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对具有泻下活性的墨西哥药喇叭根树脂糖苷含量进行分析。

Profiling of the resin glycoside content of Mexican jalap roots with purgative activity.

作者信息

Pereda-Miranda Rogelio, Fragoso-Serrano Mabel, Escalante-Sanchez Edgar, Hernandez-Carlos Beatriz, Linares Edelmira, Bye Robert

机构信息

Departamento de Farmacia, Facultad de Química, Universidad Nacional Autónoma de México, Ciudad Universitaria, Mexico City 04510 DF, Mexico.

出版信息

J Nat Prod. 2006 Oct;69(10):1460-6. doi: 10.1021/np060295f.

Abstract

Mexican Jalap roots, a prehispanic medicinal plant complex still considered to be a useful laxative, can be found as an ingredient in some over-the-counter products sold by herbalists in contemporary Mexico. The drug is prepared from the dried roots of several morning glories, all of which have been identified as members of the genus Ipomoea. Analysis of several commercial samples was assessed by generating HPLC and 13C NMR spectroscopic profiles of the glycosidic acids obtained through saponification of the resin glycoside contents. These profiles distinguish the three Mexican jalaps currently in frequent use and can serve as analytical tools for the authentication and quality control of these purgative herbal drugs. Ipomoea purga, the authentic "jalap root", yielded two new hexasaccharides of convolvulinic and jalapinolic acids, purgic acids A (1) and B (2), respectively. Scammonic acid A (3), a tetrasaccharide, was produced from Ipomoea orizabensis, the Mexican scammony or false jalap. Operculinic acid B (4), a pentasaccharide, was identified in Ipomoea stans. Semipreparative HPLC was performed to obtain pure samples of new compounds 1 and 2 in sufficient quantity to elucidate their structure by high-field NMR spectroscopy. Purgic acid A (1) was identified as (11S)-hydroxytetradecanoic acid 11-O-beta-D-quinovopyranosyl-(1-->2)-O-beta-D-glucopyranosyl-(1-->3)-O-[beta-D-fucopyranosyl-(1-->4)]-O-alpha-L-rhamnopyranosyl-(1-->2)-O-beta-D-glucopyranosyl-(1-->2)-O-beta-D-quinovopyranoside, while purgic acid B (2) was characterized with (11S)-hydroxyhexadecanoic acid as its aglycon but having the same glycosidation sequence in the oligosaccharide core.

摘要

墨西哥药喇叭根是一种前西班牙时期的药用植物复合体,至今仍被视为一种有效的泻药,在当代墨西哥的草药商所售的一些非处方产品中可作为一种成分找到。这种药物由几种旋花科植物的干燥根制成,所有这些植物均已被鉴定为甘薯属成员。通过对树脂糖苷成分皂化得到的糖苷酸生成高效液相色谱(HPLC)和13C核磁共振(NMR)光谱图,对几种商业样品进行了分析评估。这些图谱区分了目前常用的三种墨西哥药喇叭,可作为这些泻药草药鉴定和质量控制的分析工具。正宗的“药喇叭根”—— 紫茉莉,分别产生了两种新的旋花酸和药喇叭酸己糖,即药喇叭酸A(1)和B(2)。四糖斯卡蒙酸A(3)由墨西哥司格蒙旋花或假药喇叭 —— 奥里萨巴甘薯产生。在斯坦氏甘薯中鉴定出了五糖盖裂果酸B(4)。进行了半制备HPLC以获得足够量的新化合物1和2的纯样品,以便通过高场NMR光谱阐明其结构。药喇叭酸A(1)被鉴定为(11S)-羟基十四烷酸11-O-β-D-奎诺吡喃糖基-(1→2)-O-β-D-吡喃葡萄糖基-(1→3)-O-[β-D-岩藻吡喃糖基-(1→4)]-O-α-L-鼠李吡喃糖基-(1→2)-O-β-D-吡喃葡萄糖基-(1→2)-O-β-D-奎诺吡喃糖苷,而药喇叭酸B(2)的特征是以(11S)-羟基十六烷酸为其苷元,但在寡糖核心中具有相同的糖苷化序列。

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