• 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

新型 4-吡唑啉-3-基-1,2,3-三唑和 1,2,3-三唑-4-基-吡唑啉-1-基噻唑的设计与合成作为潜在的抗菌剂。

Design and synthesis of new 4-pyrazolin-3-yl-1,2,3-triazoles and 1,2,3-triazol-4-yl-pyrazolin-1-ylthiazoles as potential antimicrobial agents.

机构信息

Applied Organic Chemistry Department, National Research Centre, Dokki, 12622 Giza, Egypt.

出版信息

Eur J Med Chem. 2012 Jun;52:263-8. doi: 10.1016/j.ejmech.2012.03.023. Epub 2012 Mar 23.

DOI:10.1016/j.ejmech.2012.03.023
PMID:22480494
Abstract

New pyrazolyl-1,2,3-triazoles and 1,2,3-triazol-4-yl-pyrazolylthiazoles were synthesized through multi step reactions using 1-tolylyl-4-acetyl-5-methyl-1,2,3-triazole as a precursor. All the newly synthesized compounds were characterized by spectral and elemental analyses. The structure of 11b was evidenced by X-ray crystallographic study. The newly synthesized compounds were evaluated for their antimicrobial activities and also their minimum inhibitory concentration (MIC) against most of test organisms was performed. Amongst the tested compounds 5a, 5c, 11b and 11c displayed excellent antimicrobial activity.

摘要

新型吡唑基-1,2,3-三唑和 1,2,3-三唑-4-基-吡唑基噻唑是通过多步反应合成的,使用 1-甲苯基-4-乙酰基-5-甲基-1,2,3-三唑作为前体。所有新合成的化合物都通过光谱和元素分析进行了表征。11b 的结构通过 X 射线晶体学研究得到了证实。新合成的化合物进行了抗菌活性评价,对大多数测试生物进行了最低抑菌浓度(MIC)测定。在所测试的化合物中,5a、5c、11b 和 11c 表现出优异的抗菌活性。

相似文献

1
Design and synthesis of new 4-pyrazolin-3-yl-1,2,3-triazoles and 1,2,3-triazol-4-yl-pyrazolin-1-ylthiazoles as potential antimicrobial agents.新型 4-吡唑啉-3-基-1,2,3-三唑和 1,2,3-三唑-4-基-吡唑啉-1-基噻唑的设计与合成作为潜在的抗菌剂。
Eur J Med Chem. 2012 Jun;52:263-8. doi: 10.1016/j.ejmech.2012.03.023. Epub 2012 Mar 23.
2
Synthesis of some new 1,3,4-thiadiazol-2-ylmethyl-1,2,4-triazole derivatives and investigation of their antimicrobial activities.一些新型1,3,4-噻二唑-2-基甲基-1,2,4-三唑衍生物的合成及其抗菌活性研究
Eur J Med Chem. 2009 Jul;44(7):2896-903. doi: 10.1016/j.ejmech.2008.12.005. Epub 2008 Dec 16.
3
Design, synthesis and antimicrobial activities of some new quinoline derivatives carrying 1,2,3-triazole moiety.设计、合成及含 1,2,3-三唑基的一些新喹啉衍生物的抗菌活性。
Eur J Med Chem. 2010 Sep;45(9):3803-10. doi: 10.1016/j.ejmech.2010.05.030. Epub 2010 May 20.
4
Design, synthesis of some new (2-aminothiazol-4-yl)methylester derivatives as possible antimicrobial and antitubercular agents.设计、合成一些新的(2-氨基噻唑-4-基)甲酯衍生物作为可能的抗菌和抗结核药物。
Eur J Med Chem. 2012 Mar;49:172-82. doi: 10.1016/j.ejmech.2012.01.008. Epub 2012 Jan 12.
5
Synthesis of some new 1,2,4-triazoles, their Mannich and Schiff bases and evaluation of their antimicrobial activities.一些新型1,2,4-三唑及其曼尼希碱和席夫碱的合成及其抗菌活性评估。
Eur J Med Chem. 2009 Mar;44(3):1057-66. doi: 10.1016/j.ejmech.2008.06.019. Epub 2008 Jun 26.
6
Hybrids of ravuconazole: synthesis and biological evaluation.雷夫康唑的杂种:合成与生物评价。
Eur J Med Chem. 2012 Aug;54:295-302. doi: 10.1016/j.ejmech.2012.05.010. Epub 2012 May 15.
7
Synthesis and antimicrobial activity evaluation of new 1,2,4-triazoles and 1,3,4-thiadiazoles bearing imidazo[2,1-b]thiazole moiety.含咪唑并[2,1-b]噻唑部分的新型 1,2,4-三唑和 1,3,4-噻二唑的合成及抗菌活性评价。
Eur J Med Chem. 2010 Jan;45(1):63-8. doi: 10.1016/j.ejmech.2009.09.024. Epub 2009 Sep 16.
8
Regioselective reaction: synthesis, characterization and pharmacological studies of some new Mannich bases derived from 1,2,4-triazoles.区域选择性反应:一些源自1,2,4-三唑的新型曼尼希碱的合成、表征及药理学研究
Eur J Med Chem. 2009 Sep;44(9):3784-7. doi: 10.1016/j.ejmech.2009.04.038. Epub 2009 May 5.
9
Synthesis and biological evaluation of indole containing derivatives of thiosemicarbazide and their cyclic 1,2,4-triazole and 1,3,4-thiadiazole analogs.含吲哚的氨基硫脲衍生物及其环状1,2,4-三唑和1,3,4-噻二唑类似物的合成与生物学评价
Arzneimittelforschung. 2000 Jan;50(1):48-54. doi: 10.1055/s-0031-1300163.
10
Synthesis and antimicrobial activity of 4-phenyl/cyclohexyl-5-(1-phenoxyethyl)-3-[N-(2-thiazolyl)acetamido]thio-4H-1,2,4-triazole derivatives.4-苯基/环己基-5-(1-苯氧基乙基)-3-[N-(2-噻唑基)乙酰胺基]硫代-4H-1,2,4-三唑衍生物的合成与抗菌活性
Eur J Med Chem. 2005 Jun;40(6):607-13. doi: 10.1016/j.ejmech.2005.01.007. Epub 2005 Mar 2.

引用本文的文献

1
Facile Epitaxial Growth of Novel Nanoscale Ag-MAFs on Reverse Osmosis Membranes: Enhancing Performance, Antibacterial Activity, and (Bio)fouling Resistance.新型纳米级银-金属有机框架在反渗透膜上的简便外延生长:提高性能、抗菌活性及抗(生物)污染能力
ACS Omega. 2025 Jun 23;10(26):28191-28209. doi: 10.1021/acsomega.5c02816. eCollection 2025 Jul 8.
2
Utilizing perhalopyridine-based alkynes as suitable precursors for the synthesis of novel poly(1,2,3-triazolyl)-substituted perhalopyridines.利用基于全卤代吡啶的炔烃作为合成新型聚(1,2,3 - 三唑基)取代全卤代吡啶的合适前体。
RSC Adv. 2024 Sep 27;14(42):30873-30885. doi: 10.1039/d4ra05861e. eCollection 2024 Sep 24.
3
Development in the Synthesis of Bioactive Thiazole-Based Heterocyclic Hybrids Utilizing Phenacyl Bromide.
利用溴代苯乙酮合成具有生物活性的噻唑基杂环衍生物的研究进展。
ACS Omega. 2024 Apr 16;9(17):18709-18746. doi: 10.1021/acsomega.3c10299. eCollection 2024 Apr 30.
4
Diverse Pharmacological Potential of different Substituted Pyrazole Derivatives.不同取代吡唑衍生物的多样化药理学潜力。
Curr Org Synth. 2024;21(7):858-888. doi: 10.2174/0115701794260444230925095804.
5
Biochemical and inhibition of bovine and human carbonic anhydrase-II by 1H-1,2,3-triazole analogs.1H-1,2,3-三唑类似物对牛和人碳酸酐酶-II的生化作用及抑制作用
Front Chem. 2022 Nov 25;10:1072337. doi: 10.3389/fchem.2022.1072337. eCollection 2022.
6
Identifying a Hidden Conglomerate Chiral Pool in the CSD.在剑桥晶体结构数据库中识别一个隐藏的聚集手性库。
JACS Au. 2022 Sep 23;2(10):2235-2250. doi: 10.1021/jacsau.2c00394. eCollection 2022 Oct 24.
7
Synthesis and antimicrobial activity of 1-1,2,3-triazole and carboxylate analogues of metronidazole.甲硝唑的1,2,3-三唑和羧酸盐类似物的合成及其抗菌活性
Beilstein J Org Chem. 2021 Sep 9;17:2377-2384. doi: 10.3762/bjoc.17.154. eCollection 2021.
8
Synthesis of New 1-1,2,3-Triazole Analogs in Aqueous Medium "" Chemistry: A Novel Class of Potential Carbonic Anhydrase-II Inhibitors.水相中新型1,2,3-三唑类似物的合成:化学——一类新型潜在的碳酸酐酶-II抑制剂
Front Chem. 2021 Jun 30;9:642614. doi: 10.3389/fchem.2021.642614. eCollection 2021.
9
Novel quinolinone-pyrazoline hybrids: synthesis and evaluation of antioxidant and lipoxygenase inhibitory activity.新型喹啉酮-吡唑啉杂合体的合成及其抗氧化和脂氧合酶抑制活性的评价。
Mol Divers. 2021 May;25(2):723-740. doi: 10.1007/s11030-020-10045-x. Epub 2020 Feb 17.
10
Synthetic approaches, structure activity relationship and biological applications for pharmacologically attractive pyrazole/pyrazoline-thiazolidine-based hybrids.基于具有药理活性的吡唑/吡唑啉-噻唑烷杂化物的合成方法、构效关系及生物学应用
Eur J Med Chem. 2016 May 4;113:145-66. doi: 10.1016/j.ejmech.2016.02.030. Epub 2016 Feb 16.