• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

从 子实体中分离得到的降三萜及其对 FAAH 的抑制活性。

Nor-triterpenoids from the fruiting bodies of and their inhibitory activity against FAAH.

机构信息

Department of Oncology, The Affiliated Zhongshan Hospital of Dalian University, Dalian, People's Republic of China.

College of Pharmacy, The First Affiliated Hospital of Dalian Medical University, Dalian, People's Republic of China.

出版信息

Nat Prod Res. 2023 Feb;37(4):579-585. doi: 10.1080/14786419.2022.2078817. Epub 2022 May 24.

DOI:10.1080/14786419.2022.2078817
PMID:35608196
Abstract

Two new nor-triterpenoids ganodrenol A (), B (), and a new natural product ganodrenol C (), along with three known nor-triterpenoids (-) were isolated from the fruiting bodies of The chemical structures of these isolates were determined by 1 D and 2 D NMR, HRESIMS, and X-ray crystallography analysis. The inhibitory effects of isolated triterpenoids (-) against FAAH were evaluated by an in assay, and compound showed an inhibition rate of 70.27%. In addition, the cytotoxic effect of compounds (-) was evaluated against LOVO, MCF-7, and RAW264.7 cells, which displayed no significant cytotoxicity.

摘要

从灵芝的子实体中分离得到了两个新的 nor-三萜醇 A ()、B () 和一个新的天然产物 ganodrenol C (),以及三个已知的 nor-三萜醇 (-)。通过 1D 和 2D NMR、HRESIMS 和 X 射线晶体学分析确定了这些分离物的化学结构。通过酶抑制测定法评估了分离得到的三萜醇 (-) 对 FAAH 的抑制作用,化合物 显示出 70.27%的抑制率。此外,还评估了化合物 (-) 对 LOVO、MCF-7 和 RAW264.7 细胞的细胞毒性作用,结果显示它们没有明显的细胞毒性。

相似文献

1
Nor-triterpenoids from the fruiting bodies of and their inhibitory activity against FAAH.从 子实体中分离得到的降三萜及其对 FAAH 的抑制活性。
Nat Prod Res. 2023 Feb;37(4):579-585. doi: 10.1080/14786419.2022.2078817. Epub 2022 May 24.
2
Triterpenoids from the fruiting bodies of Ganoderma lucidum and their inhibitory activity against FAAH.灵芝子实体中的三萜类化合物及其对 FAAH 的抑制活性。
Fitoterapia. 2022 Apr;158:105161. doi: 10.1016/j.fitote.2022.105161. Epub 2022 Feb 22.
3
Lanostane triterpenoids from Ganoderma lucidum and their inhibitory effects against FAAH.来自灵芝的羊毛甾烷三萜类化合物及其对脂肪酸酰胺水解酶的抑制作用。
Phytochemistry. 2022 Nov;203:113339. doi: 10.1016/j.phytochem.2022.113339. Epub 2022 Aug 9.
4
Leucocontextins A-R, lanostane-type triterpenoids from Ganoderma leucocontextum.白肉层孔菌素A - R,来自白肉层孔菌的羊毛甾烷型三萜类化合物。
Fitoterapia. 2016 Mar;109:91-8. doi: 10.1016/j.fitote.2015.12.004. Epub 2015 Dec 12.
5
Two new triterpenoids from fruiting bodies of fungus Ganoderma lucidum.从灵芝子实体中分离得到的两种新三萜类化合物。
J Asian Nat Prod Res. 2015;17(7):750-5. doi: 10.1080/10286020.2014.996139. Epub 2015 Jan 29.
6
New lanostane-type triterpenoids from the fruiting body of Ganoderma hainanense.来自海南灵芝子实体的新型羊毛甾烷型三萜类化合物。
Fitoterapia. 2016 Dec;115:24-30. doi: 10.1016/j.fitote.2016.09.010. Epub 2016 Sep 28.
7
Lanostane triterpenoids from the fruiting bodies of Ganoderma amboinense.来自安柄灵芝子实体的羊毛甾烷三萜。
Phytochemistry. 2024 Feb;218:113952. doi: 10.1016/j.phytochem.2023.113952. Epub 2023 Dec 12.
8
[Extraction of triterpenoids from fruiting [corrected] bodies of Ganoderma lucidum by supercritical fluid extraction].[通过超临界流体萃取从灵芝子实体中提取三萜类化合物]
Zhongguo Zhong Yao Za Zhi. 2008 Sep;33(17):2104-7.
9
Ganoderic acid Df, a new triterpenoid with aldose reductase inhibitory activity from the fruiting body of Ganoderma lucidum.灵芝中具有醛糖还原酶抑制活性的新三萜酸 Df。
Fitoterapia. 2010 Dec;81(8):1033-6. doi: 10.1016/j.fitote.2010.06.025. Epub 2010 Aug 1.
10
Cytotoxic lanostane-type triterpenoids from the fruiting bodies of Ganoderma lucidum and their structure-activity relationships.来自灵芝子实体的细胞毒性羊毛甾烷型三萜类化合物及其构效关系。
Oncotarget. 2017 Feb 7;8(6):10071-10084. doi: 10.18632/oncotarget.14336.

引用本文的文献

1
Triterpenoids from inhibit cytochrome P450 enzymes interfering with the metabolic process of specific clinical drugs.来自……的三萜类化合物抑制细胞色素P450酶,干扰特定临床药物的代谢过程。 (原文中“from”后缺少具体内容)
Front Pharmacol. 2024 Nov 15;15:1485209. doi: 10.3389/fphar.2024.1485209. eCollection 2024.
2
Endocannabinoid Hydrolase Inhibitors: Potential Novel Anxiolytic Drugs.内源性大麻素水解酶抑制剂:潜在的新型抗焦虑药物。
Drug Des Devel Ther. 2024 Jun 11;18:2143-2167. doi: 10.2147/DDDT.S462785. eCollection 2024.
3
Effect of Methyl Jasmonate Elicitation on Triterpene Production and Evaluation of Cytotoxic Activity of Mycelial Culture Extracts of (Pers.) Pat.
茉莉酸甲酯诱导对(Pers.)Pat.菌丝体培养提取物三萜产量及细胞毒性活性的影响
Plants (Basel). 2023 Jan 8;12(2):294. doi: 10.3390/plants12020294.
4
A Review of Triterpenoids and Their Bioactivities.三萜类化合物及其生物活性研究进展
Biomolecules. 2022 Dec 22;13(1):24. doi: 10.3390/biom13010024.