巴嗪普令 T67789
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 | CAS号 | 价格 | 操作 |
---|---|---|---|
500 mg | 94011-82-2 | ¥19,800.00 | 询底价 |
10 mg | 94011-82-2 | ¥3,820.00 | 询底价 |
5 mg | 94011-82-2 | ¥2,680.00 | 询底价 |
100 mg | 94011-82-2 | ¥10,500.00 | 询底价 |
25 mg | 94011-82-2 | ¥5,770.00 | 询底价 |
1 mg | 94011-82-2 | ¥1,060.00 | 询底价 |
1 mL | 94011-82-2 | ¥2,380.00 | 询底价 |
50 mg | 94011-82-2 | ¥7,740.00 | 询底价 |
Product Introduction
Bioactivity
英文名: Bazinaprine
描述: Bazinaprine 是一种选择性的、可逆的单胺氧化酶抑制剂(MAOI),是治疗抑郁症的候选化合物。Bazinaprine 对A 型单胺氧化酶显示出较强的抑制作用,对b 型单胺氧化酶只显示出较弱的抑制作用。Bazinaprine 在体内可逆,但在体外不可逆。
体外活性: Bazinaprine(SR 95191) inhibits MAO-A in a time-dependent manner in vitro and appears to be irreversible.[1] The inhibition of brain MAO-A, but not MAO-B, by SR 95191 was time dependent, with a 19-fold decrease in the IC50 values being observed over a 30-min incubation period (140 to 7.5 μM).[2]
体内活性: Bazinaprine (1–100 mg/kg, p.o.) antagonized, in a dose-dependent fashion, the irreversible inhibition of brain and liver MAO-A induced by phenelzine.[2]
存储条件: Powder: -20°C for 3 years | In solvent: -80°C for 1 year
溶解度: DMSO : 22.5 mg/mL (72.73 mM)
关键字: SR 95191 | Bazinaprine
相关产品: Cassiaside B2 | Tetrahydroharmine | Lazabemide hydrochloride | 4'-Demethyleucomin | CX-157 | 2614W94 | Paeonol | Fabomotizole hydrochloride | RN-1 dihydrochloride | Dihydroevocarpine
相关库: Anti-Neurodegenerative Disease Compound Library | Mitochondria-Targeted Compound Library | Bioactive Compounds Library Max | Neuronal Signaling Compound Library | Inhibitor Library | Bioactive Compound Library
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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