SirtAct (CAY-10591)
-
- 应用范围
- Inhibition (Inh)
- 原理
- SIRT1 activator
- 产品特性
- Sirt1 activator (233 % at 10 μM)1 Suppresses TNFα release from THP-1 cells and stimulates adipogenesis in 3T3L1 cells. SIRT1 stimulation by SirtAct leads to decreased tissue factor mediated thrombogenicity in mice. Inhibits NFκB activation and reduces inflammatory cytokine production in lamina propria mononuclear cells from IBD patients. Prevents and cures experimental colitis in a mouse model.
- 纯度
- >98 %
- Chemical Name
- 2-Amino-N-cyclopentyl-1-(3-methoxypropyl)-1H-pyrrolo[2,3-b]quinoxaline-3-carboxamide
- Formula
- C20H25N5O2
- Solubility
- Soluble in DMSO (up to 50 mg/ml) or in Ethanol (up to 20 mg/ml).
-
-
- 限制
- 仅限研究用
-
- 状态
- Powder
- 储存条件
- -20 °C
-
- 背景
- CAY10591,Posttranslational modification,Epigenetics,Chromatin,Protein deacetylase,Diabetes,Inflammation,Cytokine,NFkappaB
- 分子量
- 367.46
- CAS-编号
- 839699-72-8
-