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二叶亭 4-C 衍生物的合成及初步抗癌活性评价。

Synthesis and Preliminary Anticancer Evaluation of 4-C Derivatives of Diphyllin.

机构信息

School of Pharmacy, China Pharmaceutical University, Nanjing, China.

School of Pharmacy, Nantong University, Nantong, China.

出版信息

Chem Biol Drug Des. 2024 Sep;104(3):e14635. doi: 10.1111/cbdd.14635.

Abstract

The natural lignan diphyllin has shown promising antitumor activity, although its clinical advancement has been impeded by challenges such as low solubility, poor metabolic stability, and limited potency. In response, we developed and synthesized two sets of diphyllin 4-C derivatives, comprising six ester derivatives and eight 1, 2, 3-triazole derivatives. Notably, among these derivatives, 1, 2, 3-triazole derivatives 7c and 7e demonstrated the most potent cytotoxic effects, with IC values ranging from 0.003 to 0.01 μM. Treatment with 0.2 μM of 7c and 7e resulted in a reduction of V-ATPase activity in HGC-27 cells to 23% and 29%, respectively.

摘要

天然木脂素二氢菲具有良好的抗肿瘤活性,但由于溶解度低、代谢稳定性差、效力有限等问题,其临床应用受到阻碍。针对这些问题,我们设计并合成了两组二氢菲 4-C 衍生物,包括 6 个酯衍生物和 8 个 1,2,3-三唑衍生物。值得注意的是,在这些衍生物中,1,2,3-三唑衍生物 7c 和 7e 表现出最强的细胞毒性作用,IC 值范围在 0.003 到 0.01μM 之间。用 0.2μM 的 7c 和 7e 处理 HGC-27 细胞,可使 V-ATPase 活性分别降低 23%和 29%。

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