环己胺
亚精胺
化学
腐胺
酶抑制剂
非竞争性抑制
生物化学
立体化学
ATP合酶
酶
有机化学
作者
Akira Shirahata,Toru Morohoshi,Keijiro Samejima
出处
期刊:Chemical & Pharmaceutical Bulletin
[Pharmaceutical Society of Japan]
日期:1988-01-01
卷期号:36 (8): 3220-3222
被引量:26
摘要
Trans-4-methylcyclohexylamine was found to inhibit pig spermidine synthase potently in assay conditions containing 50 μM of decarboxylated S-adenosylmethionine. It showed 50% inhibition at 1.7 μM compared to 8.1 μM for cyclohexylamine, and 2.5 μM for S-adenosyl-1, 8-diamino-3-thiooctane, known as the most potent inhibitor. The inhibition was competitive with putrescine, similar to cyclohexylamine, and the Ki was 40 nM.
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