• 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

Synthesis and evaluation of chloromethyl sulfoxides as a new class of selective irreversible cysteine protease inhibitors.

作者信息

Brouwer Arwin J, Bunschoten Anton, Liskamp Rob M J

机构信息

Department of Medicinal Chemistry and Chemical Biology, Utrecht Institute for Pharmaceutical Sciences, Utrecht University, PO Box 80082, NL-3508 TB Utrecht, The Netherlands.

出版信息

Bioorg Med Chem. 2007 Nov 15;15(22):6985-93. doi: 10.1016/j.bmc.2007.07.045. Epub 2007 Aug 22.

DOI:10.1016/j.bmc.2007.07.045
PMID:17869119
Abstract

The synthesis and biological evaluation of a new class of selective irreversible cysteine protease inhibitors is described. A set of amino acid based chloromethyl sulfoxides was prepared and they were found to inhibit irreversibly the cysteine protease papain. They were selective for cysteine proteases since no inhibition was found for the serine protease chymotrypsin.

摘要

相似文献

1
Synthesis and evaluation of chloromethyl sulfoxides as a new class of selective irreversible cysteine protease inhibitors.
Bioorg Med Chem. 2007 Nov 15;15(22):6985-93. doi: 10.1016/j.bmc.2007.07.045. Epub 2007 Aug 22.
2
New peptidic cysteine protease inhibitors derived from the electrophilic alpha-amino acid aziridine-2,3-dicarboxylic acid.源自亲电α-氨基酸氮丙啶-2,3-二羧酸的新型肽类半胱氨酸蛋白酶抑制剂。
J Med Chem. 1999 Feb 25;42(4):560-72. doi: 10.1021/jm981061z.
3
Peptidyl beta-homo-aspartals (3-amino-4-carboxybutyraldehydes): new specific inhibitors of caspases.肽基β-高天冬氨酸醛(3-氨基-4-羧基丁醛):新型半胱天冬酶特异性抑制剂。
Biopolymers. 1999;51(1):109-18. doi: 10.1002/(SICI)1097-0282(1999)51:1<109::AID-BIP12>3.0.CO;2-S.
4
Inhibition of cysteine proteases by peptides containing aziridine-2,3-dicarboxylic acid building blocks.含氮丙啶-2,3-二羧酸结构单元的肽对半胱氨酸蛋白酶的抑制作用。
Biopolymers. 1999;51(1):87-97. doi: 10.1002/(SICI)1097-0282(1999)51:1<87::AID-BIP10>3.0.CO;2-Z.
5
Design of potent, selective, and orally bioavailable inhibitors of cysteine protease cathepsin k.半胱氨酸蛋白酶组织蛋白酶K的高效、选择性及口服生物可利用抑制剂的设计
J Med Chem. 2004 Jan 29;47(3):588-99. doi: 10.1021/jm030373l.
6
Structure-based design, synthesis, and biological evaluation of irreversible human rhinovirus 3C protease inhibitors. 4. Incorporation of P1 lactam moieties as L-glutamine replacements.基于结构的不可逆人鼻病毒3C蛋白酶抑制剂的设计、合成及生物学评价。4. 引入P1内酰胺基团作为L-谷氨酰胺替代物。
J Med Chem. 1999 Apr 8;42(7):1213-24. doi: 10.1021/jm9805384.
7
Synthesis and biological evaluation of reversible inhibitors of IdeS, a bacterial cysteine protease and virulence determinant.细菌半胱氨酸蛋白酶及毒力决定因素IdeS的可逆抑制剂的合成与生物学评价
Bioorg Med Chem. 2009 May 1;17(9):3463-70. doi: 10.1016/j.bmc.2009.03.026. Epub 2009 Mar 19.
8
Design, synthesis, and evaluation of aza-peptide epoxides as selective and potent inhibitors of caspases-1, -3, -6, and -8.氮杂肽环氧化物作为半胱天冬酶-1、-3、-6和-8的选择性强效抑制剂的设计、合成与评估
J Med Chem. 2004 Mar 11;47(6):1553-74. doi: 10.1021/jm0305016.
9
Aza-peptide epoxides: a new class of inhibitors selective for clan CD cysteine proteases.氮杂肽环氧化物:一类对CD家族半胱氨酸蛋白酶具有选择性的新型抑制剂。
J Med Chem. 2002 Nov 7;45(23):4958-60. doi: 10.1021/jm025581c.
10
eta(1)-N-succinimidato complexes of iron, molybdenum and tungsten as reversible inhibitors of papain.铁、钼和钨的η(1)-N-琥珀酰亚胺基配合物作为木瓜蛋白酶的可逆抑制剂
J Inorg Biochem. 2009 Aug;103(8):1162-8. doi: 10.1016/j.jinorgbio.2009.06.004. Epub 2009 Jun 25.