• 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

3-取代-5-甲硫基异恶唑的合成及其驱虫活性

Synthesis and anthelmintic activity of 3-substituted 5-methylthio-isoxazoles.

作者信息

Banerjee A K, Bandyopadhyay S, Gayen A K, Sengupta T, Das A K, Chatterjee G K, Chaudhuri S K

机构信息

Organon Research Centre, Calcutta, India.

出版信息

Arzneimittelforschung. 1994 Jul;44(7):863-6.

PMID:7945524
Abstract

Isoxazole derivatives have been shown to possess antiparasitic activity. In the present study, 3-substituted 5-methylthio-isoxazoles were synthesized and tested for anthelmintic activity, along with some other isoxazoles which have been reported but not tested earlier. Nine compounds (2a, 2b, 2e, 2g, 2u, 3a, 3b, 3e and 3f) showed activity against both A. ceylanicum and N. dubius in vitro. Twelve compounds (2a, 2b, 2d, 2e, 2f, 2h, 2l, 2n, 2o, 2u, 3d and 3e) showed activity against N. dubius in vivo, a parasite of veterinary importance.

摘要

异恶唑衍生物已被证明具有抗寄生虫活性。在本研究中,合成了3-取代的5-甲硫基异恶唑并测试其驱虫活性,同时还测试了一些其他已报道但之前未测试过的异恶唑。九种化合物(2a、2b、2e、2g、2u、3a、3b、3e和3f)在体外对锡兰钩虫和杜氏小杆线虫均有活性。十二种化合物(2a、2b、2d、2e、2f、2h、2l、2n、2o、2u、3d和3e)在体内对杜氏小杆线虫有活性,杜氏小杆线虫是一种具有兽医重要性的寄生虫。

相似文献

1
Synthesis and anthelmintic activity of 3-substituted 5-methylthio-isoxazoles.3-取代-5-甲硫基异恶唑的合成及其驱虫活性
Arzneimittelforschung. 1994 Jul;44(7):863-6.
2
Synthesis and in vitro anthelmintic activity against Nippostrongylus brasiliensis of new 2-amino-4-hydroxy-delta-valerolactam derivatives.新型2-氨基-4-羟基-δ-戊内酰胺衍生物的合成及其对巴西日圆线虫的体外驱虫活性
Farmaco. 1997 Oct;52(10):603-8.
3
Synthesis of 2-carbalkoxyamino-5(6)-(1-substituted piperazin-4-yl/piperazin-4-ylcarbonyl)benzimidazoles and related compounds as potential anthelmintics.2-烷氧羰基氨基-5(6)-(1-取代哌嗪-4-基/哌嗪-4-羰基)苯并咪唑及相关化合物作为潜在驱虫剂的合成
Pharmazie. 1984 Nov;39(11):747-9.
4
Synthesis of 2,5-disubstituted benzimidazoles, 1,3,4-thiadiazoles and 3,5-diiodosalicylanilides as structural congeners of rafoxanide and closantel.
Pharmazie. 1990 Jan;45(1):34-7.
5
Anthelmintic activity of some 3-substituted phenyl-1-alkyl or phenyl propenones and propenamides.
Arzneimittelforschung. 1991 Oct;41(10):1068-71.
6
Anthelmintic activity of 6,7-diaryl-pteridines.6,7-二芳基蝶啶的驱虫活性。
Arzneimittelforschung. 1996 Jun;46(6):643-8.
7
Anthelmintic macrolactams from Nonomuraea turkmeniaca MA7381.来自土库曼诺卡氏菌MA7381的抗蠕虫大环内酯类化合物。
J Antibiot (Tokyo). 2008 Feb;61(2):59-62. doi: 10.1038/ja.2008.110.
8
Efficacy of seven anthelmintics against Ancylostoma ceylanicum in the golden hamster, Mesocricetus auratus.
Ann Trop Med Parasitol. 1978 Feb;72(1):56-8.
9
Antiparasitic agents. 5. Synthesis and anthelmintic activities of novel 2-heteroaromatic-substituted isothiocyanatobenzoxazoles and benzothiazoles.
J Med Chem. 1982 Aug;25(8):969-74. doi: 10.1021/jm00350a017.
10
Synthesis and anthelmintic activity of 3,6-disubstituted-7H-s-triazolo(3,4-b)(1,3,4)thiadiazines.3,6-二取代-7H-1,2,4-三唑并[3,4-b][1,3,4]噻二嗪的合成及其驱虫活性
Arzneimittelforschung. 2001;51(7):569-73. doi: 10.1055/s-0031-1300081.

引用本文的文献

1
5-Amino-3-methyl-1,2-oxazole-4-carbonitrile.5-氨基-3-甲基-1,2-恶唑-4-腈
Acta Crystallogr Sect E Struct Rep Online. 2012 Aug 1;68(Pt 8):o2530. doi: 10.1107/S1600536812032667. Epub 2012 Jul 25.