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来自波斯蒿的11种未描述的没药烷型倍半萜类化合物。

Eleven undescribed bisabolane-type sesquiterpenoids from Artemisia persica.

作者信息

Umaraliev Jakhongir, Ganiev Adkham, Turak Ablajan, Begmatov Nurmirza, Bobakulov Khayrulla, Abdullaev Nasrulla, Jiangyu Zhao, Aisa Haji Akber

机构信息

State Key Laboratory Basis of Xinjiang Indigenous Medicinal Plants Resource Utilization and the Key Laboratory of Plant Resources and Chemistry of Arid Zone, Xinjiang Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Urumqi, 830011, China; University of Chinese Academy of Sciences, Beijing, 100049, China.

Acad. S. Yu. Yunusov Institute of the Chemistry of Plant Substances, Academy of Sciences of the Republic of Uzbekistan, 77, M. Ulugbek str., 100170, Tashkent, Uzbekistan.

出版信息

Phytochemistry. 2025 Nov;239:114602. doi: 10.1016/j.phytochem.2025.114602. Epub 2025 Jun 27.

Abstract

Eleven previously undescribed bisabolane-type sesquiterpenoids were successfully isolated from Artemisia persica. The structures of these compounds were comprehensively elucidated through a combination of advanced spectroscopic techniques, including one-dimensional and two-dimensional nuclear magnetic resonance, high-resolution electrospray ionization mass spectrometry, and ultraviolet spectroscopy. Structural assignments were further confirmed by comparison of experimental and time-dependent density functional theory-calculated electronic circular dichroism spectra, as well as single-crystal X-ray diffraction analysis where applicable. To assess their pharmacological relevance, the isolated sesquiterpenoids were subjected to in vitro evaluation of anti-inflammatory activity and cytotoxic potential. Compounds 6 and 9 demonstrated limited anti-inflammatory activity in the lipopolysaccharide-induced inflammation model using RAW 264.7 mouse macrophages, with IC values of 111.1 ± 4.66 μM and 247.8 ± 1.49 μM, respectively.

摘要

从波斯蒿中成功分离出11种此前未被描述的没药烷型倍半萜类化合物。通过结合先进的光谱技术,包括一维和二维核磁共振、高分辨率电喷雾电离质谱和紫外光谱,对这些化合物的结构进行了全面阐释。通过比较实验和含时密度泛函理论计算的电子圆二色光谱,以及在适用情况下的单晶X射线衍射分析,进一步证实了结构归属。为了评估它们的药理相关性,对分离得到的倍半萜类化合物进行了抗炎活性和细胞毒性潜力的体外评估。在使用RAW 264.7小鼠巨噬细胞的脂多糖诱导炎症模型中,化合物6和9表现出有限的抗炎活性,IC值分别为111.1±4.66μM和247.8±1.49μM。

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