AL 8810 ethyl amide T38114
品牌 | 厂商性质 | 产地 | 货期 |
---|---|---|---|
TargetMol | 生产商 | 美国 | 现货 |
性能特点
生化试剂,可用于动物细胞实验
规格 | 价格 | 操作 |
---|---|---|
10 mg | ¥13,200.00 | 询底价 |
1 mg | ¥1,550.00 | 询底价 |
5 mg | ¥6,860.00 | 询底价 |
Product Introduction
Bioactivity
英文名: AL 8810 ethyl amide
描述: AL 8810 is an 11β-fluoro analog of prostaglandin F2α (PGF2α) which acts as a potent and selective antagonist at the FP receptor. AL 8810 ethyl amide is an analog of AL 8810 in which the C-1 carboxyl group has been modified to an N-ethyl amide. This modification is analogous to the PG N-ethyl amides, as typified by Bimatoprost, that have been introduced as alternative PG ocular hypotensive prodrugs. In contrast to AL 8810 which contracted the cat iris, AL 8810 ethyl amide showed no contraction activity at concentrations up to 10-4 M and did not antagonize the activity of PGF2α-ethanolamide in this system.
存储条件: Powder: -20°C for 3 years | In solvent: -80°C for 1 year
溶解度: Ethanol:PBS (pH 7.2)(1:2) : 0.3 mg/mL
Ethanol : 15 mg/mL
DMF : 15 mg/mL
DMSO : 10 mg/mL
关键字: AL 8810 ethyl amide | AL 8810 ethyl Amide
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注:该产品未在中华人民共和国食品药品监督管理部门申请医疗器械注册和备案,不可用于临床诊断或治疗等相关用途