Suppr超能文献

具有细胞周期阻滞和克服 TRAIL 耐药性活性的内生真菌多喙茎点霉 XJ-2-1 中的细胞松弛素。

Cytochalasins from an endophytic fungus Phoma multirostrata XJ-2-1 with cell cycle arrest and TRAIL-resistance-overcoming activities.

机构信息

School of Pharmacy, Tongji Medical College of Huazhong University of Science and Technology, Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, Wuhan 430030, People's Republic of China.

School of Pharmacy, Tongji Medical College of Huazhong University of Science and Technology, Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, Wuhan 430030, People's Republic of China.

出版信息

Bioorg Chem. 2020 Nov;104:104317. doi: 10.1016/j.bioorg.2020.104317. Epub 2020 Sep 25.

Abstract

Nine new (1-9) and four known (10-13) [13]cytochalasins, along with three known 24-oxa[14]cytochalasins (14-16), were isolated from the culture of Phoma multirostrata XJ-2-1, an endophytic fungus obtained from the fibrous root of Parasenecio albus. Their structures were elucidated by interpretation of the nuclear magnetic resonance (NMR) and high-resolution electrospray ionization mass spectroscopy (HRESIMS). The absolute configurations were assigned by single-crystal X-ray crystallography, modified Mosher's method, and by analysis of their experimental electronic circular dichroism (ECD) spectra. Compound 6 could induce cell cycle arrest at G2-phase in CT26 and A549 cells, and displayed moderate cytotoxicity against CT26 and A549 cell lines with IC values of 6.03 and 5.04 μM, respectively. Co-treatment of 7-9, 13 and 16 with tumor necrosis factor related apoptosis inducing ligand (TRAIL) could significantly decrease the cell viability of A549, which revealed that cytochalasins could possibly be a new group of TRAIL sensitizers in lung cancer therapy.

摘要

从内生真菌多毛孢(Phoma multirostrata) XJ-2-1 的培养物中分离得到了 9 个新的(1-9)和 4 个已知的(10-13)[13]细胞松弛素,以及 3 个已知的 24-氧代[14]细胞松弛素(14-16)。通过核磁共振(NMR)和高分辨率电喷雾电离质谱(HRESIMS)的解析,确定了它们的结构。通过单晶 X 射线晶体学、改进的 Mosher 法以及对其实验电子圆二色性(ECD)光谱的分析,确定了它们的绝对构型。化合物 6 可诱导 CT26 和 A549 细胞在 G2 期停滞,并对 CT26 和 A549 细胞系表现出中等的细胞毒性,IC 值分别为 6.03 和 5.04 μM。7-9、13 和 16 与肿瘤坏死因子相关凋亡诱导配体(TRAIL)共同处理可显著降低 A549 的细胞活力,这表明细胞松弛素可能是肺癌治疗中 TRAIL 增敏剂的一个新类别。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验