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白花蛇舌草中的单萜-黄酮苷及其自噬调节活性。

Monoterpene-flavonoid conjugates from Sarcandra glabra and their autophagy modulating activities.

机构信息

State Key Laboratory of Quality Research in Chinese Medicine, Guangdong-Hong Kong-Macao Joint Laboratory of Respiratory Infectious Disease, Macau Institute for Applied Research in Medicine and Health, Macau University of Science and Technology, Macau; Biology Institute, Qilu University of Technology (Shandong Academy of Sciences), Jinan 250103, People's Republic of China.

State Key Laboratory of Quality Research in Chinese Medicine, Guangdong-Hong Kong-Macao Joint Laboratory of Respiratory Infectious Disease, Macau Institute for Applied Research in Medicine and Health, Macau University of Science and Technology, Macau.

出版信息

Bioorg Chem. 2021 Jul;112:104830. doi: 10.1016/j.bioorg.2021.104830. Epub 2021 Mar 18.

Abstract

Fourteen new monoterpene-flavonoid conjugates including four monoterpene-conjugated chalcones (glabratins A-D, 1-4), seven monoterpene-conjugated dihydrochalcones (glabratins E-K, 5-11), and three monoterpene-conjugated flavanones (glabratins L-N, 12-14), together with four known analogues (15-18) were isolated from the aerial parts of Sarcandra glabra. The structures and the absolute configurations of these compounds were elucidated by the spectroscopic data, single-crystal X-ray diffraction, and electronic circular dichroism (ECD) calculations. Compounds 1, 4-6, 9-14, and 18 showed obvious cell autophagy-inducing activities at 25 μM in HEK293 cells. Furthermore, the bioassay results also showed that 18 induced cell autophagy in a dose dependent manner. Our findings revealed a rare class of monoterpene-flavonoid conjugates in nature and firstly reported their autophagy-inducing activities.

摘要

从白花蛇舌草的地上部分分离得到 14 个新的单萜类黄酮类化合物,包括 4 个单萜类共轭查尔酮(格拉巴汀 A-D,1-4)、7 个单萜类共轭二氢查尔酮(格拉巴汀 E-K,5-11)和 3 个单萜类共轭黄烷酮(格拉巴汀 L-N,12-14),以及 4 个已知类似物(15-18)。这些化合物的结构和绝对构型通过光谱数据、单晶 X 射线衍射和电子圆二色性(ECD)计算来阐明。在 HEK293 细胞中,化合物 1、4-6、9-14 和 18 在 25μM 时表现出明显的细胞自噬诱导活性。此外,生物测定结果还表明 18 以剂量依赖的方式诱导细胞自噬。我们的发现揭示了自然界中一类罕见的单萜类黄酮类化合物,并首次报道了它们的自噬诱导活性。

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