• 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

一系列强效且口服生物可利用的凝血酶抑制剂的合成,这些抑制剂在P3位置利用3,3-二取代丙酸衍生物。

Synthesis of a series of potent and orally bioavailable thrombin inhibitors that utilize 3,3-disubstituted propionic acid derivatives in the P3 position.

作者信息

Tucker T J, Lumma W C, Lewis S D, Gardell S J, Lucas B J, Sisko J T, Lynch J J, Lyle E A, Baskin E P, Woltmann R F, Appleby S D, Chen I W, Dancheck K B, Naylor-Olsen A M, Krueger J A, Cooper C M, Vacca J P

机构信息

Department of Medicinal Chemistry, Merck Research Laboratories, West Point, Pennsylvania 19486, USA.

出版信息

J Med Chem. 1997 Oct 24;40(22):3687-93. doi: 10.1021/jm970397q.

DOI:10.1021/jm970397q
PMID:9357536
Abstract

As part of an effort to prepare efficacious and orally bioavailable analogs of the previously reported thrombin inhibitors 1a, b, we have synthesized a series of compounds that utilize 3,3-disubstituted propionic acid derivatives as P3 ligands. By removing the N-terminal amino group, the general oral bioavailability of this class of compounds was enhanced without excessively increasing the lipophilicity of the compounds. The overall properties of the molecules could be drastically altered depending on the nature of the groups substituted onto the 3-position of the P3 propionic acid moiety. A number of the compounds exhibited good oral bioavailability in rats and dogs, and numerous compounds were efficacious in a rat FeCl3-induced model of arterial thrombosis. Compound 7, the 3,3-diphenylpropionic acid derivative, showed the best overall profile of in vivo and in vitro activity. Molecular modeling studies suggest that these compounds bind in the thrombin active site in a manner essentially identical to that previously reported for compound 1a.

摘要

作为制备先前报道的凝血酶抑制剂1a、b的有效且口服生物可利用类似物工作的一部分,我们合成了一系列利用3,3-二取代丙酸衍生物作为P3配体的化合物。通过去除N-末端氨基,这类化合物的总体口服生物利用度得到提高,而不会过度增加化合物的亲脂性。分子的整体性质会根据取代在P3丙酸部分3-位上的基团性质而发生巨大变化。许多化合物在大鼠和狗中表现出良好的口服生物利用度,并且许多化合物在大鼠FeCl3诱导的动脉血栓形成模型中有效。化合物7,即3,3-二苯基丙酸衍生物,显示出最佳的体内和体外活性总体概况。分子模拟研究表明,这些化合物在凝血酶活性位点的结合方式与先前报道的化合物1a基本相同。

相似文献

1
Synthesis of a series of potent and orally bioavailable thrombin inhibitors that utilize 3,3-disubstituted propionic acid derivatives in the P3 position.一系列强效且口服生物可利用的凝血酶抑制剂的合成,这些抑制剂在P3位置利用3,3-二取代丙酸衍生物。
J Med Chem. 1997 Oct 24;40(22):3687-93. doi: 10.1021/jm970397q.
2
Potent noncovalent thrombin inhibitors that utilize the unique amino acid D-dicyclohexylalanine in the P3 position. Implications on oral bioavailability and antithrombotic efficacy.在P3位置利用独特氨基酸D-二环己基丙氨酸的强效非共价凝血酶抑制剂。对口服生物利用度和抗血栓形成疗效的影响。
J Med Chem. 1997 May 23;40(11):1565-9. doi: 10.1021/jm970140s.
3
Design and synthesis of a series of potent and orally bioavailable noncovalent thrombin inhibitors that utilize nonbasic groups in the P1 position.一系列利用P1位非碱性基团的高效且口服生物可利用的非共价凝血酶抑制剂的设计与合成。
J Med Chem. 1998 Aug 13;41(17):3210-9. doi: 10.1021/jm9801713.
4
Efficacious and orally bioavailable thrombin inhibitors based on a 2,5-thienylamidine at the P1 position: discovery of N-carboxymethyl-d-diphenylalanyl-l-prolyl[(5-amidino-2-thienyl)methyl]amide.基于P1位2,5-噻吩脒的有效且口服生物可利用的凝血酶抑制剂:N-羧甲基-d-二苯基丙氨酰-l-脯氨酰[(5-脒基-2-噻吩基)甲基]酰胺的发现。
J Med Chem. 2003 Aug 14;46(17):3612-22. doi: 10.1021/jm030025j.
5
Synthesis and evaluation of novel alpha-heteroaryl-phenylpropanoic acid derivatives as PPARalpha/gamma dual agonists.新型 α-杂芳基-苯基丙酸衍生物的合成与评价及其作为过氧化物酶体增殖物激活受体 α/γ 双重激动剂的活性。
Bioorg Med Chem. 2009 Oct 15;17(20):7113-25. doi: 10.1016/j.bmc.2009.09.001. Epub 2009 Sep 6.
6
Metabolism-directed optimization of 3-aminopyrazinone acetamide thrombin inhibitors. Development of an orally bioavailable series containing P1 and P3 pyridines.3-氨基吡嗪酮乙酰胺凝血酶抑制剂的代谢导向优化。含P1和P3吡啶的口服生物利用度系列药物的开发。
J Med Chem. 2003 Feb 13;46(4):461-73. doi: 10.1021/jm020311f.
7
Rational design, synthesis, and structure-activity relationships of novel factor Xa inhibitors: (2-substituted-4-amidinophenyl)pyruvic and -propionic acids.新型Xa因子抑制剂的合理设计、合成及构效关系:(2-取代-4-脒基苯基)丙酮酸和丙酸
J Med Chem. 2003 May 8;46(10):1845-57. doi: 10.1021/jm020485x.
8
P3 optimization of functional potency, in vivo efficacy and oral bioavailability in 3-aminopyrazinone thrombin inhibitors bearing non-charged groups at the P1 position.在 P1 位带有非电荷基团的 3-氨基吡嗪酮类凝血酶抑制剂中优化功能效力、体内疗效和口服生物利用度。
Bioorg Med Chem Lett. 2011 Mar 1;21(5):1532-5. doi: 10.1016/j.bmcl.2010.12.108. Epub 2010 Dec 28.
9
Design, synthesis and biological activity of amidinobicyclic compounds (derivatives of DX-9065a) as factor Xa inhibitors: SAR study of S1 and aryl binding sites.作为凝血因子Xa抑制剂的脒基双环化合物(DX-9065a衍生物)的设计、合成及生物活性:S1和芳基结合位点的构效关系研究
Bioorg Med Chem. 2004 May 1;12(9):2099-114. doi: 10.1016/j.bmc.2004.02.032.
10
Discovery of a novel, selective, and orally bioavailable class of thrombin inhibitors incorporating aminopyridyl moieties at the P1 position.发现一类新型、选择性且口服生物可利用的凝血酶抑制剂,其在P1位含有氨基吡啶基部分。
J Med Chem. 1997 Nov 7;40(23):3726-33. doi: 10.1021/jm970493r.

引用本文的文献

1
Palladium-catalyzed asymmetric allylic 4-pyridinylation via electroreductive substitution reaction.钯催化的不对称烯丙基 4-吡啶化反应通过电还原取代反应。
Nat Commun. 2022 Sep 26;13(1):5642. doi: 10.1038/s41467-022-33452-0.