CAS NO: | 49843-98-3 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
5mg | 电议 |
10mg | 电议 |
25mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
500mg | 电议 |
生物活性 | Selisistat (EX-527) is a potent and selectiveSirT1(Sir2 in Drosophila melanogaster) inhibitor with anIC50of 123 nM forSirT1. Selisistat alleviates pathology in multiple animal and cell models of Huntington's disease[1][2]. | ||||||||||||||||
IC50& Target | IC50: 123 nM (SirT1)[2] | ||||||||||||||||
体外研究 (In Vitro) | Selisistat (1-10 μM) inhibits the deacetylation activity of both human SirT1 and Drosophila Sir2 in transfected cells[1]. | ||||||||||||||||
体内研究 (In Vivo) | Selisistat (5 and 20 mg/kg, PO, daily; transgenic R6/2 mice beginning at 4.5 weeksof age to death) is protective in the R6/2 mouse model of Huntington’s disease (HD)[1]. | ||||||||||||||||
Clinical Trial | |||||||||||||||||
分子量 | 248.71 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C13H13ClN2O | ||||||||||||||||
CAS 号 | 49843-98-3 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 |
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溶解性数据 | In Vitro: DMSO : ≥ 100 mg/mL(402.07 mM) *"≥" means soluble, but saturation unknown. 配制储备液
* 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 In Vivo: 请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照In Vitro方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用;
以下溶剂前显示的百
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