Found 8 hits for monomerid = 50243880 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 |
Vascular endothelial growth factor receptor 3
(Homo sapiens (Human)) | BDBM50243880
(3-(3,4,5-Trimethoxyphenyl)-4-(1-{[2-(trimethylsily...)Show SMILES COc1cc(cc(OC)c1OC)C1=C(CNC1=O)c1cn(COCC[Si](C)(C)C)c2ccccc12 |t:13| Show InChI InChI=1S/C27H34N2O5Si/c1-31-23-13-18(14-24(32-2)26(23)33-3)25-20(15-28-27(25)30)21-16-29(17-34-11-12-35(4,5)6)22-10-8-7-9-19(21)22/h7-10,13-14,16H,11-12,15,17H2,1-6H3,(H,28,30) | PDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 5.60E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Eberhard-Karls University
Curated by ChEMBL
| Assay Description Inhibition of human recombinant VEGFR3 |
J Med Chem 51: 3814-24 (2008)
Article DOI: 10.1021/jm8001185 BindingDB Entry DOI: 10.7270/Q2057FQS |
More data for this Ligand-Target Pair | |
Epidermal growth factor receptor
(Homo sapiens (Human)) | BDBM50243880
(3-(3,4,5-Trimethoxyphenyl)-4-(1-{[2-(trimethylsily...)Show SMILES COc1cc(cc(OC)c1OC)C1=C(CNC1=O)c1cn(COCC[Si](C)(C)C)c2ccccc12 |t:13| Show InChI InChI=1S/C27H34N2O5Si/c1-31-23-13-18(14-24(32-2)26(23)33-3)25-20(15-28-27(25)30)21-16-29(17-34-11-12-35(4,5)6)22-10-8-7-9-19(21)22/h7-10,13-14,16H,11-12,15,17H2,1-6H3,(H,28,30) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 2.20E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Eberhard-Karls University
Curated by ChEMBL
| Assay Description Inhibition of human recombinant EGFR |
J Med Chem 51: 3814-24 (2008)
Article DOI: 10.1021/jm8001185 BindingDB Entry DOI: 10.7270/Q2057FQS |
More data for this Ligand-Target Pair | |
Ephrin type-B receptor 4
(Homo sapiens (Human)) | BDBM50243880
(3-(3,4,5-Trimethoxyphenyl)-4-(1-{[2-(trimethylsily...)Show SMILES COc1cc(cc(OC)c1OC)C1=C(CNC1=O)c1cn(COCC[Si](C)(C)C)c2ccccc12 |t:13| Show InChI InChI=1S/C27H34N2O5Si/c1-31-23-13-18(14-24(32-2)26(23)33-3)25-20(15-28-27(25)30)21-16-29(17-34-11-12-35(4,5)6)22-10-8-7-9-19(21)22/h7-10,13-14,16H,11-12,15,17H2,1-6H3,(H,28,30) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 4.40E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Eberhard-Karls University
Curated by ChEMBL
| Assay Description Inhibition of human recombinant EPHB4 |
J Med Chem 51: 3814-24 (2008)
Article DOI: 10.1021/jm8001185 BindingDB Entry DOI: 10.7270/Q2057FQS |
More data for this Ligand-Target Pair | |
Angiopoietin-1 receptor
(Homo sapiens (Human)) | BDBM50243880
(3-(3,4,5-Trimethoxyphenyl)-4-(1-{[2-(trimethylsily...)Show SMILES COc1cc(cc(OC)c1OC)C1=C(CNC1=O)c1cn(COCC[Si](C)(C)C)c2ccccc12 |t:13| Show InChI InChI=1S/C27H34N2O5Si/c1-31-23-13-18(14-24(32-2)26(23)33-3)25-20(15-28-27(25)30)21-16-29(17-34-11-12-35(4,5)6)22-10-8-7-9-19(21)22/h7-10,13-14,16H,11-12,15,17H2,1-6H3,(H,28,30) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 2.60E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Eberhard-Karls University
Curated by ChEMBL
| Assay Description Inhibition of human recombinant TIE2 |
J Med Chem 51: 3814-24 (2008)
Article DOI: 10.1021/jm8001185 BindingDB Entry DOI: 10.7270/Q2057FQS |
More data for this Ligand-Target Pair | |
Proto-oncogene tyrosine-protein kinase Src
(Homo sapiens (Human)) | BDBM50243880
(3-(3,4,5-Trimethoxyphenyl)-4-(1-{[2-(trimethylsily...)Show SMILES COc1cc(cc(OC)c1OC)C1=C(CNC1=O)c1cn(COCC[Si](C)(C)C)c2ccccc12 |t:13| Show InChI InChI=1S/C27H34N2O5Si/c1-31-23-13-18(14-24(32-2)26(23)33-3)25-20(15-28-27(25)30)21-16-29(17-34-11-12-35(4,5)6)22-10-8-7-9-19(21)22/h7-10,13-14,16H,11-12,15,17H2,1-6H3,(H,28,30) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 4.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Eberhard-Karls University
Curated by ChEMBL
| Assay Description Inhibition of human recombinant SRC |
J Med Chem 51: 3814-24 (2008)
Article DOI: 10.1021/jm8001185 BindingDB Entry DOI: 10.7270/Q2057FQS |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50243880
(3-(3,4,5-Trimethoxyphenyl)-4-(1-{[2-(trimethylsily...)Show SMILES COc1cc(cc(OC)c1OC)C1=C(CNC1=O)c1cn(COCC[Si](C)(C)C)c2ccccc12 |t:13| Show InChI InChI=1S/C27H34N2O5Si/c1-31-23-13-18(14-24(32-2)26(23)33-3)25-20(15-28-27(25)30)21-16-29(17-34-11-12-35(4,5)6)22-10-8-7-9-19(21)22/h7-10,13-14,16H,11-12,15,17H2,1-6H3,(H,28,30) | 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 | 3.10E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Eberhard-Karls University
Curated by ChEMBL
| Assay Description Inhibition of human recombinant VEGFR2 |
J Med Chem 51: 3814-24 (2008)
Article DOI: 10.1021/jm8001185 BindingDB Entry DOI: 10.7270/Q2057FQS |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50243880
(3-(3,4,5-Trimethoxyphenyl)-4-(1-{[2-(trimethylsily...)Show SMILES COc1cc(cc(OC)c1OC)C1=C(CNC1=O)c1cn(COCC[Si](C)(C)C)c2ccccc12 |t:13| Show InChI InChI=1S/C27H34N2O5Si/c1-31-23-13-18(14-24(32-2)26(23)33-3)25-20(15-28-27(25)30)21-16-29(17-34-11-12-35(4,5)6)22-10-8-7-9-19(21)22/h7-10,13-14,16H,11-12,15,17H2,1-6H3,(H,28,30) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 3.40E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Eberhard-Karls University
Curated by ChEMBL
| Assay Description Inhibition of human recombinant FLT3 |
J Med Chem 51: 3814-24 (2008)
Article DOI: 10.1021/jm8001185 BindingDB Entry DOI: 10.7270/Q2057FQS |
More data for this Ligand-Target Pair | |
Insulin-like growth factor I receptor
(Homo sapiens (Human)) | BDBM50243880
(3-(3,4,5-Trimethoxyphenyl)-4-(1-{[2-(trimethylsily...)Show SMILES COc1cc(cc(OC)c1OC)C1=C(CNC1=O)c1cn(COCC[Si](C)(C)C)c2ccccc12 |t:13| Show InChI InChI=1S/C27H34N2O5Si/c1-31-23-13-18(14-24(32-2)26(23)33-3)25-20(15-28-27(25)30)21-16-29(17-34-11-12-35(4,5)6)22-10-8-7-9-19(21)22/h7-10,13-14,16H,11-12,15,17H2,1-6H3,(H,28,30) | 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 | 8.70E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Eberhard-Karls University
Curated by ChEMBL
| Assay Description Inhibition of human recombinant IGF1R |
J Med Chem 51: 3814-24 (2008)
Article DOI: 10.1021/jm8001185 BindingDB Entry DOI: 10.7270/Q2057FQS |
More data for this Ligand-Target Pair | |