首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Novel N-(phosphonomethyl) glycine derivatives: Design, characterization and biological activity.
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Novel N-(phosphonomethyl) glycine derivatives: Design, characterization and biological activity.

机译:新型N-(膦酰基甲基)甘氨酸衍生物:设计,表征和生物活性。

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摘要

A series of Calpha,alpha-disubstituted cyclic derivatives of N-(phosphonomethyl) glycine have been synthesized and characterized. They exhibited moderate clastogenicity, low antiproliferative activity on mice bone marrow cells and well expressed cytotoxicity against human tumor cell lines. The 8- and 12-membered cyclic analogs proved superior to the remaining compounds and were found to trigger apoptotic cell death in DOHH-2 cells. The latter compound caused 50% inhibition of the viability of hemobastose-derived cell lines at concentrations ranging from 20 to 67 microM.
机译:已经合成并表征了一系列的N-(膦酰基甲基)甘氨酸的Cα,α-二取代的环状衍生物。它们对小鼠骨髓细胞表现出中等的致胶裂性,低的抗增殖活性,并且对人肿瘤细胞系的表达良好。 8元和12元环状类似物被证明优于其余化合物,并被发现可引发DOHH-2细胞凋亡。后者的化合物在20至67 microM的浓度范围内,导致50%的血源性源自母糖的细胞系的活力受到抑制。

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