CAS NO: | 848193-68-0 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
2mg | 电议 |
5mg | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
生物活性 | (S)-Selisistat ((S)-EX-527) is a potent and selectiveSIRT1inhibitor, with anIC50of 98 nM. | ||||||||||||||||
IC50& Target[1] |
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体外研究 (In Vitro) | (S)-Selisistat is an inhibitor of SIRT1 enzymatic activity (IC50, 98 nM), identified in a high-throughput screen using bacterially expressed human SIRT1. (S)-Selisistat inhibits SIRT1 in a concentration-dependent manner with an IC50of 38 nM, in agreement with the activity on bacterially expressed SIRT1. (S)-Selisistat has much lower potency against SIRT2 (IC50, 19.6 μM) or SIRT3 (IC50, 48.7 μM) but does not inhibit class I/II HDAC activity at concentrations up to 100 μM[1]. (S)-Selisistat exerts an inhibitory effect on SIRT1 activity without affecting SIRT1 expression on both mRNA and protein levels[2]. | ||||||||||||||||
体内研究 (In Vivo) | (S)-Selisistat abolishes Resveratrol (RSV)-induced attenuation of microvascular inflammation inob/obseptic mice. Finally,ob/obmice in Sepsis+RSV group has significantly increased 7-day survival vs. Sepsis+Vehicle group[3]. | ||||||||||||||||
分子量 | 248.71 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C13H13ClN2O | ||||||||||||||||
CAS 号 | 848193-68-0 | ||||||||||||||||
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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