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Antitumor agents. 258. Syntheses and evaluation of dietary antioxidant – taxoid conjugates as novel cytotoxic agents

机译:抗肿瘤药。 258.饮食抗氧化剂–紫杉类共轭物作为新型细胞毒剂的合成与评价

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摘要

Various dietary antioxidants, including vitamins, flavonoids, curcumin, and a coumarin, were conjugated with paclitaxel (>1) through an ester linkage. The newly synthesized compounds were evaluated for cytotoxic activity against several human tumor cell lines as well as the corresponding normal cell lines. Interestingly, most tested conjugates selectively inhibited the growth of 1A9 (ovarian) and KB (nasopharyngeal) tumor cells without activity against other cell lines. Particularly, conjugates >16 and >20 were highly active against 1A9 (ED50 value of 0.005 μg/mL) as well as KB (ED50 values of 0.005 and 0.14 μg/mL, respectively) cells. Compound >22b, the glycinate ester salt of vitamin E conjugated with >1, appears to be a promising lead for further development as a clinical trial candidate as it exhibited strong inhibitory activity against Panc-1 (pancreatic cancer) with less effect on the related E6E7 (normal) cell line.
机译:各种饮食抗氧化剂,包括维生素,类黄酮,姜黄素和香豆素,都通过酯键与紫杉醇(> 1 )结合。评价了新合成的化合物对几种人肿瘤细胞系以及相应的正常细胞系的细胞毒活性。有趣的是,大多数测试的结合物选择性抑制1A9(卵巢)和KB(鼻咽)肿瘤细胞的生长,而没有针对其他细胞系的活性。特别是,结合物> 16 和> 20 对1A9(ED50值为0.005μg/ mL)和KB(ED50分别为0.005和0.14μg/ mL)具有高活性) 细胞。化合物> 22b 是与> 1 结合的维生素E的甘氨酸酯盐,由于对Panc具有强抑制活性,因此有望作为进一步开发作为临床试验候选物的有希望的线索。 -1(胰腺癌)对相关E6E7(正常)细胞系的影响较小。

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