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来自菊叶山萝卜的生物活性三萜类化合物。

Biologically active triterpenoids from Cephalaria ambrosioides.

作者信息

Pasi Sofia, Aligiannis Nektarios, Pratsinis Harris, Skaltsounis Alexios-Leandros, Chinou Ioanna B

机构信息

Department of Pharmacognosy and Natural Products Chemistry, School of Pharmacy, University of Athens, Athens, Greece.

出版信息

Planta Med. 2009 Feb;75(2):163-7. doi: 10.1055/s-0028-1088391. Epub 2009 Jan 16.

Abstract

The roots of Cephalaria ambrosioides yielded a new triterpene, 6alpha-hydroxyhederagenic acid ( 1), in addition to the known triterpene hederagenic acid ( 2) and four corresponding saponins, leontoside A (or akeboside Stb) ( 3), kalopanax saponin A (or alpha-hederin) ( 4), saponin PG (or sapindoside B) ( 5), and dipsacoside B ( 6). Their structures have been elucidated on the basis of their spectral data (MS, 1 D and 2 D NMR) and by some chemical transformations. The extract and all isolated compounds were evaluated for their antimicrobial, molluscicidal and IN VITRO cytotoxic activities. All compounds showed strong antimicrobial activity (MIC values 1.80 - 2.50 microg/mL), with 5 and 6 exhibiting activities comparable to those of standard antibiotics. Moreover, compounds 3 - 5 were active against all assayed cancer cell lines, whereas compounds 3 and 4 exhibited higher activities against Biomphalaria Glabrata snails, with minimum inhibitory concentrations of 5.4 and 6.2 microg/mL, respectively.

摘要

除了已知的三萜类化合物常春藤皂苷元(2)和四种相应的皂苷,即狮牙草苷A(或木通皂苷Stb)(3)、刺五加皂苷A(或α-常春藤皂苷)(4)、皂苷PG(或无患子皂苷B)(5)和川续断皂苷B(6)之外,滇川风铃草(Cephalaria ambrosioides)的根还产生了一种新的三萜类化合物,6α-羟基常春藤皂苷元(1)。它们的结构已通过光谱数据(质谱、一维和二维核磁共振)以及一些化学转化得以阐明。对提取物和所有分离出的化合物进行了抗菌、杀螺和体外细胞毒性活性评估。所有化合物均表现出较强的抗菌活性(最低抑菌浓度值为1.80 - 2.50微克/毫升),其中化合物5和6的活性与标准抗生素相当。此外,化合物3 - 5对所有检测的癌细胞系均有活性,而化合物3和4对光滑双脐螺表现出更高的活性,最低抑菌浓度分别为5.4和6.2微克/毫升。

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