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去甲斑蝥素衍生物在癌细胞中的合成及抗增殖测定

Synthesis and antiproliferative assay of norcantharidin derivatives in cancer cells.

作者信息

Tu Guo Gang, Zhan Jian Feng, Lv Qiao Li, Wang Jia Qi, Kuang Bin Hai, Li Shao Hua

机构信息

Department of Medicinal Chemistry, School of Pharmaceutical Science, Nanchang University, 461, BaYi Road, NanChang, 330006, P.R. China.

出版信息

Med Chem. 2014 Jun;10(4):376-81. doi: 10.2174/15734064113099990037.

Abstract

Diels-Alder reaction between furan and maleic anhydride resulted in 5,6-dehydro norcantharidin, then norcantharidin was obtained by reduction. The substituted-carboxylic acid was condensed with N-aminothiourea in presence of phosphorus oxychloride, yielding 2-amino-1,3,4-thiadiazole derivatives. Novel norcantharidin derivatives were synthesized with acylation, then intramolecular condensation using norcantharidin (or 5,6-dehydro norcantharidin) and 2-amino- 1,3,4-thiadiazole derivatives. All the target compounds were confirmed by IR, (1)HNMR, ESI-MS and were reported for the first time. Norcantharidin derivatives antiproliferative assay was tested by MTT method against A549 and PC-3 cell lines. The results showed that all the norcantharidin derivatives displayed moderate inhibitory activities.

摘要

呋喃与马来酸酐之间发生狄尔斯-阿尔德反应生成5,6-脱氢去甲斑蝥素,然后通过还原得到去甲斑蝥素。取代羧酸在三氯氧磷存在下与N-氨基硫脲缩合,生成2-氨基-1,3,4-噻二唑衍生物。用去甲斑蝥素(或5,6-脱氢去甲斑蝥素)与2-氨基-1,3,4-噻二唑衍生物通过酰化反应,然后进行分子内缩合反应合成了新型去甲斑蝥素衍生物。所有目标化合物均通过红外光谱、核磁共振氢谱、电喷雾质谱进行了确证,且均为首次报道。采用MTT法对去甲斑蝥素衍生物进行了抗增殖活性检测,检测对象为A549和PC-3细胞系。结果表明,所有去甲斑蝥素衍生物均表现出中等程度的抑制活性。

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