S85043 |
Alda-1 |
源叶(MedMol) | 99% |
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- 产品描述: Alda 1是一种ALDH2激动剂,能激活野生型ALDH2 (ALDH2*1)和ALDH2*2的催化活性
- 靶点: ALDH2;Apoptosis;Dehydrogenase
- 体外研究:
Alda-1 alleviated liver injury after hepatic I/R. Pretreatment with Alda-1 significantly alleviated I/R-induced elevations of alanine aminotransferase and aspartate aminotransferase, and significantly blunted the pathological injury of the liver. Moreover, Alda-1 significantly inhibited ROS and proinflammatory cytokines production, 4-HNE and MDA accumulation, and apoptosis. Increased ALDH2 activity was found after Alda-1 administration. No significant changes in ALDH2 expression were observed after I/R
- 细胞实验: Cell lines: normal rat hepatocyte cell (BRL-3A) Concentrations: 20 μM Incubation Time: 1 hour Method: The H/R (Hypoxia/reoxygenation) group cells are incubated under a hypoxic atmosphere (95% N2+5% CO2) for 6 h followed by 120 min reoxygenation (95% air + 5% CO2). The control incubation is normoxic conditions (95% air + 5% CO2) for the entire experiment. In the H/R+Alda-1 group, cells are incubated with Alda-1 (20 μM) for 60 min at 37℃ (95% air/5% CO2) before exposure to hypoxia. Furthermore, BRL-3A cells are treated with 5 μM 4-HNE for 60min before exposure to hypoxia to estimate whether 4-HNE could affect H/R.
- 动物实验: Animal Models: Male Sprague-Dawley rats (IR model) Dosages: 10 mg/kg Administration: i.p.
- 参考文献:
1. Samantha Perez-Miller, et al. Alda-1 is an agonist and chemical chaperone for the common human aldehyde dehydrogenase 2 variant. Nat Struct Mol Biol. 2010, 17(2): 159-164. 2. Zhang T, et al. Alda-1, an ALDH2 activator, protects against hepatic ischemia/reperfusion injury in rats via inhibition of oxidative stress. Free Radic Res. 2018, 52(6):629-638.
- 溶解性: Soluble in DMSO
- 保存条件: 2-8℃
- 配置溶液浓度参考:
1mg 5mg 10mg 1 mM 3.085 ml 15.424 ml 30.849 ml 5 mM 0.617 ml 3.085 ml 6.17 ml 10 mM 0.308 ml 1.542 ml 3.085 ml 50 mM 0.062 ml 0.308 ml 0.617 ml
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本计算器可帮助您计算出特定溶液中溶质的质量、溶液浓度和体积之间的关系,公式为:
质量 (mg) = 浓度 (mM) x 体积 (mL) x 分子摩尔量 (g/mol)