Gordaliza M, García P A, del Corral J M Miguel, Castro M A, Gómez-Zurita M A
Departamento de Química Farmacéutica, Facultad de Farmacia, Universidad de Salamanca, 37007 Salamanca, Spain.
Toxicon. 2004 Sep 15;44(4):441-59. doi: 10.1016/j.toxicon.2004.05.008.
Several podophyllotoxin derivatives modified in the A, B, C, D and E rings were prepared from podophyllotoxin and methyl isoxazopodophyllic acid and evaluated for their cytotoxicity on several neoplastic cell lines. Chemical transformations performed on these compounds have yielded derivatives more potent and more selective that the parent compound. Most of the compounds maintained their cytotoxicity at the microM level. Distribution, biosynthesis, production, biotechnology, applications and synthesis have also been reviewed.
从鬼臼毒素和甲基异恶唑鬼臼酸制备了几种在A、B、C、D和E环上修饰的鬼臼毒素衍生物,并评估了它们对几种肿瘤细胞系的细胞毒性。对这些化合物进行的化学转化产生了比母体化合物更有效、更具选择性的衍生物。大多数化合物在微摩尔水平上保持其细胞毒性。还综述了其分布、生物合成、生产、生物技术、应用和合成。