• 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

[查耳酮及其杂环类似物作为潜在的抗真菌化疗药物]

[Chalcones and their heterocyclic analogs as potential antifungal chemotherapeutic agents].

作者信息

Opletalová V, Sedivý D

机构信息

Katedra farmaceutické chemie a kontroly léciv, Farmaceutické fakulty, Univerzity Karlovy, Hradec Králové.

出版信息

Ceska Slov Farm. 1999 Nov;48(6):252-5.

PMID:10748740
Abstract

Chalcones and their heterocyclic analogues show various biological effects, e.g. anti-inflammatory, antitumour, antibacterial, antituberculous, antiviral, antiprotozoal, gastroprotective, and others. The present review discusses in greater detail the fungistatic and fungicide properties of these compounds and presents also their chemical structures. The mechanism of antifungal effects of chalcones and their analogues has not been investigated in greater detail. Due to the presence of a reactive ketovinyl moiety in the molecule the compounds of this type are able to react with the thiol groups of enzymes. It cannot be excluded that chalcones interfere with the normal function of the membranes of fungi and moulds. Further investigation of chemical, physical, and biological properties of chalcones and their analogues could lead to the elucidation of the mechanism of their action and finding of effective fungicidal and fungistatic agents in this group of organic substances.

摘要

查耳酮及其杂环类似物具有多种生物学效应,如抗炎、抗肿瘤、抗菌、抗结核、抗病毒、抗原虫、胃保护等。本综述更详细地讨论了这些化合物的抑菌和杀菌特性,并介绍了它们的化学结构。查耳酮及其类似物的抗真菌作用机制尚未得到更深入的研究。由于该类分子中存在反应性酮乙烯基部分,这类化合物能够与酶的巯基发生反应。不能排除查耳酮会干扰真菌和霉菌膜的正常功能。进一步研究查耳酮及其类似物的化学、物理和生物学性质,可能会阐明其作用机制,并在这组有机物质中找到有效的杀菌和抑菌剂。

相似文献

1
[Chalcones and their heterocyclic analogs as potential antifungal chemotherapeutic agents].[查耳酮及其杂环类似物作为潜在的抗真菌化疗药物]
Ceska Slov Farm. 1999 Nov;48(6):252-5.
2
[Chalcones and their heterocyclic analogs as potential therapeutic agents in bacterial diseases].[查尔酮及其杂环类似物作为细菌性疾病的潜在治疗药物]
Ceska Slov Farm. 2000 Nov;49(6):278-84.
3
Antifungal activity and studies on mode of action of novel xanthoxyline-derived chalcones.新型花椒碱衍生查尔酮的抗真菌活性及作用方式研究
Arch Pharm (Weinheim). 2005 Mar;338(2-3):87-95. doi: 10.1002/ardp.200400929.
4
[Chalcones (1,3-diarylpropen-1-ones) and their analogs as potential therapeutic agents in cardiovascular system diseases].[查耳酮(1,3 - 二芳基丙烯 - 1 - 酮)及其类似物作为心血管系统疾病的潜在治疗药物]
Ceska Slov Farm. 2003 Jan;52(1):12-9.
5
Antifungal activity of chalcones: a mechanistic study using various yeast strains.查耳酮的抗真菌活性:使用多种酵母菌株的机制研究
Eur J Med Chem. 2008 Oct;43(10):2220-8. doi: 10.1016/j.ejmech.2007.12.027. Epub 2008 Jan 12.
6
[Recent advances in the study of antifungal lead compounds with new chemical scaffolds].[新型化学骨架抗真菌先导化合物的研究进展]
Yao Xue Xue Bao. 2007 Nov;42(11):1129-36.
7
Synthesis and antimicrobial studies on novel chloro-fluorine containing hydroxy pyrazolines.新型含氯氟羟基吡唑啉的合成与抗菌研究
Eur J Med Chem. 2007 Jan;42(1):30-6. doi: 10.1016/j.ejmech.2006.07.011. Epub 2006 Sep 26.
8
Synthesis, physicochemical properties and antimicrobial evaluation of new (E)-chalcones.新型(E)-查尔酮的合成、理化性质及抗菌性能评价
Eur J Med Chem. 2008 Apr;43(4):707-13. doi: 10.1016/j.ejmech.2007.05.006. Epub 2007 Jun 2.
9
Novel 2'-hydroxylfurylchalcones: synthesis and biological activity.新型 2'-羟基呋喃查尔酮:合成与生物活性。
Carbohydr Res. 2010 Sep 3;345(13):1872-6. doi: 10.1016/j.carres.2010.05.017. Epub 2010 May 23.
10
Antifungal activity of Zuccagnia punctata Cav.: evidence for the mechanism of action.蓬尾苏卡尼亚的抗真菌活性:作用机制的证据
Planta Med. 2007 Aug;73(10):1074-80. doi: 10.1055/s-2007-981561. Epub 2007 Jul 12.

引用本文的文献

1
Crystal structure and Hirshfeld-surface analysis of 1-(4-fluoro-phen-yl)-3,3-bis-(methyl-sulfan-yl)prop-2-en-1-one.1-(4-氟苯基)-3,3-双(甲基硫烷基)丙-2-烯-1-酮的晶体结构与 Hirshfeld 表面分析
Acta Crystallogr E Crystallogr Commun. 2025 May 13;81(Pt 6):516-519. doi: 10.1107/S2056989025004189. eCollection 2025 Jun 1.
2
Suppressive Effects of TSAHC in an Experimental Mouse Model and Fibroblast-Like Synoviocytes of Rheumatoid Arthritis.TSAHC 在实验性关节炎小鼠模型和类风湿关节炎成纤维样滑膜细胞中的抑制作用。
Inflammation. 2017 Dec;40(6):1825-1835. doi: 10.1007/s10753-017-0621-6.
3
Crystal structures of (2E)-1-(3-bromo-thio-phen-2-yl)-3-(2-meth-oxy-phen-yl)prop-2-en-1-one and (2E)-1-(3-bromo-thio-phen-2-yl)-3-(3,4-di-meth-oxy-phen-yl)prop-2-en-1-one.
(2E)-1-(3-溴噻吩-2-基)-3-(2-甲氧基苯基)丙-2-烯-1-酮和(2E)-1-(3-溴噻吩-2-基)-3-(3,4-二甲氧基苯基)丙-2-烯-1-酮的晶体结构
Acta Crystallogr E Crystallogr Commun. 2015 Jul 25;71(Pt 8):965-71. doi: 10.1107/S2056989015013420. eCollection 2015 Aug 1.
4
(E)-1-([1,1'-Biphen-yl]-4-yl)-3-(2-methyl-phen-yl)prop-2-en-1-one.(E)-1-([1,1'-联苯]-4-基)-3-(2-甲基苯基)丙-2-烯-1-酮
Acta Crystallogr Sect E Struct Rep Online. 2014 Jun 25;70(Pt 7):o809-10. doi: 10.1107/S1600536814014317. eCollection 2014 Jul 1.
5
High-throughput screen of natural product libraries for hsp90 inhibitors.高通量筛选天然产物文库以寻找 HSP90 抑制剂。
Biology (Basel). 2014 Feb 10;3(1):101-38. doi: 10.3390/biology3010101.
6
(E)-3-(4-Chloro-phen-yl)-1-(5-hy-droxy-2,2-dimethyl-2H-chromen-6-yl)prop-2-en-1-one.(E)-3-(4-氯苯基)-1-(5-羟基-2,2-二甲基-2H-色烯-6-基)丙-2-烯-1-酮
Acta Crystallogr Sect E Struct Rep Online. 2012 Feb 1;68(Pt 2):o278. doi: 10.1107/S1600536811055255. Epub 2012 Jan 7.
7
2,3-Dibromo-1,3-bis-(4-chloro-phen-yl)propan-1-one.2,3-二溴-1,3-双(4-氯苯基)丙-1-酮
Acta Crystallogr Sect E Struct Rep Online. 2010 Nov 13;66(Pt 12):o3131. doi: 10.1107/S1600536810045022.
8
A second polymorph of (2E)-1-(4-fluoro-phen-yl)-3-(3,4,5-trimethoxy-phen-yl)prop-2-en-1-one.(2E)-1-(4-氟苯基)-3-(3,4,5-三甲氧基苯基)丙-2-烯-1-酮的第二种多晶型物。
Acta Crystallogr Sect E Struct Rep Online. 2009 Jul 25;65(Pt 8):o1965-6. doi: 10.1107/S1600536809028517.
9
(2E)-3-(2-Chloro-6-methyl-3-quinol-yl)-1-(1-naphth-yl)prop-2-en-1-one.(2E)-3-(2-氯-6-甲基-3-喹啉基)-1-(1-萘基)丙-2-烯-1-酮
Acta Crystallogr Sect E Struct Rep Online. 2010 Mar 6;66(Pt 4):o761. doi: 10.1107/S1600536810007828.
10
(E)-3-[4-(Dimethyl-amino)phen-yl]-1-(4-methyl-phen-yl)prop-2-en-1-one.(E)-3-[4-(二甲基氨基)苯基]-1-(4-甲基苯基)丙-2-烯-1-酮
Acta Crystallogr Sect E Struct Rep Online. 2009 Dec 16;66(Pt 1):o174. doi: 10.1107/S1600536809052398.