Secondary metabolites from Detarium microcarpum Guill. and Perr. (Fabaceae).

IF 2.1 Zeitschrift fur Naturforschung. C, Journal of biosciences Pub Date : 2022-02-23 Print Date: 2022-05-25 DOI:10.1515/znc-2021-0239
William Fouatio Feudjou, Arnaud Michel Mbock, Valerie Tedjon Sielinou, Hugue Fouotsa, Steven Collins Njonté Wouamba, Racéline Kamkumo Gounoue, Marcel Freeze, Hans-Georg Stammler, Jean Jules Kezeutas Bankeu, Mkounga Pierre, Bruno Ndjakou Lenta, Alembert Tiabou Tchinda, Norbert Sewald, Augustin Ephrem Nkengfack
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引用次数: 2

Abstract

The chemical investigation of the ethanol/water (7:3) extract of the roots of Detarium microcarpum (Fabaceae) led to the isolation of one new labdane diterpenoid, microcarpin (1) and one new ceramide derivative, microcarpamide (2), along with eight known secondary metabolites (3-10) including, 5-(carboxymethyl)-5,6,8a-trimethyl-3,4,4a,5,6,7,8,8a-octahydronaphthalene-1-carboxylic acid (3), microcarposide (4), rhinocerotinoic acid (5), 1,7-dihydroxy-6-methylxanthone (6), ursolic acid (7), 3β,23-dihydroxylup-20(29)-en-28-oic acid (8), alphitolic acid (9), and stigmasterol glucoside (10). The structures of these compounds were elucidated based on their spectroscopic data. Although compounds 3 and 4 are known, their crystalline structures are reported here for the first time. These compounds were evaluated in vitro for their antisalmonella activity. The results obtained showed that, microcarpamide (2), microcarposide (4), and rhinocerotinoic acid (5) were moderately active against three salmonella strains: Salmonella typhi, Salmonella enteritidis and Salmonella typhimirium, with minimum inhibition concentration values of 76.7 and 153.5 μM.

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来自小果苣苔的次生代谢物。和佩尔。(蚕豆科)。
通过对Fabaceae植物Detarium microcarpum根乙醇/水(7:3)提取物的化学研究,分离出一种新的labdane二萜类化合物microcarpin(1)和一种新的神经酰胺衍生物microcarpamide(2),以及8种已知的次生代谢产物(3-10),包括5-(羧甲基)-5,6,8a-三甲基-3,4,4a,5,6,7,8,8a-八氢萘-1-羧酸(3),microcarposide (4), rhinocerotinoic酸(5),1,7-二羟基-6-甲基山酮(6),熊果酸(7),3β,23-二羟基-20(29)-烯-28-酸(8),α -酚酸(9)和豆甾醇糖苷(10)。根据光谱数据对这些化合物的结构进行了分析。虽然化合物3和4是已知的,但它们的晶体结构在这里是首次报道。对这些化合物的体外抗沙门氏菌活性进行了评价。结果表明,微卡帕胺(2)、微卡帕苷(4)和鼻角酸(5)对伤寒沙门菌、肠炎沙门菌和鼠伤寒沙门菌3株沙门菌均有中等活性,最小抑制浓度分别为76.7 μM和153.5 μM。
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