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Synthesis and cytotoxicity studies of new cryptophycin analogues.

机译:新型隐藻霉素类似物的合成和细胞毒性研究。

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摘要

Two analogues of cryptophycin were synthesized and biologically evaluated for their in-vitro cytotoxicities against several solid tumors and leukemia cell lines. The results revealed that both analogues exhibited a broad range of cytotoxic activity with observed IC(50 )values in the muM-range, and compound 4 was more effective than compound 3 in most assays studied.
机译:合成了隐藻霉素的两个类似物,并对它们对几种实体瘤和白血病细胞系的体外细胞毒性进行了生物学评估。结果表明,两种类似物均表现出广泛的细胞毒性活性,在muM范围内观察到的IC(50)值,在大多数研究中,化合物4比化合物3更有效。

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