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修饰的紫杉醇,4. 侧链修饰的紫杉醇的合成及生物活性

Modified taxols, 4. Synthesis and biological activity of taxols modified in the side chain.

作者信息

Magri N F, Kingston D G

机构信息

Department of Chemistry, Virginia Polytechnic Institute, Blacksburg 24061.

出版信息

J Nat Prod. 1988 Mar-Apr;51(2):298-306. doi: 10.1021/np50056a017.

Abstract

A number of taxol derivatives substituted at the 2' position of the side chain have been prepared and their biological activities determined in KB cell culture and/or the P-388 in vivo assay. The 2'-(t-butyldimethylsilyl)taxol 5 is essentially inactive, indicating the need for a free hydroxyl group at the 2' position for activity. Epimerization of the 2' position occurred on treatment of 2'-acetyltaxol derivatives with 1,5-diazabicyclo[5.4.0]undec-7-ene, but treatment of 2'-(2,2,2-trichloroethyloxycarbonyl) taxol derivatives with DBU yielded the novel cyclization products 11 and 12 and, after deprotection at the 7 position, 13. The derivative 13 is also essentially inactive in the KB test system. Two taxols with increased H2O solubility were prepared, the 2'-(beta-alanyl) derivative 15 and the 2'-succinyl derivative 16. Although both these derivatives were active in vivo and in vitro, the former was too unstable and the latter not active enough to make suitable H2O-soluble derivatives of taxol.

摘要

已经制备了一些在侧链2'位被取代的紫杉醇衍生物,并在KB细胞培养和/或P - 388体内试验中测定了它们的生物活性。2' -(叔丁基二甲基甲硅烷基)紫杉醇5基本无活性,这表明2'位需要一个游离羟基才能具有活性。用1,5 - 二氮杂双环[5.4.0]十一碳 - 7 - 烯处理2' - 乙酰基紫杉醇衍生物时,2'位发生了差向异构化,但用DBU处理2' -(2,2,2 - 三氯乙氧基羰基)紫杉醇衍生物得到了新型环化产物11和12,并且在7位脱保护后得到了13。衍生物13在KB测试系统中也基本无活性。制备了两种水溶性增加的紫杉醇,即2' -(β - 丙氨酰)衍生物15和2' - 琥珀酰衍生物16。尽管这两种衍生物在体内和体外都有活性,但前者太不稳定,后者活性又不够,无法制成合适的水溶性紫杉醇衍生物。

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