Found 4 hits for monomerid = 50207497 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 |
Mast/stem cell growth factor receptor Kit
(Homo sapiens (Human)) | BDBM50207497
(1-(4-(3-amino-7-(2-(pyrrolidin-1-yl)ethoxy)-1H-ind...)Show SMILES Cc1cccc(NC(=O)Nc2ccc(cc2)-c2ccc(OCCN3CCCC3)c3[nH]nc(N)c23)c1 Show InChI InChI=1S/C27H30N6O2/c1-18-5-4-6-21(17-18)30-27(34)29-20-9-7-19(8-10-20)22-11-12-23(25-24(22)26(28)32-31-25)35-16-15-33-13-2-3-14-33/h4-12,17H,2-3,13-16H2,1H3,(H3,28,31,32)(H2,29,30,34) | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 26 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description Inhibition of c-Kit by HTRF assay |
J Med Chem 50: 1584-97 (2007)
Article DOI: 10.1021/jm061280h BindingDB Entry DOI: 10.7270/Q2DJ5F95 |
More data for this Ligand-Target Pair | |
Mast/stem cell growth factor receptor Kit
(Homo sapiens (Human)) | BDBM50207497
(1-(4-(3-amino-7-(2-(pyrrolidin-1-yl)ethoxy)-1H-ind...)Show SMILES Cc1cccc(NC(=O)Nc2ccc(cc2)-c2ccc(OCCN3CCCC3)c3[nH]nc(N)c23)c1 Show InChI InChI=1S/C27H30N6O2/c1-18-5-4-6-21(17-18)30-27(34)29-20-9-7-19(8-10-20)22-11-12-23(25-24(22)26(28)32-31-25)35-16-15-33-13-2-3-14-33/h4-12,17H,2-3,13-16H2,1H3,(H3,28,31,32)(H2,29,30,34) | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 26 | n/a | n/a | n/a | n/a | n/a | n/a |
Punjabi University
Curated by ChEMBL
| Assay Description Inhibition of c-Kit by HTRF method |
Eur J Med Chem 45: 393-404 (2010)
Article DOI: 10.1016/j.ejmech.2009.09.013 BindingDB Entry DOI: 10.7270/Q2RX9C6D |
More data for this Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50207497
(1-(4-(3-amino-7-(2-(pyrrolidin-1-yl)ethoxy)-1H-ind...)Show SMILES Cc1cccc(NC(=O)Nc2ccc(cc2)-c2ccc(OCCN3CCCC3)c3[nH]nc(N)c23)c1 Show InChI InChI=1S/C27H30N6O2/c1-18-5-4-6-21(17-18)30-27(34)29-20-9-7-19(8-10-20)22-11-12-23(25-24(22)26(28)32-31-25)35-16-15-33-13-2-3-14-33/h4-12,17H,2-3,13-16H2,1H3,(H3,28,31,32)(H2,29,30,34) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 120 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description Inhibition of FLT3 by HTRF assay |
J Med Chem 50: 1584-97 (2007)
Article DOI: 10.1021/jm061280h BindingDB Entry DOI: 10.7270/Q2DJ5F95 |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50207497
(1-(4-(3-amino-7-(2-(pyrrolidin-1-yl)ethoxy)-1H-ind...)Show SMILES Cc1cccc(NC(=O)Nc2ccc(cc2)-c2ccc(OCCN3CCCC3)c3[nH]nc(N)c23)c1 Show InChI InChI=1S/C27H30N6O2/c1-18-5-4-6-21(17-18)30-27(34)29-20-9-7-19(8-10-20)22-11-12-23(25-24(22)26(28)32-31-25)35-16-15-33-13-2-3-14-33/h4-12,17H,2-3,13-16H2,1H3,(H3,28,31,32)(H2,29,30,34) | 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 | 31 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description Inhibition of VEGF-induced human KDR phosphorylation in mouse 3T3 cells by ELISA |
J Med Chem 50: 1584-97 (2007)
Article DOI: 10.1021/jm061280h BindingDB Entry DOI: 10.7270/Q2DJ5F95 |
More data for this Ligand-Target Pair | |