Size: | Price | Quantity | |
---|---|---|---|
20 mg | $40.00 | ||
100 mg | $90.00 |
HPA (96017-59-3) is a histone deacetylase (HDAC) inhibitor, IC50=13 μM.1 More potent and robust than valproic acid at inducing histone hyperacetylation (600% at 50 μM), HSP70 induction and protection against glutamate excitotoxicity in cultured neurons.2 Cell permeable.
References/Citations:
1) Eikel et al. (2006), Teratogenic effects mediated by inhibition of histone deacetylases: evidence from quantitative structure activity relationships of 20 valproic acid derivatives; Chem. Res. Toxicol., 19 272
2) Leng et al. (2010), Potent neuroprotective effects of novel structural derivatives of valproic acid: potential roles of HDAC inhibition and HSP70 induction; Neurosci. Lett., 476 127
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HPA (96017-59-3) is a histone deacetylase (HDAC) inhibitor, IC50=13 μM.1 More potent and robust than valproic acid at inducing histone hyperacetylation (600% at 50 μM), HSP70 induction and protection against glutamate excitotoxicity in cultured neurons.2 Cell permeable.
References/Citations:
1) Eikel et al. (2006), Teratogenic effects mediated by inhibition of histone deacetylases: evidence from quantitative structure activity relationships of 20 valproic acid derivatives; Chem. Res. Toxicol., 19 272
2) Leng et al. (2010), Potent neuroprotective effects of novel structural derivatives of valproic acid: potential roles of HDAC inhibition and HSP70 induction; Neurosci. Lett., 476 127
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