Found 8 hits for monomerid = 50137576 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 |
Tyrosine-protein kinase Fyn
(Homo sapiens (Human)) | BDBM50137576
(3-[1-{3-[3-(4-Hydroxy-piperidin-1-yl)-propyl]-4,5,...)Show SMILES CNS(=O)(=O)c1ccc2NC(=O)\C(=C/c3[nH]c4CCCCc4c3CCCN3CCC(O)CC3)c2c1 Show InChI InChI=1S/C26H34N4O4S/c1-27-35(33,34)18-8-9-24-21(15-18)22(26(32)29-24)16-25-20(19-5-2-3-7-23(19)28-25)6-4-12-30-13-10-17(31)11-14-30/h8-9,15-17,27-28,31H,2-7,10-14H2,1H3,(H,29,32)/b22-16- | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| PubMed
| n/a | n/a | 200 | n/a | n/a | n/a | n/a | n/a | n/a |
SUGEN, Inc.
Curated by ChEMBL
| Assay Description Inhibitory activity against Fyn tyrosine kinase |
Bioorg Med Chem Lett 14: 187-90 (2003)
BindingDB Entry DOI: 10.7270/Q2HM57VG |
More data for this Ligand-Target Pair | |
Platelet-derived growth factor receptor beta
(Homo sapiens (Human)) | BDBM50137576
(3-[1-{3-[3-(4-Hydroxy-piperidin-1-yl)-propyl]-4,5,...)Show SMILES CNS(=O)(=O)c1ccc2NC(=O)\C(=C/c3[nH]c4CCCCc4c3CCCN3CCC(O)CC3)c2c1 Show InChI InChI=1S/C26H34N4O4S/c1-27-35(33,34)18-8-9-24-21(15-18)22(26(32)29-24)16-25-20(19-5-2-3-7-23(19)28-25)6-4-12-30-13-10-17(31)11-14-30/h8-9,15-17,27-28,31H,2-7,10-14H2,1H3,(H,29,32)/b22-16- | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| PubMed
| n/a | n/a | 4.70E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
SUGEN, Inc.
Curated by ChEMBL
| Assay Description Inhibitory activity against PDGFRbeta tyrosine kinase |
Bioorg Med Chem Lett 14: 187-90 (2003)
BindingDB Entry DOI: 10.7270/Q2HM57VG |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50137576
(3-[1-{3-[3-(4-Hydroxy-piperidin-1-yl)-propyl]-4,5,...)Show SMILES CNS(=O)(=O)c1ccc2NC(=O)\C(=C/c3[nH]c4CCCCc4c3CCCN3CCC(O)CC3)c2c1 Show InChI InChI=1S/C26H34N4O4S/c1-27-35(33,34)18-8-9-24-21(15-18)22(26(32)29-24)16-25-20(19-5-2-3-7-23(19)28-25)6-4-12-30-13-10-17(31)11-14-30/h8-9,15-17,27-28,31H,2-7,10-14H2,1H3,(H,29,32)/b22-16- | PDB
UniProtKB/SwissProt UniProtKB/TrEMBL
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| PubMed
| n/a | n/a | 300 | n/a | n/a | n/a | n/a | n/a | n/a |
SUGEN, Inc.
Curated by ChEMBL
| Assay Description Inhibitory activity against Lck tyrosine kinase |
Bioorg Med Chem Lett 14: 187-90 (2003)
BindingDB Entry DOI: 10.7270/Q2HM57VG |
More data for this Ligand-Target Pair | |
Proto-oncogene tyrosine-protein kinase Src
(Homo sapiens (Human)) | BDBM50137576
(3-[1-{3-[3-(4-Hydroxy-piperidin-1-yl)-propyl]-4,5,...)Show SMILES CNS(=O)(=O)c1ccc2NC(=O)\C(=C/c3[nH]c4CCCCc4c3CCCN3CCC(O)CC3)c2c1 Show InChI InChI=1S/C26H34N4O4S/c1-27-35(33,34)18-8-9-24-21(15-18)22(26(32)29-24)16-25-20(19-5-2-3-7-23(19)28-25)6-4-12-30-13-10-17(31)11-14-30/h8-9,15-17,27-28,31H,2-7,10-14H2,1H3,(H,29,32)/b22-16- | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| PubMed
| n/a | n/a | 50 | n/a | n/a | n/a | n/a | n/a | n/a |
SUGEN, Inc.
Curated by ChEMBL
| Assay Description Inhibitory activity against cellular Src protein tryrosine kinase using the actin ring assay |
Bioorg Med Chem Lett 14: 187-90 (2003)
BindingDB Entry DOI: 10.7270/Q2HM57VG |
More data for this Ligand-Target Pair | |
Fibroblast growth factor receptor 1
(Homo sapiens (Human)) | BDBM50137576
(3-[1-{3-[3-(4-Hydroxy-piperidin-1-yl)-propyl]-4,5,...)Show SMILES CNS(=O)(=O)c1ccc2NC(=O)\C(=C/c3[nH]c4CCCCc4c3CCCN3CCC(O)CC3)c2c1 Show InChI InChI=1S/C26H34N4O4S/c1-27-35(33,34)18-8-9-24-21(15-18)22(26(32)29-24)16-25-20(19-5-2-3-7-23(19)28-25)6-4-12-30-13-10-17(31)11-14-30/h8-9,15-17,27-28,31H,2-7,10-14H2,1H3,(H,29,32)/b22-16- | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| PubMed
| n/a | n/a | 3.40E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
SUGEN, Inc.
Curated by ChEMBL
| Assay Description Inhibitory activity against Fibroblast growth factor receptor 1 |
Bioorg Med Chem Lett 14: 187-90 (2003)
BindingDB Entry DOI: 10.7270/Q2HM57VG |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50137576
(3-[1-{3-[3-(4-Hydroxy-piperidin-1-yl)-propyl]-4,5,...)Show SMILES CNS(=O)(=O)c1ccc2NC(=O)\C(=C/c3[nH]c4CCCCc4c3CCCN3CCC(O)CC3)c2c1 Show InChI InChI=1S/C26H34N4O4S/c1-27-35(33,34)18-8-9-24-21(15-18)22(26(32)29-24)16-25-20(19-5-2-3-7-23(19)28-25)6-4-12-30-13-10-17(31)11-14-30/h8-9,15-17,27-28,31H,2-7,10-14H2,1H3,(H,29,32)/b22-16- | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| PubMed
| n/a | n/a | 7.10E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
SUGEN, Inc.
Curated by ChEMBL
| Assay Description Inhibitory activity against Vascular endothelial growth factor receptor 2 |
Bioorg Med Chem Lett 14: 187-90 (2003)
BindingDB Entry DOI: 10.7270/Q2HM57VG |
More data for this Ligand-Target Pair | |
Proto-oncogene tyrosine-protein kinase Src
(Homo sapiens (Human)) | BDBM50137576
(3-[1-{3-[3-(4-Hydroxy-piperidin-1-yl)-propyl]-4,5,...)Show SMILES CNS(=O)(=O)c1ccc2NC(=O)\C(=C/c3[nH]c4CCCCc4c3CCCN3CCC(O)CC3)c2c1 Show InChI InChI=1S/C26H34N4O4S/c1-27-35(33,34)18-8-9-24-21(15-18)22(26(32)29-24)16-25-20(19-5-2-3-7-23(19)28-25)6-4-12-30-13-10-17(31)11-14-30/h8-9,15-17,27-28,31H,2-7,10-14H2,1H3,(H,29,32)/b22-16- | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| PubMed
| n/a | n/a | 900 | n/a | n/a | n/a | n/a | n/a | n/a |
SUGEN, Inc.
Curated by ChEMBL
| Assay Description Inhibitory activity against cellular Src protein tryrosine kinase using the actin ring assay |
Bioorg Med Chem Lett 14: 187-90 (2003)
BindingDB Entry DOI: 10.7270/Q2HM57VG |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Yes
(Homo sapiens (Human)) | BDBM50137576
(3-[1-{3-[3-(4-Hydroxy-piperidin-1-yl)-propyl]-4,5,...)Show SMILES CNS(=O)(=O)c1ccc2NC(=O)\C(=C/c3[nH]c4CCCCc4c3CCCN3CCC(O)CC3)c2c1 Show InChI InChI=1S/C26H34N4O4S/c1-27-35(33,34)18-8-9-24-21(15-18)22(26(32)29-24)16-25-20(19-5-2-3-7-23(19)28-25)6-4-12-30-13-10-17(31)11-14-30/h8-9,15-17,27-28,31H,2-7,10-14H2,1H3,(H,29,32)/b22-16- | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| PubMed
| n/a | n/a | 10 | n/a | n/a | n/a | n/a | n/a | n/a |
SUGEN, Inc.
Curated by ChEMBL
| Assay Description Inhibitory activity against Yes tyrosine kinase |
Bioorg Med Chem Lett 14: 187-90 (2003)
BindingDB Entry DOI: 10.7270/Q2HM57VG |
More data for this Ligand-Target Pair | |