SIRT-IN-1 is a potent inhibitor of SIRT1/2/3, with IC 50 s of 15, 10, 33 μM, respectively.
性状
Solid
IC50 & Target[1][2]
SIRT1 15 nM (IC50) SIRT2 10 nM (IC50
体外研究(In Vitro)
SIRT-IN-1 (compound 28) is one of the most potent truncated pan SIRT1/ 2/3 inhibitor, the IC50 values are 0.015, 0.010, 0.033 μM, respectively. SIRT-IN-1 (SIRT1/2/3 pan inhibitor) binds identically in the catalytic active site (RMS=0.29 ?), occupying the nicotinamide C-pocket and acetyl lysine substrate channel. has not independently confirmed the accuracy of these methods. They are for reference only.
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
4°C, protect from light In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
参考文献
[1]. Disch JS, et al. Discovery of thieno[3,2-d]pyrimidine-6-carboxamides as potent inhibitors of SIRT1, SIRT2, and SIRT3. J Med Chem. 2013 May 9;56(9):3666-79.
溶解度数据
In Vitro: DMSO : 19.23 mg/mL (49.37 mM; ultrasonic and warming and heat to 60°C)配制储备液