刘瑞武, 尹大力, 王东辉, 李春, 郭积玉, 梁晓天. 新型14β-侧链紫杉醇衍生物的合成及构效关系研究J. 药学学报, 1998, 33(12): 910-918.
引用本文: 刘瑞武, 尹大力, 王东辉, 李春, 郭积玉, 梁晓天. 新型14β-侧链紫杉醇衍生物的合成及构效关系研究J. 药学学报, 1998, 33(12): 910-918.
Liu Ruiwu, Yin Dali, Wang Donghui, Li Chun Guo Jiyu, Liang Xiaotian, . SYNTHESIS AND STRUCTURE-ACTIVITY RELATIONSHIPS OF NOVEL 14β-SIDE CHAIN TAXOL DERIVATIVESJ. Acta Pharmaceutica Sinica, 1998, 33(12): 910-918.
Citation: Liu Ruiwu, Yin Dali, Wang Donghui, Li Chun Guo Jiyu, Liang Xiaotian, . SYNTHESIS AND STRUCTURE-ACTIVITY RELATIONSHIPS OF NOVEL 14β-SIDE CHAIN TAXOL DERIVATIVESJ. Acta Pharmaceutica Sinica, 1998, 33(12): 910-918.

新型14β-侧链紫杉醇衍生物的合成及构效关系研究

SYNTHESIS AND STRUCTURE-ACTIVITY RELATIONSHIPS OF NOVEL 14β-SIDE CHAIN TAXOL DERIVATIVES

  • 摘要: 以生物合成得到的紫杉烷 sinenxan A为起始原料,合成一系列新的紫杉醇衍生物,以寻找高效低毒、抗瘤谱广、综合性能好的新一代紫杉醇类抗癌药,并进行构效关系研究。从半合成的紫杉烷中间体7出发,分别经5步和6步反应成功地合成了4位羟基和4位乙酸酯两类共8个新的14β侧链紫杉醇衍生物,2位基团为苯甲酸酯、间氯苯甲酸酯、正戊酸酯和苯乙酸酯。将目标化合物连同已合成的2个14β-侧链紫杉醇衍生物进行了微管聚合试验和体外肿瘤细胞抑制试验。所有化合物在浓度为10μmol·L-1时对微管无作用。在体外肿瘤细胞抑制试验中,大部分化合物显示边缘细胞毒活性。14β-侧链紫杉醇衍生物的构效关系与13α-侧链紫杉醇衍生物有所不同,2位脂肪酸酯与2位芳香酸酯活性相当,表明2位基团的改变对活性无明显影响。4位羟基衍生物的活性好于4位乙酸酯。

     

    Abstract: In order to develop new generation of taxollike anticancer agents with fewer side effects, improved activity, superior pharmacological properties and broad antitumor spectrum, along with structureactivity relationship study, a series of new taxol derivatives are to be synthesized starting from sinenxan A - a biosynthetic taxane. Eight new 14β-side chain taxol derivatives with 4-OH and 4-Ac were synthesized in 5 and 6 steps from semisynthetic taxoid intermediate 7, respectively. These included taxol derivatives modified at C-2 position with benzoate, m-Cl benzoate, valerate and phenylacetate. All target compounds together with two other 14β-side chain taxol derivatives were tested in a microtubule assembly assay, and in an in vitro cytotoxicity assay (KB, A2780, HCT-8 cell line). All compounds had no effect in the microtubule assembly assay at 10 μmol·L-1. Most of them showed marginal activity in the in vitro cytotoxicity. The structureactivity relationship was different from taxol derivatives. 2-Aliphatic ester displayed similar activity to 2-aromatic ester, which indicated that the aromatic group at C-2 position was not important for cytotoxicity. Comparing among themselves, 4-OH deravitives possessed stronger activity than 4-Ac.

     

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