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HDAC6 inhibitor OXHA

Chemical Structure : HDAC6 inhibitor OXHA

CAS No.: 2889357-31-5

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.

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Purity & Documentation Purity: >98% (HPLC)

Biological Activity

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.

Physicochemical Properties

M.Wt 450.50
Formula C24H26N4O5
Appearance Solid
CAS No.
Storage
Solide Powder
-20°C 12 Months; 4°C 6 Months
In Solvent
-80°C 6 Months; -20°C 6 Months
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

N-(4-((7-(hydroxyamino)-7-oxoheptyl)carbamoyl)phenyl)-5-phenyloxazole-2-carboxamide

References

1. Hu H, et al. Mol Biol Rep. 2024 Nov 13;51(1):1151.

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