Wall M E, Wani M C, Natschke S M, Nicholas A W
J Med Chem. 1986 Aug;29(8):1553-5. doi: 10.1021/jm00158a044.
The antitumor alkaloid 11-hydroxy-(20S)-camptothecin was isolated from the woody tissue of Camptotheca acuminata. Structural proof derived from comparison with racemic 4 prepared by total synthesis. Antitumor activity of racemic 4 in L1210 leukemia in mice was considerably greater than that of natural (20S)-camptothecin and its sodium salt. There was also no toxic effect observed even at relatively high doses.
从喜树的木质组织中分离出抗肿瘤生物碱11-羟基-(20S)-喜树碱。通过与全合成制备的外消旋体4进行比较确定其结构。外消旋体4对小鼠L1210白血病的抗肿瘤活性明显高于天然(20S)-喜树碱及其钠盐。即使在相对高剂量下也未观察到毒性作用。