Dacinostat

404951-53-7

C22H25N3O3

DMSO : >= 43 mg/mL (113.32 mM)

Autophagy; Epigenetics; Cell Cycle/DNA Damage

Dacinostat is a potent HDAC inhibitor, with an IC₅₀ of 32 nM; Dacinostat also inhibits HDAC1 with an IC₅₀ of 9 nM, and used in cancer research. IC50 & Target: IC50: 32 nM (HDAC)^[1], 9 nM (HDAC1)^[2] In Vitro: Dacinostat (NVP-LAQ824) activates p21 promoter, with AC₅₀ of 0.30 uM. NVP-LAQ824 inhibits tumor cell (H1299, HCT116) growth, with IC₅₀s of 150 and 10 nM, respectively. NVP-LAQ824 also shows inhibitory activities against two prostate cancer cell lines (DU145 and PC3) and a breast cancer line (MDA435), with IC₅₀s of 18, 23, 39 nM, respectively. Continuous exposure of NVP-LAQ824 for 72 h produces LD90s of 0.09 M in HCT116 cells and 0.47 M in A549 cells. NVP-LAQ824 treatment of NDHF cells causes the expected G1-S growth arrest in addition to a significant reduction of cells in S-phase and accumulation of cells at the G2-M checkpoint. NVP-LAQ824 induces apoptotic death in human tumor cells. NPV-LAQ824 increases acetylation of histones H3 and H4^[1]. Dacinostat inhibits HDAC1 with an IC₅₀ of 9 nM^[2]. Dacinostat (10 and 20 nM) suppresses proliferation of AML fusion protein-expressing 32D cells. Dacinostat impairs short-term engraftment potential of leukemic stem cells. Dacinostat exhausts in vitro self-renewal potential of murine AML1/ETO- and PLZF/RARalpha-positive HSC^[3]. In Vivo: NVP-LAQ824 produces a dose-dependent inhibition of tumor growth, and at 100 mg/kg, its antitumor effect is similar to that of 5-Fluorouracil^[1].