BDBM50328409 (Z)-3-((4-(3-(dimethylamino)propoxy)-3-methylazulen-1-yl)methylene)-1H-pyrrolo[2,3-b]pyridin-2(3H)-one::CHEMBL1258376
SMILES: CN(C)CCCOc1ccccc2c(\C=C3/C(=O)Nc4ncccc34)cc(C)c12
InChI Key: InChIKey=BOGKUOUVWUICFV-HKWRFOASSA-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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Receptor-type tyrosine-protein kinase FLT3 (Homo sapiens (Human)) | BDBM50328409 ((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 Similars | Article PubMed | n/a | n/a | 1.46E+3 | 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 |