Alda 1 is a cell-permeable benzamide compound that selectively enhances the activity of both the wild-type ALDH2*1 and the east asian E487K mutant ALDH2*2 forms of mitochondrial aldehyde dehydrogenase 2 (2.1-, 2.2, and 11-fold activation of 20 g wt homo, wt/mut hetero, and mut homo tetramer, respectively, at 100 M), while exhibiting no effect toward alcohol dehydrogenase 1, cytosolic ALDH1, or mitochondrial ALDH5.
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化学信息
名称 | Alda 1 |
Iupac 化学名称 | N-(1,3-Benzodioxol-5-ylmethyl)-2,6-dichlorobenzamide |
同义词 | ALDH2 Agonist |
英文同义词 | ALDH2 Agonist |
分子式 | C15H11Cl2NO3 |
分子量 | 324.159 |
Smile | O1COC2=C1C=CC(=C2)CNC(C2=C(C=CC=C2Cl)Cl)=O |
InChiKey | NMKJFZCBCIUYHI-UHFFFAOYSA-N |
InChi | InChI=1S/C15H11Cl2NO3/c16-10-2-1-3-11(17)14(10)15(19)18-7-9-4-5-12-13(6-9)21-8-20-12/h1-6H,7-8H2,(H,18,19) |
Cas号 | 349438-38-6 |
相关CAS号 | |
外观性状 | Solid powder |
纯度 | 98% |
存储 | -20 ºC for 3 years |
可溶性 | Soluble in DMSO |
处理方式 | |
运输条件 | Shipped under ambient temperature |
海关编码 | |
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Mechanism | |
Cell study | |
Animal study | |
Clinical study | |