首页> 外文学位 >Identification of Acetylcholinesterase Inhibiting Natural Products From Buxus natalensis and Drypetes gossweileri.
【24h】

Identification of Acetylcholinesterase Inhibiting Natural Products From Buxus natalensis and Drypetes gossweileri.

机译:鉴定乙酰胆碱酯酶抑制天然黄杨和百里香干燥产物的天然产物。

获取原文
获取原文并翻译 | 示例

摘要

This thesis describes phytochemical studies on two medically important plants, Buxus natalensis and Drypetes gossweileri .;Phytochemical studies on the crude extract of Drypetes gossweileri resulted in the isolation of a new N-linked aromatic glycoside, N-beta-glucopyranosyl-p-hydroxy phenyl acetamide (151), along with two known compounds, p-hydroxy phenyl acetic acid (152) and p-hydroxyphenyl acetonitrile (153). Compounds 151-153 exhibited moderate to weak AChE inhibitory activities.;Chemical investigation on the acetylcholinesterase inhibiting chloroform extracts, obtained at pH 7.0 and 9.5 resulted in the isolation of seven natural products: O10-natafuranamine (123), cyclonataminol A (124), 31-demethylbuxaminol A (125), buxaminol A (126), buxaminol C (127), p -coumaroylputrescine (128) and methyl syringate ( 129). Compound 123 is a member of a rarely occurring class of Buxus alkaloids containing a tetrahydrofuran ring incorporated in its structure. Compounds 123-129 were isolated for the first time from this plant. Structures of compounds 123-129 were elucidated with the aid of NMR and MS spectral data. All of these isolates exhibited different levels of AChE inhibitory activities with compound 123 being significantly active in this bioassay with an IC50 of 8.5 microM compared to the rest of the isolates. Compounds 123-129 were inactive in antimicrobial assays.
机译:本论文描述了对两种医学上重要的植物,Buxus natalensis和Drypetes gossweileri的植物化学研究;对Drypetes gossweileri粗提物的植物化学研究导致分离出一种新的N-连接的芳香族糖苷,N-β-吡喃葡萄糖基-对羟基苯基乙酰胺(151),以及两种已知化合物对羟基苯乙酸(152)和对羟基苯基乙腈(153)。化合物151-153表现出中等至弱的AChE抑制活性。对pH 7.0和9.5的乙酰胆碱酯酶抑制性氯仿提取物的​​化学研究导致分离出7种天然产物:O10-那呋喃胺(123),环己胺A(124), 31-脱甲基丁氨醇A(125),丁氨醇A(126),丁氨醇C(127),对-香豆酰putrescine(128)和丁香酸甲酯(129)。化合物123是在其结构中结合有四氢呋喃环的很少发生的黄雀生物碱类的成员。首次从该植物中分离出化合物123-129。借助NMR和MS光谱数据阐明了化合物123-129的结构。所有这些分离物均表现出不同水平的AChE抑制活性,与其他分离物相比,化合物123在该生物测定中具有显着活性,IC50为8.5 microM。化合物123-129在抗菌测定中没有活性。

著录项

  • 作者单位

    University of Manitoba (Canada).;

  • 授予单位 University of Manitoba (Canada).;
  • 学科 Chemistry Organic.
  • 学位 M.Sc.
  • 年度 2010
  • 页码 198 p.
  • 总页数 198
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号