• 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

Design and synthesis of conformationally-constrained MMP inhibitors.

作者信息

Natchus M G, Cheng M, Wahl C T, Pikul S, Almstead N G, Bradley R S, Taiwo Y O, Mieling G E, Dunaway C M, Snider C E, McIver J M, Barnett B L, McPhail S J, Anastasio M B, De B

机构信息

Procter and Gamble Pharmaceuticals, Health Care Research Center, Mason, OH 45040, USA.

出版信息

Bioorg Med Chem Lett. 1998 Aug 18;8(16):2077-80. doi: 10.1016/s0960-894x(98)00370-9.

DOI:10.1016/s0960-894x(98)00370-9
PMID:9873489
Abstract

A novel series of conformationally constrained matrix metalloprotease inhibitors was identified. The potencies observed for these inhibitors were highly dependent upon the substitution pattern on the caprolactam ring as well as the succinate moiety.

摘要

相似文献

1
Design and synthesis of conformationally-constrained MMP inhibitors.
Bioorg Med Chem Lett. 1998 Aug 18;8(16):2077-80. doi: 10.1016/s0960-894x(98)00370-9.
2
Structure-based design and synthesis of a series of hydroxamic acids with a quaternary-hydroxy group in P1 as inhibitors of matrix metalloproteinases.基于结构设计并合成一系列在P1位带有季羟基的异羟肟酸作为基质金属蛋白酶抑制剂。
Bioorg Med Chem Lett. 1998 Apr 7;8(7):837-42. doi: 10.1016/s0960-894x(98)00125-5.
3
The asymmetric synthesis and in vitro characterization of succinyl mercaptoalcohol and mercaptoketone inhibitors of matrix metalloproteinases.
Bioorg Med Chem Lett. 1998 May 19;8(10):1163-8. doi: 10.1016/s0960-894x(98)00186-3.
4
The design, synthesis, and structure-activity relationships of a series of macrocyclic MMP inhibitors.
Bioorg Med Chem Lett. 1998 Aug 18;8(16):2087-92. doi: 10.1016/s0960-894x(98)00396-5.
5
Design and synthesis of matrix metalloproteinase inhibitors guided by molecular modeling. Picking the S(1) pocket using conformationally constrained inhibitors.
J Med Chem. 2001 Sep 13;44(19):3074-82. doi: 10.1021/jm010096n.
6
The next generation of MMP inhibitors. Design and synthesis.
Ann N Y Acad Sci. 1999 Jun 30;878:40-60. doi: 10.1111/j.1749-6632.1999.tb07673.x.
7
N-Aryl sulfonyl homocysteine hydroxamate inhibitors of matrix metalloproteinases: further probing of the S(1), S(1)', and S(2)' pockets.基质金属蛋白酶的N-芳基磺酰基高半胱氨酸异羟肟酸酯抑制剂:对S(1)、S(1)'和S(2)'口袋的进一步探索
J Med Chem. 2001 Sep 13;44(19):3066-73. doi: 10.1021/jm010097f.
8
Phosphinic acid-based MMP-13 inhibitors that spare MMP-1 and MMP-3.
Bioorg Med Chem Lett. 2003 Jul 21;13(14):2331-6. doi: 10.1016/s0960-894x(03)00413-x.
9
Discovery of potent, achiral matrix metalloproteinase inhibitors.强效非手性基质金属蛋白酶抑制剂的发现。
J Med Chem. 1998 Sep 10;41(19):3568-71. doi: 10.1021/jm980253r.
10
Malonyl alpha-mercaptoketones and alpha-mercaptoalcohols, a new class of matrix metalloproteinase inhibitors.丙二酰α-巯基酮和α-巯基醇,一类新型基质金属蛋白酶抑制剂。
Bioorg Med Chem Lett. 1998 May 19;8(10):1157-62. doi: 10.1016/s0960-894x(98)00185-1.

引用本文的文献

1
Methanethiol Binding Strengths and Deprotonation Energies in Zn(II)-Imidazole Complexes from M05-2X and MP2 Theories: Coordination Number and Geometry Influences Relevant to Zinc Enzymes.基于M05 - 2X和MP2理论的Zn(II)-咪唑配合物中甲硫醇的结合强度与去质子化能:与锌酶相关的配位数和几何结构影响
J Phys Chem B. 2015 Sep 17;119(37):12182-92. doi: 10.1021/acs.jpcb.5b07115. Epub 2015 Sep 4.
2
Molecular docking studies of a group of hydroxamate inhibitors with gelatinase-A by molecular dynamics.通过分子动力学对一组异羟肟酸酯抑制剂与明胶酶-A进行分子对接研究。
J Comput Aided Mol Des. 2002 Jan;16(1):27-41. doi: 10.1023/a:1016345810973.