2,1-3H3,(H,38,44)(H,39,40)(H,35,36,37)	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	1.23E+3	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
Proto-oncogene tyrosine-protein kinase Src (Homo sapiens (Human))	BDBM50311908 (4-methyl-3-(1-(6-(3-(4-methylpiperazin-1-yl)propyl...) Show SMILES CN1CCN(CCCNc2cc(ncn2)-n2c(Nc3cc(ccc3C)C(=O)Nc3cccc(C)c3)nc3ccccc23)CC1 Show InChI InChI=1S/C34H39N9O/c1-24-8-6-9-27(20-24)38-33(44)26-13-12-25(2)29(21-26)40-34-39-28-10-4-5-11-30(28)43(34)32-22-31(36-23-37-32)35-14-7-15-42-18-16-41(3)17-19-42/h4-6,8-13,20-23H,7,14-19H2,1-3H3,(H,38,44)(H,39,40)(H,35,36,37)	PDB MMDB 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
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 HCK (Homo sapiens (Human))	BDBM50311908 (4-methyl-3-(1-(6-(3-(4-methylpiperazin-1-yl)propyl...) Show SMILES CN1CCN(CCCNc2cc(ncn2)-n2c(Nc3cc(ccc3C)C(=O)Nc3cccc(C)c3)nc3ccccc23)CC1 Show InChI InChI=1S/C34H39N9O/c1-24-8-6-9-27(20-24)38-33(44)26-13-12-25(2)29(21-26)40-34-39-28-10-4-5-11-30(28)43(34)32-22-31(36-23-37-32)35-14-7-15-42-18-16-41(3)17-19-42/h4-6,8-13,20-23H,7,14-19H2,1-3H3,(H,38,44)(H,39,40)(H,35,36,37)	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	1.88E+3	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
Insulin receptor (Homo sapiens (Human))	BDBM50311908 (4-methyl-3-(1-(6-(3-(4-methylpiperazin-1-yl)propyl...) Show SMILES CN1CCN(CCCNc2cc(ncn2)-n2c(Nc3cc(ccc3C)C(=O)Nc3cccc(C)c3)nc3ccccc23)CC1 Show InChI InChI=1S/C34H39N9O/c1-24-8-6-9-27(20-24)38-33(44)26-13-12-25(2)29(21-26)40-34-39-28-10-4-5-11-30(28)43(34)32-22-31(36-23-37-32)35-14-7-15-42-18-16-41(3)17-19-42/h4-6,8-13,20-23H,7,14-19H2,1-3H3,(H,38,44)(H,39,40)(H,35,36,37)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.19E+3	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