For research use only. Not for therapeutic Use.
HDAC-IN-40 is a potent alkoxyamide-based HDAC inhibitor with Ki values of 60 nM and 30 nM for HDAC2 and HDAC6, respectively. HDAC-IN-40 had antitumor effects[1].
HDAC-IN-40 (Compound 13d) shows antiproliferative activity against the cell line A2780 and Cal27 with IC50 values of 0.89 µM and 0.72 µM, respectively[1].
HDAC-IN-40 induces accumulation of acetyl α-tubulin in Cal27 and Cal27CisR[1].
HDAC-IN-40 enhances the Cisplatin-induced cytotoxicity via caspase-3/7 activation[1].
Catalog Number | I043566 |
CAS Number | 2463198-51-6 |
Synonyms | N-[6-(hydroxyamino)-6-oxohexoxy]-3,5-dimethoxybenzamide |
Molecular Formula | C15H22N2O6 |
Purity | ≥95% |
InChI | InChI=1S/C15H22N2O6/c1-21-12-8-11(9-13(10-12)22-2)15(19)17-23-7-5-3-4-6-14(18)16-20/h8-10,20H,3-7H2,1-2H3,(H,16,18)(H,17,19) |
InChIKey | WARMWIVORGODLX-UHFFFAOYSA-N |
SMILES | COC1=CC(=CC(=C1)C(=O)NOCCCCCC(=O)NO)OC |
Reference | [1]. Yodita Asfaha, et al. Novel alkoxyamide-based histone deacetylase inhibitors reverse cisplatin resistance in chemoresistant cancer cells. Bioorg Med Chem. 2020 Jan 1;28(1):115108. |