Synthesis and antiproliferative activity of 7-substituted amide estradiol derivatives

IF 2.6 4区 医学 Q3 CHEMISTRY, MEDICINAL Medicinal Chemistry Research Pub Date : 2024-09-16 DOI:10.1007/s00044-024-03301-4
Chun-Fang Gan, Ying Li, Hua-Long Chen, Jia-Wei Yao, Yun-Qiong Gu, Bin Su, Zhi-Wei Zhong, Jian-Guo Cui, Yan-Min Huang, Zhi-Ping Liu
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Abstract

The modification of the 7-position in the estradiol structure has drawn significant attention from pharmacologists. In this paper, we synthesize various amine derivatives of estradiol, functionalized with a side chain at the 7-position. The anti-tumor activities of target compounds were evaluated using MTT assay. As the side chain is alkyl amides or halogen atoms substituted alkyl amine, the compounds exhibit excellent activity, with short chains being more active than long chains. Additionally, we studied the antitumor mechanism of the 7-substituted estradiol amide compounds. Compounds 9o can effectively inhibit the proliferation and migration of MCF-7 cells and induce early apoptosis in breast cancer tumors under certain concentration conditions.

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7 取代酰胺类雌二醇衍生物的合成和抗增殖活性
雌二醇结构中 7-位的修饰引起了药理学家的极大关注。在本文中,我们合成了多种雌二醇胺衍生物,这些衍生物在 7 位上具有侧链功能。采用 MTT 法评估了目标化合物的抗肿瘤活性。由于侧链是烷基酰胺或卤素原子取代的烷基胺,这些化合物表现出优异的活性,其中短链的活性高于长链。此外,我们还研究了 7-取代雌二醇酰胺化合物的抗肿瘤机理。在一定浓度条件下,化合物 9o 能有效抑制 MCF-7 细胞的增殖和迁移,并诱导乳腺癌肿瘤早期凋亡。
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来源期刊
Medicinal Chemistry Research
Medicinal Chemistry Research 医学-医药化学
CiteScore
4.70
自引率
3.80%
发文量
162
审稿时长
5.0 months
期刊介绍: Medicinal Chemistry Research (MCRE) publishes papers on a wide range of topics, favoring research with significant, new, and up-to-date information. Although the journal has a demanding peer review process, MCRE still boasts rapid publication, due in part, to the length of the submissions. The journal publishes significant research on various topics, many of which emphasize the structure-activity relationships of molecular biology.
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