Synthesis of 4α-Methyl-Δ<sup>7</sup>-steroiäs. The Interrelationship of Cholesterol, Citrostadienol and Lophenol
作者:Yehuda Mazur、Franz Sondheimer
DOI:10.1021/ja01556a033
日期:1958.12
Synthesis and antitumor activity of cholest-4α-methyl-7-en-3β-ol derivatives
作者:Lan He、Yumei Liu、Jiangong Shi、Qiang Pei
DOI:10.1016/j.steroids.2006.01.006
日期:2006.6
Cholest-4 alpha-methyl-7-en-3 beta-ol (1) has potent inhibitory activity against pc 12 tumor with 0.5043 ratio (10 mu g/mL). This paper describes a series of structural modification of this compound, which focus on 3 beta-hydroxyl group and 7(8)-double bond. The synthesized derivatives of I were tested for human cancer cell lines including colon cancer (HCT-8), liver cancer (BEL-7402) and nasopharyngeal cancer (KB) cells. The results showed that cholest-4 alpha-methyl-8-en-3 beta,7 alpha-diol 6a inhibits KB cell significantly with IC50 1.32 x 10(-9) mu g/ml. In addition, the cytotoxic properties of this compound against HCT-8 and BEL-7402 are excellent with IC50 1.2 mu g/mL. (c) 2006 Elsevier Inc. All rights reserved.
The Neutral Constituents of the Cactus Lophocereus schottii. The Structure of Lophenol--4α-Methyl-Δ<sup>7</sup>-cholesten-3β-ol--A Link in Sterol Biogenesis<sup>1-3</sup>
作者:Carl Djerassi、G. W. Krakower、A. J. Lemin、Liang H. Liu、J. S. Mills、R. Villotti