SIRT-IN-1
目录号: PL11287 纯度: ≥98%
CAS No. :1431411-60-7
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中文名称
SIRT-IN-1
中文别名
4-[4-[2-[(2,2-二甲基-1-氧代丙基)氨基]乙基]-1-哌啶基]-噻吩并[3,2-d]嘧啶-6-羧酰胺
英文名称
SIRT-IN-1
英文别名
4-[4-[2-[(2,2-dimethyl-1-oxopropyl)amino]ethyl]-1-piperidinyl]-Thieno[3,2-d]pyrimidine-6-carboxamide;SIRT-IN-1;4-(4-{2-[(2,2-Dimethylpropanoyl)amino]ethyl}piperidin-1-Yl)thieno[3,2-D]pyrimidine-6-Carboxamide;4jt8;NSPKBHVNVJWICU-UHFFFAOYSA-N;BDBM50431096;Q27452272;4-[4-[2-(Pivaloylamino)ethyl]piperidino]thieno[3,2-d]pyrimidine-6-carboxamide;4-(4-(2-pivalamidoethyl)piperidin-1-yl)thieno[3,2-d]pyrimidine-6-carboxamide;1NR;Thieno[3,2-d]pyriMidine-6-carboxaMide,4-[4-[2-[(2,2-diMethyl-1-oxopropyl)aMino]eth
Cas No.
1431411-60-7
分子式
C19H27N5O2S
分子量
389.52
包装储存
4°C, protect from light In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
产品详情
SIRT-IN-1 是 SIRT1/2/3 的有效抑制剂,其 IC50 值分别为 15,10,33 μM。
生物活性
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
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1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

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