Chemical Structure : HDAC6 inhibitor OXHA
Catalog No.: PC-23423Not For Human Use, Lab Use Only.
OXHA is a potent selective HDAC6 inhibitor with IC50 of 3.7 nM, promotes the acetylation of α-tubulin, >40-fold selectivity over HDAC1/2/3/8.
Bulk size, bulk discount!
E-mail: sales@probechem.com
Tech Support: tech@probechem.com
OXHA is a potent selective HDAC6 inhibitor with IC50 of 3.7 nM, promotes the acetylation of α-tubulin, >40-fold selectivity over HDAC1/2/3/8.
OXHA demonstrate stronger inhibitory activity on HDAC6 than SAHA, significantly promoting α-tubulin acetylation while exerting a comparatively weaker influence on H3 acetylation.
OXHA has potent anti-proliferative activity, comparable to or slightly exceeding that of SAHA.
OXHA effectively inhibits the migratory ability of tumor cells post-irradiation.
OXHA combined IR treatment enhances micronucleus formation in tumor cells, inhibits clone formation ability of tumor cells.
M.Wt | 450.50 | |
Formula | C24H26N4O5 | |
Appearance | Solid | |
Storage |
|
|
Solubility |
10 mM in DMSO |
1. Hu H, et al. Mol Biol Rep. 2024 Nov 13;51(1):1151.
Copyright © 2022 probechem.com. All Rights Reserved. probechem Copyright