Chemical Structure : Indostat
货号: PC-28756Not For Human Use, Lab Use Only.
Indostat is a potent, selective HDAC6 inhibitor with IC50 of 14.7 nM (hHDAC6), exhibiting negligible activity against hHDAC1, hHDAC8, and hHDAC10.
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Indostat is a potent, selective HDAC6 inhibitor with IC50 of 14.7 nM (hHDAC6), exhibiting negligible activity against hHDAC1, hHDAC8, and hHDAC10.
Indostat (1-50 uM) increases α-tubulin acetylation over histone H3 acetylation in SH-SY5Y cells.
Indostat (0.1-20 uM) markedly attenuates poly I:C–induced inflammation quantified by measuring IL-6 secretion in hippocampal neuronal cells.
Indostat shows anti-inflammatory efficacy comparable to the pan-HDAC inhibitor SAHA, but with improved cellular tolerability.
| 分子量 | 422.44 | |
| 分子式 | C22H22N4O5 | |
| 外观性状 | Solid | |
| 储存条件 |
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| Solubility |
10 mM in DMSO |
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1. Fontana A, et al. Eur J Med Chem. 2026 Nov 7;321(Pt 3):119496.
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