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新型螺-4-吡喃衍生物的抗菌活性、细胞毒性及促凋亡作用的合成与评价

Synthesis and evaluation of antimicrobial activity, cytotoxic and pro-apoptotic effects of novel spiro-4-pyran derivatives.

作者信息

Safari Fatemeh, Hosseini Hajar, Bayat Mohammad, Ranjbar Ashkan

机构信息

Department of Biology, Faculty of Science, University of Guilan Rasht Iran

Department of Chemistry, Faculty of Science, Imam Khomeini International University Qazvin Iran

出版信息

RSC Adv. 2019 Aug 9;9(43):24843-24851. doi: 10.1039/c9ra03196k. eCollection 2019 Aug 8.

Abstract

A new library of spiropyrans were synthesized a one-pot four component reaction of cyanoacetohydrazide, ninhydrin, malononitrile and various cyclic CH-acids in EtOH at reflux conditions. The products were isolated and tested for antibacterial effects on () and (). Furthermore cytotoxic activity of the spiropyrans on non-small-cell lung cancer cells (A549 cells), a breast epithelial cancer cell line (MCF-7), human malignant melanoma cells (A375), prostate cancer cells (PC3 cells, LNCaP cells) and normal cells HDF (human dermal fibroblast) was investigated. Interestingly, it was found that compounds 5a, 5b, 5f, 5g and 5i have the best MIC against and compound 5a displayed the most potent activity against A549, A375, and LNCaP tumor cells. Moreover, DAPI staining of the A549 cancer cell lines that were treated with 5a were associated with the death of A549 cells. By using RT-PCR method, it was finally confirmed that apoptosis occurs in A549 cells by up-regulated Bax expression and down-regulated Bcl-2 expression from the mitochondrial pathway of apoptosis.

摘要

通过氰基乙酰肼、茚三酮、丙二腈和各种环状CH-酸在乙醇中回流条件下的一锅四组分反应,合成了一个新的螺吡喃文库。分离出产物并测试其对()和()的抗菌作用。此外,还研究了螺吡喃对非小细胞肺癌细胞(A549细胞)、乳腺上皮癌细胞系(MCF-7)、人恶性黑色素瘤细胞(A375)、前列腺癌细胞(PC3细胞、LNCaP细胞)和正常细胞HDF(人皮肤成纤维细胞)的细胞毒性活性。有趣的是,发现化合物5a、5b、5f、5g和5i对()具有最佳的最低抑菌浓度,化合物5a对A549、A375和LNCaP肿瘤细胞表现出最有效的活性。此外,用5a处理的A549癌细胞系的DAPI染色与A549细胞的死亡有关。通过使用RT-PCR方法,最终证实A549细胞通过凋亡线粒体途径中Bax表达上调和Bcl-2表达下调而发生凋亡。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c78/9070039/47bfb4fbfdd5/c9ra03196k-s1.jpg

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