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三萜皂苷 A-D:从蒺藜科植物蒺藜的枝叶中分离得到的四个未描述的甾体糖苷及其对 LPS 激活的 RAW 264.7 细胞中 NO 生成的抑制活性。

Tributelosides A-D: Four Undescribed Spirostan Glycosides Isolated from the Branches and Leaves of Tribulus terrestris with Their NO Production Inhibitory Activity in LPS Activated RAW 264.7 Cells.

机构信息

School of chemistry, biology and environment, Vinh University, 182 Le Duan, Ben Thuy, Vinh City, Nghe An, 461010, Vietnam.

Institute of Marine Biochemistry, VAST, 18 Hoang Quoc Viet, Cau Giay, Hanoi, 10072, Vietnam.

出版信息

Chem Biodivers. 2024 Aug;21(8):e202401049. doi: 10.1002/cbdv.202401049. Epub 2024 Jun 25.

Abstract

Four undescribed spirostan glycosides, (25S)-5α-spirostan- 12-one-2α,3β-diol-3-O-β-D-glucopyranosyl-(1→4)-β-D-galactopyranoside (1), (25S)-5α-spirostan-12-one-2α,3β-diol-3-O-β-D-galatopyranosyl-(1→2)-β-D-glucopyranosyl- (1→4)-β-D-galactopyranoside (2), (25S)-5α-spirostan-12-one-2α,3β-diol-3-O-β-D-glucopyranosyl-(1→2)-[β-D-glucopyranosyl-(1→3)]-β-D-glucopyranosyl-(1→4)-β-D-galactopyranoside (3), and hecogenin 3-O-β-D-glucopyranosyl-(1→3)-[β-D-xylopyranosyl-(1→2)]-β-D-glucopyranosyl-(1→4)-[α-L-rhamnopyranosyl-(1→2)]-β-D-galactopyranoside (4), together with eleven known compounds (5-15) were isolated from the branches and leaves of Tribulus terrestris. Their chemical structures were established through spectroscopic methods, including HR-ESI-MS, 1D-, and 2D-NMR spectra. Preliminary biological evaluation on NO production inhibitory activity in LPS activated RAW 264.7 cells showed that compounds 1-3, 5, and 6 had significant inhibitory effects with IC values ranging from 2.4 to 18.3 μM, compared to that of the positive control compound, dexamethazone (IC 13.6 μM).

摘要

从蒺藜科植物蒺藜的枝叶中分离得到四个未知甾体糖苷化合物,分别为(25S)-5α-螺旋甾烷-12-酮-2α,3β-二醇-3-O-β-D-吡喃葡萄糖基-(1→4)-β-D-吡喃半乳糖苷(1)、(25S)-5α-螺旋甾烷-12-酮-2α,3β-二醇-3-O-β-D-吡喃半乳糖基-(1→2)-β-D-吡喃葡萄糖基-(1→4)-β-D-吡喃半乳糖苷(2)、(25S)-5α-螺旋甾烷-12-酮-2α,3β-二醇-3-O-β-D-吡喃葡萄糖基-(1→2)-[β-D-吡喃葡萄糖基-(1→3)]-β-D-吡喃葡萄糖基-(1→4)-β-D-吡喃半乳糖苷(3)和戟生醇 3-O-β-D-吡喃葡萄糖基-(1→3)-[β-D-木糖基-(1→2)]-β-D-吡喃葡萄糖基-(1→4)-[α-L-鼠李糖基-(1→2)]-β-D-吡喃半乳糖苷(4),以及 11 个已知化合物(5-15)。通过 HR-ESI-MS、1D 和 2D-NMR 光谱等光谱方法确定了它们的化学结构。初步的生物评价结果表明,化合物 1-3、5 和 6 在 LPS 激活的 RAW 264.7 细胞中对 NO 产生的抑制活性具有显著的抑制作用,IC 值范围为 2.4-18.3 μM,与阳性对照化合物地塞米松(IC 13.6 μM)相比。

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