
基本信息:
- 专利标题: 一种生物碱类化合物及其制备方法与作为抗单纯疱疹Ⅰ型病毒剂的应用
- 专利标题(英):Alkaloid compound, preparation method thereof and application as anti-herpes simplex virus I agent
- 申请号:CN201510918196.7 申请日:2015-12-14
- 公开(公告)号:CN106496202A 公开(公告)日:2017-03-15
- 发明人: 邵长伦 , 王长云 , 牟晓凤 , 胥汝芳
- 申请人: 中国海洋大学
- 申请人地址: 山东省青岛市崂山区松岭路238号中国海洋大学
- 专利权人: 中国海洋大学
- 当前专利权人: 中国海洋大学
- 当前专利权人地址: 山东省青岛市崂山区松岭路238号中国海洋大学
- 优先权: 201510561145.3 2015.09.06 CN
- 生物保藏信息: CGMCC 6959 2012.12.17
- 主分类号: C07D405/06
- IPC分类号: C07D405/06 ; C07D215/22 ; C12P17/12 ; C12P17/16 ; A61K31/4704 ; A61K31/4709 ; A61P31/22
The invention relates to an alkaloid compound, a preparation method thereof and application as an anti-herpes simplex virus I agent. The preparation method includes: firstly conducting strain fermentation culture on fungus Scopulariopsis sp. (TA01-33), extracting and concentrating fermentation broth, then carrying out normal phase silica gel column chromatography, SephadexLH-20 gel column chromatography, and HPLC (high performance liquid chromatography) in order to obtain a formula I compound, and carrying out a series of conventional chemical reactions on the formula I compound, thus obtaining compounds shown as formula II-formula V. The invention provides the anti-herpes simplex virus I agent, and the formula I-formula V compounds or provided by the invention or the pharmaceutically acceptable salts thereof can be used for treating diseases caused by herpes simplex virus I.
公开/授权文献:
- CN106496202B 一种生物碱类化合物及其制备方法与作为抗单纯疱疹Ⅰ型病毒剂的应用 公开/授权日:2019-08-06
IPC结构图谱:
C | 化学;冶金 |
--C07 | 有机化学 |
----C07D | 杂环化合物 |
------C07D405/00 | 杂环化合物,含有1个或多个以氧原子作为仅有的杂环原子的环,且含有1个或多个以氮原子作为仅有的杂环原子的环 |
--------C07D405/02 | .含有两个杂环 |
----------C07D405/06 | ..被仅含脂族碳原子的碳链连接的 |