Found 7 hits for monomerid = 50243929 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 |
Focal adhesion kinase 1/vascular endothelial growth factor receptor 3
(Homo sapiens (Human)) | BDBM50243929
(4-[1-(Isopropoxymethyl)-1H-indol-3-yl]-3-(3,4,5-tr...)Show SMILES COc1cc(cc(OC)c1OC)C1=C(CNC1=O)c1cn(COC(C)C)c2ccccc12 |t:13| Show InChI InChI=1S/C25H28N2O5/c1-15(2)32-14-27-13-19(17-8-6-7-9-20(17)27)18-12-26-25(28)23(18)16-10-21(29-3)24(31-5)22(11-16)30-4/h6-11,13,15H,12,14H2,1-5H3,(H,26,28) | PDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 5.30E+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 | |
Aurora kinase A
(Homo sapiens (Human)) | BDBM50243929
(4-[1-(Isopropoxymethyl)-1H-indol-3-yl]-3-(3,4,5-tr...)Show SMILES COc1cc(cc(OC)c1OC)C1=C(CNC1=O)c1cn(COC(C)C)c2ccccc12 |t:13| Show InChI InChI=1S/C25H28N2O5/c1-15(2)32-14-27-13-19(17-8-6-7-9-20(17)27)18-12-26-25(28)23(18)16-10-21(29-3)24(31-5)22(11-16)30-4/h6-11,13,15H,12,14H2,1-5H3,(H,26,28) | 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 | 3.30E+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 Aurora A |
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 | |
Focal adhesion kinase 1
(Homo sapiens (Human)) | BDBM50243929
(4-[1-(Isopropoxymethyl)-1H-indol-3-yl]-3-(3,4,5-tr...)Show SMILES COc1cc(cc(OC)c1OC)C1=C(CNC1=O)c1cn(COC(C)C)c2ccccc12 |t:13| Show InChI InChI=1S/C25H28N2O5/c1-15(2)32-14-27-13-19(17-8-6-7-9-20(17)27)18-12-26-25(28)23(18)16-10-21(29-3)24(31-5)22(11-16)30-4/h6-11,13,15H,12,14H2,1-5H3,(H,26,28) | 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 | 2.70E+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 FAK |
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 | |
Serine/threonine-protein kinase PLK4
(Homo sapiens (Human)) | BDBM50243929
(4-[1-(Isopropoxymethyl)-1H-indol-3-yl]-3-(3,4,5-tr...)Show SMILES COc1cc(cc(OC)c1OC)C1=C(CNC1=O)c1cn(COC(C)C)c2ccccc12 |t:13| Show InChI InChI=1S/C25H28N2O5/c1-15(2)32-14-27-13-19(17-8-6-7-9-20(17)27)18-12-26-25(28)23(18)16-10-21(29-3)24(31-5)22(11-16)30-4/h6-11,13,15H,12,14H2,1-5H3,(H,26,28) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD 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 SAK |
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)) | BDBM50243929
(4-[1-(Isopropoxymethyl)-1H-indol-3-yl]-3-(3,4,5-tr...)Show SMILES COc1cc(cc(OC)c1OC)C1=C(CNC1=O)c1cn(COC(C)C)c2ccccc12 |t:13| Show InChI InChI=1S/C25H28N2O5/c1-15(2)32-14-27-13-19(17-8-6-7-9-20(17)27)18-12-26-25(28)23(18)16-10-21(29-3)24(31-5)22(11-16)30-4/h6-11,13,15H,12,14H2,1-5H3,(H,26,28) | 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 | 5.20E+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 | |
Angiopoietin-1 receptor
(Homo sapiens (Human)) | BDBM50243929
(4-[1-(Isopropoxymethyl)-1H-indol-3-yl]-3-(3,4,5-tr...)Show SMILES COc1cc(cc(OC)c1OC)C1=C(CNC1=O)c1cn(COC(C)C)c2ccccc12 |t:13| Show InChI InChI=1S/C25H28N2O5/c1-15(2)32-14-27-13-19(17-8-6-7-9-20(17)27)18-12-26-25(28)23(18)16-10-21(29-3)24(31-5)22(11-16)30-4/h6-11,13,15H,12,14H2,1-5H3,(H,26,28) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 1.10E+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)) | BDBM50243929
(4-[1-(Isopropoxymethyl)-1H-indol-3-yl]-3-(3,4,5-tr...)Show SMILES COc1cc(cc(OC)c1OC)C1=C(CNC1=O)c1cn(COC(C)C)c2ccccc12 |t:13| Show InChI InChI=1S/C25H28N2O5/c1-15(2)32-14-27-13-19(17-8-6-7-9-20(17)27)18-12-26-25(28)23(18)16-10-21(29-3)24(31-5)22(11-16)30-4/h6-11,13,15H,12,14H2,1-5H3,(H,26,28) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 2.90E+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 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 | |