新型苯并[d]咪唑[2,1-b]噻唑衍生物的合成、结构表征及对MCF-7乳腺癌细胞的细胞毒活性

IF 1.8 4区 医学 Q3 PHARMACOLOGY & PHARMACY Iranian Journal of Pharmaceutical Research Pub Date : 2022-12-01 DOI:10.5812/ijpr-127041
Nahid Ahmadi, Soraya Shahhosseini, Farshad H Shirazi, Golrokh Farnam, Afshin Zarghi
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引用次数: 0

摘要

乳腺癌是一种侵袭性疾病,在女性中发病率很高。尽管有各种各样的治疗方法,但研究仍在进行中,以找到治疗这种疾病的有效方法。本研究旨在合成一系列新的含氨基乙氧基侧链的二芳基苯并[d]咪唑[2,1-b]噻唑类化合物,并在体外研究其对人乳腺癌细胞株(MCF-7)的细胞毒性。用该支架合成了12个衍生物(6a-6l),并对其结构进行了光谱鉴定。衍生物对MCF-7细胞系的细胞毒性作用也用MTT法进行了评估。与他莫昔芬相比,这些化合物对MCF-7细胞株均有较好的抑制作用。化合物(6i)和(6j)表现出较高的细胞毒性,抑制作用分别为81%和73%。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Synthesis, Structural Characterization, and Cytotoxic Activity of New Benzo[d]imidazo[2,1-b]thiazole Derivatives Against MCF-7 Breast Cancer Cells.

Breast cancer is an invasive disease with a high prevalence among females. Despite various treatments, studies are still ongoing to find an effective treatment for this disease. This study aimed to synthesize a new series of diaryl benzo[d]imidazo[2,1-b]thiazole compounds containing aminoethoxy side chain and in vitro investigate their cytotoxicity on a human breast cancer cell line (MCF-7). Twelve derivatives (6a-6l) were synthesized from this scaffold, the structures of which were spectroscopically confirmed. The cytotoxic effects of the derivatives on the MCF-7 cell line were also assessed using the MTT assay. All these compounds showed a good inhibitory effect on the MCF-7 cell line, compared to that of tamoxifen. Compounds (6i) and (6j) showed higher cytotoxicity with relevant inhibitory effects of 81% and 73%, respectively.

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来源期刊
CiteScore
3.40
自引率
6.20%
发文量
52
审稿时长
2 months
期刊介绍: The Iranian Journal of Pharmaceutical Research (IJPR) is a peer-reviewed multi-disciplinary pharmaceutical publication, scheduled to appear quarterly and serve as a means for scientific information exchange in the international pharmaceutical forum. Specific scientific topics of interest to the journal include, but are not limited to: pharmaceutics, industrial pharmacy, pharmacognosy, toxicology, medicinal chemistry, novel analytical methods for drug characterization, computational and modeling approaches to drug design, bio-medical experience, clinical investigation, rational drug prescribing, pharmacoeconomics, biotechnology, nanotechnology, biopharmaceutics and physical pharmacy.
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