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从美丽紫珠中分离和鉴定 3,4-裂环劳丹烷二萜类化合物及其对 HepG2 细胞的细胞毒性研究。

Isolation and identification of 3,4-seco-labdane diterpenoids from Callicarpa nudiflora and investigation of their cytotoxicity against HepG2 cells.

机构信息

Key Laboratory of Standardization of Chinese Medicines, Ministry of Education, Institute of Chinese Materia Medica of Shanghai University of Traditional Chinese Medicine, Cai Lun Road 1200, Zhangjiang, Shanghai, 201203, PR China.

Key Laboratory of Standardization of Chinese Medicines, Ministry of Education, Institute of Chinese Materia Medica of Shanghai University of Traditional Chinese Medicine, Cai Lun Road 1200, Zhangjiang, Shanghai, 201203, PR China; Shanghai R&D Center for Standardization of Chinese Medicines, Cai Lun Road 1200, Zhangjiang, Shanghai, 201203, PR China.

出版信息

Phytochemistry. 2023 Sep;213:113773. doi: 10.1016/j.phytochem.2023.113773. Epub 2023 Jun 28.

Abstract

Twenty-one previously undescribed compounds, including nineteen 3,4-seco-labdanes (nudiflopenes P-W, Y, A-J), one 3,4-seco-pimarane (nudiflopene X), and one labdane (nudiflopene Z), along with nine known compounds (one 3,4-seco-pimarane and eight 3,4-seco-labdanes) were isolated from the leaves of Callicarpa nudiflora Hook. Et Arn. The structures of these compounds were elucidated by high-resolution electrospray ionization mass spectrometry and one- and two-dimensional nuclear magnetic resonance spectroscopy. In addition, configurations of the isolated compounds were determined by electronic circular dichroism, DP4+ probability analysis, and single-crystal X-ray diffraction experiments. All undescribed compounds were evaluated for their cytotoxicity against HepG2 cells in vitro, among which compound 12 exhibited a moderate activity with an IC value of 27.8 μM.

摘要

从马银花(Callicarpa nudiflora Hook. Et Arn.)叶中分离得到 21 个从未被描述过的化合物,包括 19 个 3,4-裂环劳丹烷(nudiflopenes P-W、Y、A-J)、1 个 3,4-裂环松烷(nudiflopene X)和 1 个劳丹烷(nudiflopene Z),以及 9 个已知化合物(1 个 3,4-裂环松烷和 8 个 3,4-裂环劳丹烷)。这些化合物的结构通过高分辨电喷雾电离质谱和一维、二维核磁共振波谱得到了阐明。此外,通过电子圆二色性、DP4+ 概率分析和单晶 X 射线衍射实验确定了分离得到的化合物的构型。所有未被描述过的化合物都进行了体外细胞毒性评估,结果表明化合物 12 对 HepG2 细胞具有中等活性,IC 值为 27.8 μM。

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