BDBM50328406 (Z)-3-((4-(3-(dimethylamino)propoxy)-3-methylazulen-1-yl)methylene)-5-fluoroindolin-2-one::CHEMBL1258150
SMILES: CN(C)CCCOc1ccccc2c(\C=C3/C(=O)Nc4ccc(F)cc34)cc(C)c12
InChI Key: InChIKey=YMXYPDNRDMMODA-STZFKDTASA-N
Data: 1 IC50
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 |
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Receptor-type tyrosine-protein kinase FLT3 (Homo sapiens (Human)) | BDBM50328406 ((Z)-3-((4-(3-(dimethylamino)propoxy)-3-methylazule...) | 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 | 12 | n/a | n/a | n/a | n/a | n/a | n/a |
Industrial Technology Research Institute Curated by ChEMBL | Assay Description Inhibition of FLT3 by time resolved fluorescence method | Bioorg Med Chem Lett 20: 6129-32 (2010) Article DOI: 10.1016/j.bmcl.2010.08.025 BindingDB Entry DOI: 10.7270/Q2N29X51 | |||||||||||
More data for this Ligand-Target Pair |