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来自小果阿福花的生物活性次级代谢产物。

Biologically active secondary metabolites from Asphodelus microcarpus.

作者信息

Ghoneim Mohammed M, Ma Guoyi, El-Hela Atef A, Mohammad Abd-Elsalam I, Kottob Saeid, El-Ghaly Sayed, Cutler Stephen J, Ross Samir A

机构信息

National Center for Natural Products Research School of Pharmacy, The University of Mississippi, University, MS 38677, USA.

出版信息

Nat Prod Commun. 2013 Aug;8(8):1117-9.

Abstract

Bioassay guided fractionation of the ethanolic extract of Asphodelus microcarpus Salzm.et Vivi (Asphodelaceae) resulted in the isolation of one new metabolite, 1,6-dimethoxy-3-methyl-2-naphthoic acid (1) as well as nine known compounds: asphodelin (2), chrysophanol (3), 8-methoxychrysophanol (4), emodin (5), 2-acetyl-1,8-dimethoxy-3-methylnaphthalene (6), 10-(chrysophanol-7'-yl)-10-hydroxychrysophanol-9-anthrone (7), aloesaponol-III-8-methyl ether (8), ramosin (9) and aestivin (10). The compounds were identified by 1D and 2D NMR and HRESIMS. Compounds 3, 6 and 10 were isolated for the first time from this species. Compounds 3 and 4 showed moderate to weak antileishmanial activity with IC50 values of 14.3 and 35.1 microg/mL, respectively. Compound 4 exhibited moderate antifungal activity against Cryptococcus neoformans with an IC50 value of 15.0 microg/mL, while compounds 5, 7 and 10 showed good to potent activity against methicillin resistant Staphylococcus aureus (MRSA) with IC50 values of 6.6, 9.4 microg/mL and 1.4 microg/mL respectively. Compounds 5, 8 and 9 displayed good activity against S. aureus with IC50 values of 3.2, 7.3 and 8.5 microg/mL, respectively. Compounds 7 and 9 exhibited a potent cytotoxic activity against leukemia LH60 and K562 cell lines. Compound 10 showed potent antimalarial activities against both chloroquine-sensitive and chloroquine-resistant strains of Plasmodium falciparum with IC50 values in the range of 0.8-0.7 microg/mL without showing any cytotoxicity to mammalian cells.

摘要

对小果阿福花(Asphodelus microcarpus Salzm.et Vivi,阿福花科)乙醇提取物进行生物测定导向的分离,得到一种新的代谢产物1,6 - 二甲氧基 - 3 - 甲基 - 2 - 萘甲酸(1)以及九种已知化合物:阿福花苷(2)、大黄酚(3)、8 - 甲氧基大黄酚(4)、大黄素(5)、2 - 乙酰基 - 1,8 - 二甲氧基 - 3 - 甲基萘(6)、10 - (大黄酚 - 7'- 基) - 10 - 羟基大黄酚 - 9 - 蒽酮(7)、芦荟皂醇 - III - 8 - 甲醚(8)、拉莫辛(9)和夏眠素(10)。这些化合物通过一维和二维核磁共振以及高分辨电喷雾电离质谱进行鉴定。化合物3、6和10首次从该物种中分离得到。化合物3和4表现出中度至弱的抗利什曼原虫活性,IC50值分别为14.3和35.1微克/毫升。化合物4对新型隐球菌表现出中度抗真菌活性,IC50值为15.0微克/毫升,而化合物5、7和10对耐甲氧西林金黄色葡萄球菌(MRSA)表现出良好至强效活性,IC50值分别为6.6、9.4微克/毫升和1.4微克/毫升。化合物5、8和9对金黄色葡萄球菌表现出良好活性,IC50值分别为3.2、7.3和8.5微克/毫升。化合物7和9对白血病LH60和K562细胞系表现出强效细胞毒性活性。化合物10对氯喹敏感和氯喹耐药的恶性疟原虫菌株均表现出强效抗疟活性,IC50值在0.8 - 0.7微克/毫升范围内,且对哺乳动物细胞无任何细胞毒性。

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