Foegraecumoside O and P, a Pair of Triterpenoid Saponins with a 4/5/6 Fused Tricyclic Oleanane Carbon Skeleton from Lysimachia foenum-graecum Hance

被引:1
|
作者
Dai, Lumei [1 ,2 ]
He, Shuang [1 ]
Zhang, Bin [1 ]
Wang, Hengshan [1 ]
Wang, Yan [1 ,3 ]
Liang, Dong [1 ]
机构
[1] Guangxi Normal Univ, Sch Chem & Pharmaceut Sci, State Key Lab Chem & Mol Engn Med Resources, Guilin 541004, Peoples R China
[2] Huanghuai Univ, Sch Biol & Food Engn, Zhumadian 463000, Peoples R China
[3] Univ Karachi, H E J Res Inst Chem, Int Ctr Chem & Biol Sci, Karachi 75270, Pakistan
来源
MOLECULES | 2023年 / 28卷 / 13期
基金
中国国家自然科学基金;
关键词
Primulaceae; Lysimachia; Lysimachia foenum-graecum; triterpenoids; cytotoxicity; DRUG-RESISTANCE; CANCER;
D O I
10.3390/molecules28135061
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Lysimachia foenum-graecum Hance (Primulaceae) is a medicinal plant used for cold, pain, ascariasis, etc., in China. Triterpenoid saponins have been found to be the main components of this genus. In this work, a pair of oleanane-type triterpenoid saponins with an unprecedented 4/5/6 fused tricyclic skeleton, foegraecumoside O (1) and foegraecumoside P (2) were isolated from the butanol fraction of the aerial parts of L. foenum-graecum. Their structures were determined using chemical methods and extensive spectroscopic analyses, along with quantum chemical calculations. Compound 2 displayed moderate cytotoxicity against HepG2, MGC-803, T24, NCI-H460, A549, and A549/CDDP (drug-resistant lung-cancer cell line) with IC50 at 12.4-19.2 & mu;M in an MTT assay, comparing with the positive control doxorubicin, which had IC50 at 0.53-4.92 & mu;M, but was inactive for A549/CDDP. Furthermore, a possible biosynthetic pathway for forming compounds 1 and 2 was proposed.
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页数:12
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