Dehydroabiethylamine 是肝脏 CYP2B 活性的诱导剂。 Dehydroabiethylamine 抑制丙酮酸脱氢酶激酶 (PDK) 和细胞内胆固醇转运，具有抗肿瘤活性。
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描述
Dehydroabiethylamine is an inducer of hepatic CYP2B activity. Dehydroabiethylamine inhibits pyruvate dehydrogenase kinases (PDKs) and intracellular cholesterol transport with anti-tumor activity.
Cas No.
1446-61-3
分子式
C20H31N
分子量
285.47
别名
Leelamine;Leelamine free base;NSC-2955;NSC 2955;Dehydroabietylamine;NSC2955;脱氢松香胺
储存和溶解度
DMSO:Soluble
Powder: -20°C for 3 years
In solvent: -80°C for 2 years
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