BDBM389562 N'-{6-bromo-2-[(E)-2-(4- fluorophenyl)vinyl]quinazolin-4-yl}- N,N-dimethylpropane-1,3-diamine::US9951029, 15
SMILES: CN(C)CCCNc1nc(\C=C\c2ccc(F)cc2)nc2ccc(Br)cc12
InChI Key: InChIKey=PWQCUQXKJUPYKG-IZZDOVSWSA-N
Data: 2 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)) | BDBM389562 (N'-{6-bromo-2-[(E)-2-(4- fluorophenyl)vinyl]quinaz...) | PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | Article PubMed | n/a | n/a | 1.51E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Vichem Chemie Research Ltd Curated by ChEMBL | Assay Description Inhibition of FLT3 ITD mutant (unknown origin) using TAMRA-Src-tide as substrate measured after 1 hr in presence of ATP at its Km concentration by IM... | Eur J Med Chem 184: (2019) Article DOI: 10.1016/j.ejmech.2019.111710 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Receptor-type tyrosine-protein kinase FLT3 (Homo sapiens (Human)) | BDBM389562 (N'-{6-bromo-2-[(E)-2-(4- fluorophenyl)vinyl]quinaz...) | PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 1.55E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Georgia Institute of Technology | Assay Description FLT3(ITD) biochemical assays were performed on two different assay system platforms, using TranscreenerŽ ADP Assay FP method (BellBrook Labs, Madison... | J Med Chem 52: 456-68 (2009) BindingDB Entry DOI: 10.7270/Q2NG4T0S | |||||||||||
More data for this Ligand-Target Pair |