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苦参中的喹诺里西啶生物碱具有抗炎和抗肿瘤特性。

Quinolizidine alkaloids from Sophora alopecuroides with anti-inflammatory and anti-tumor properties.

机构信息

Faculty of Life Science and Technology, Kunming University of Science and Technology, Kunming 650500, Yunnan, PR China.

Faculty of Life Science and Technology, Kunming University of Science and Technology, Kunming 650500, Yunnan, PR China.

出版信息

Bioorg Chem. 2021 May;110:104781. doi: 10.1016/j.bioorg.2021.104781. Epub 2021 Feb 27.

Abstract

Forty-three quinolizidine alkaloids (1-43), including twelve new matrine-type ones, sophalodes A-L (1-7, 17, 19 and 28-30), were isolated from the seeds of Sophora alopecuroides. Structurally, compounds 1-4 were the first examples of C-11 oxidized matrine-type alkaloids from Sophora plants. The structures and absolute configurations of new compounds were elucidated by extensive spectroscopic techniques, X-ray diffraction analysis, and quantum chemical calculation. In addition, the NMR data and absolute configuration of compound 18 was reported for the first time. All the isolates were evaluated for their inhibition on nitric oxide production induced by lipopolysaccharide in RAW 264.7 macrophages, among them, compounds 29, 38 and 42 exhibited the most significant activity with IC values of 29.19, 25.86 and 33.30 μM, respectively. Further research about new compound 29 showed that it also suppressed the protein levels of iNOS and COX-2, which revealed its anti-inflammatory potential. Moreover, additional research showed that compound 16 exhibited marginal cytotoxicity against HeLa cell lines, with an IC value of 24.27 μM.

摘要

从苦参种子中分离得到了 43 种喹诺里西啶生物碱(1-43),包括 12 种新的苦参碱型生物碱 sophalodes A-L(1-7、17、19 和 28-30)。结构上,化合物 1-4 是从苦参属植物中分离得到的首例 C-11 氧化苦参碱型生物碱。新化合物的结构和绝对构型通过广泛的光谱技术、X 射线衍射分析和量子化学计算确定。此外,18 号化合物的 NMR 数据和绝对构型也是首次报道。对所有分离得到的化合物进行了抑制脂多糖诱导 RAW 264.7 巨噬细胞一氧化氮产生的活性评价,其中,化合物 29、38 和 42 的抑制活性最强,IC50 值分别为 29.19、25.86 和 33.30 μM。对新化合物 29 的进一步研究表明,它还抑制了 iNOS 和 COX-2 的蛋白水平,显示出其抗炎潜力。此外,进一步的研究表明,化合物 16 对 HeLa 细胞系表现出一定的细胞毒性,IC50 值为 24.27 μM。

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