Found 8 hits for monomerid = 50311920 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 |
Insulin receptor
(Homo sapiens (Human)) | BDBM50311920
(CHEMBL1076432 | N-(3-(1-(6-aminopyrimidin-4-yl)-1H...)Show SMILES CN1CCC(CC1)Oc1cc(cc(c1)C(F)(F)F)C(=O)Nc1ccc(C)c(Nc2nc3ccccc3n2-c2cc(N)ncn2)c1 Show InChI InChI=1S/C32H31F3N8O2/c1-19-7-8-22(16-26(19)41-31-40-25-5-3-4-6-27(25)43(31)29-17-28(36)37-18-38-29)39-30(44)20-13-21(32(33,34)35)15-24(14-20)45-23-9-11-42(2)12-10-23/h3-8,13-18,23H,9-12H2,1-2H3,(H,39,44)(H,40,41)(H2,36,37,38) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 746 | 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 | |
Proto-oncogene tyrosine-protein kinase Src
(Homo sapiens (Human)) | BDBM50311920
(CHEMBL1076432 | N-(3-(1-(6-aminopyrimidin-4-yl)-1H...)Show SMILES CN1CCC(CC1)Oc1cc(cc(c1)C(F)(F)F)C(=O)Nc1ccc(C)c(Nc2nc3ccccc3n2-c2cc(N)ncn2)c1 Show InChI InChI=1S/C32H31F3N8O2/c1-19-7-8-22(16-26(19)41-31-40-25-5-3-4-6-27(25)43(31)29-17-28(36)37-18-38-29)39-30(44)20-13-21(32(33,34)35)15-24(14-20)45-23-9-11-42(2)12-10-23/h3-8,13-18,23H,9-12H2,1-2H3,(H,39,44)(H,40,41)(H2,36,37,38) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 39 | 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 Lck
(Homo sapiens (Human)) | BDBM50311920
(CHEMBL1076432 | N-(3-(1-(6-aminopyrimidin-4-yl)-1H...)Show SMILES CN1CCC(CC1)Oc1cc(cc(c1)C(F)(F)F)C(=O)Nc1ccc(C)c(Nc2nc3ccccc3n2-c2cc(N)ncn2)c1 Show InChI InChI=1S/C32H31F3N8O2/c1-19-7-8-22(16-26(19)41-31-40-25-5-3-4-6-27(25)43(31)29-17-28(36)37-18-38-29)39-30(44)20-13-21(32(33,34)35)15-24(14-20)45-23-9-11-42(2)12-10-23/h3-8,13-18,23H,9-12H2,1-2H3,(H,39,44)(H,40,41)(H2,36,37,38) | PDB
UniProtKB/SwissProt UniProtKB/TrEMBL
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 24 | 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)) | BDBM50311920
(CHEMBL1076432 | N-(3-(1-(6-aminopyrimidin-4-yl)-1H...)Show SMILES CN1CCC(CC1)Oc1cc(cc(c1)C(F)(F)F)C(=O)Nc1ccc(C)c(Nc2nc3ccccc3n2-c2cc(N)ncn2)c1 Show InChI InChI=1S/C32H31F3N8O2/c1-19-7-8-22(16-26(19)41-31-40-25-5-3-4-6-27(25)43(31)29-17-28(36)37-18-38-29)39-30(44)20-13-21(32(33,34)35)15-24(14-20)45-23-9-11-42(2)12-10-23/h3-8,13-18,23H,9-12H2,1-2H3,(H,39,44)(H,40,41)(H2,36,37,38) | PDB MMDB
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 | 27 | 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 | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50311920
(CHEMBL1076432 | N-(3-(1-(6-aminopyrimidin-4-yl)-1H...)Show SMILES CN1CCC(CC1)Oc1cc(cc(c1)C(F)(F)F)C(=O)Nc1ccc(C)c(Nc2nc3ccccc3n2-c2cc(N)ncn2)c1 Show InChI InChI=1S/C32H31F3N8O2/c1-19-7-8-22(16-26(19)41-31-40-25-5-3-4-6-27(25)43(31)29-17-28(36)37-18-38-29)39-30(44)20-13-21(32(33,34)35)15-24(14-20)45-23-9-11-42(2)12-10-23/h3-8,13-18,23H,9-12H2,1-2H3,(H,39,44)(H,40,41)(H2,36,37,38) | PDB
UniProtKB/SwissProt UniProtKB/TrEMBL
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
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)) | BDBM50311920
(CHEMBL1076432 | N-(3-(1-(6-aminopyrimidin-4-yl)-1H...)Show SMILES CN1CCC(CC1)Oc1cc(cc(c1)C(F)(F)F)C(=O)Nc1ccc(C)c(Nc2nc3ccccc3n2-c2cc(N)ncn2)c1 Show InChI InChI=1S/C32H31F3N8O2/c1-19-7-8-22(16-26(19)41-31-40-25-5-3-4-6-27(25)43(31)29-17-28(36)37-18-38-29)39-30(44)20-13-21(32(33,34)35)15-24(14-20)45-23-9-11-42(2)12-10-23/h3-8,13-18,23H,9-12H2,1-2H3,(H,39,44)(H,40,41)(H2,36,37,38) | PDB MMDB
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 | 5 | 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)) | BDBM50311920
(CHEMBL1076432 | N-(3-(1-(6-aminopyrimidin-4-yl)-1H...)Show SMILES CN1CCC(CC1)Oc1cc(cc(c1)C(F)(F)F)C(=O)Nc1ccc(C)c(Nc2nc3ccccc3n2-c2cc(N)ncn2)c1 Show InChI InChI=1S/C32H31F3N8O2/c1-19-7-8-22(16-26(19)41-31-40-25-5-3-4-6-27(25)43(31)29-17-28(36)37-18-38-29)39-30(44)20-13-21(32(33,34)35)15-24(14-20)45-23-9-11-42(2)12-10-23/h3-8,13-18,23H,9-12H2,1-2H3,(H,39,44)(H,40,41)(H2,36,37,38) | 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 | 66 | 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)) | BDBM50311920
(CHEMBL1076432 | N-(3-(1-(6-aminopyrimidin-4-yl)-1H...)Show SMILES CN1CCC(CC1)Oc1cc(cc(c1)C(F)(F)F)C(=O)Nc1ccc(C)c(Nc2nc3ccccc3n2-c2cc(N)ncn2)c1 Show InChI InChI=1S/C32H31F3N8O2/c1-19-7-8-22(16-26(19)41-31-40-25-5-3-4-6-27(25)43(31)29-17-28(36)37-18-38-29)39-30(44)20-13-21(32(33,34)35)15-24(14-20)45-23-9-11-42(2)12-10-23/h3-8,13-18,23H,9-12H2,1-2H3,(H,39,44)(H,40,41)(H2,36,37,38) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 233 | 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 SRC |
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 | |