首页> 外文期刊>Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry >SEMISYNTHESIS OF TRIPTOLIDE ANALOGUES PART IV: EFFECTS OF C-14 CARBAMOTHIOATE SUBSTITUENTS ON CYTOTOXIC ACTIVITIES
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SEMISYNTHESIS OF TRIPTOLIDE ANALOGUES PART IV: EFFECTS OF C-14 CARBAMOTHIOATE SUBSTITUENTS ON CYTOTOXIC ACTIVITIES

机译:雷公藤内酯类似物第四部分的半合成:C-14氨基甲酯取代基对细胞毒性活性的影响

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摘要

Four C-14 carbamothioate triptolide analogues were prepared and their cytotoxic activities on A549 human lung tumor cells and HT29 human colon tumor cells were evaluated. The activities of the prepared compounds were weaker than those of the parent compound, triptolide (1). However, some differences were noted in the activities of prepared compounds. The leaving ability and bulkiness of the amine components of their carbamothioate groups appeared to affect their cytotoxic activities.
机译:制备了四种C-14氨基甲基氨基甲酸酯类似物,并评估了对A549人肺肿瘤细胞和HT29人结肠肿瘤细胞的细胞毒性活性。 制备的化合物的活性比母体化合物,雷公酮(1)的活性较弱。 然而,在制备的化合物的活性中注意到了一些差异。 其氨基甲酸酯基团的胺组分的留下能力和膨胀性似乎影响了它们的细胞毒性活性。

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