• 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

甲酰甲硫氨酰三肽趋化因子中Nα-阻断基团的替换:对兔中性粒细胞受体结合模式的深入了解。

Replacement of the N alpha-blocking group in the formyl-methionyl tripeptide chemoattractant: an insight into the mode of binding at the receptor on rabbit neutrophils.

作者信息

Toniolo C, Crisma M, Becker E L

机构信息

Dipartimento di Chimica Organica Università di Padova, Italy.

出版信息

Farmaco. 1990 Jul;45(7-8):921-5.

PMID:2177991
Abstract

The tripeptide N alpha-carbamoyl-L-methionyl-L-leucyl-L-phenylalanine methyl ester has been synthesized in solution by classical methods and fully characterized. This compound, prepared in order to obtain a deeper insight into the mode of binding at the formyl peptide chemotactic receptor, has been tested for its ability to induce granule enzyme secretion from rabbit peritoneal neutrophils and found to be a complete agonist. These results confirm the hypothesis that a proton on the N alpha-blocking group of the tripeptide forms a hydrogen bond with an acceptor in the binding site.

摘要

三肽Nα-氨甲酰基-L-甲硫氨酰-L-亮氨酰-L-苯丙氨酸甲酯已通过经典方法在溶液中合成并得到充分表征。制备该化合物是为了更深入地了解其在甲酰肽趋化受体上的结合模式,已测试其诱导兔腹膜中性粒细胞颗粒酶分泌的能力,结果发现它是一种完全激动剂。这些结果证实了这样的假设,即三肽Nα-封闭基团上的质子与结合位点中的受体形成氢键。

相似文献

1
Replacement of the N alpha-blocking group in the formyl-methionyl tripeptide chemoattractant: an insight into the mode of binding at the receptor on rabbit neutrophils.甲酰甲硫氨酰三肽趋化因子中Nα-阻断基团的替换:对兔中性粒细胞受体结合模式的深入了解。
Farmaco. 1990 Jul;45(7-8):921-5.
2
A conformation-activity study of the [L-(alpha Me)Phe]3 analog of the formyl methionyl tripeptide chemoattractant.
Pept Res. 1991 Mar-Apr;4(2):66-71.
3
Conformationally restricted formyl methionyl tripeptide chemoattractants: a three-dimensional structure-activity study of analogs incorporating a C alpha,alpha-dialkylated glycine at position 2.
Pept Res. 1989 Jul-Aug;2(4):275-81.
4
Synthesis, conformation, and activity of HCO-Met-delta Z Leu-Phe-OMe, an active analogue of chemotactic N-formyltripeptides.趋化性N-甲酰基三肽的活性类似物HCO-Met-δZ Leu-Phe-OMe的合成、构象及活性
Biopolymers. 1993 Mar;33(3):437-51. doi: 10.1002/bip.360330310.
5
Retro-all-D and retro isomers of a formyl-methionyl peptide chemoattractant: an insight into the mode of binding at the receptor on rabbit neutrophils.一种甲酰甲硫氨酰肽趋化因子的全反式-D型和反式异构体:对兔中性粒细胞受体结合模式的深入了解。
Biochim Biophys Acta. 1986 Dec 10;884(3):545-9. doi: 10.1016/0304-4165(86)90206-0.
6
Subtle differences between human and rabbit neutrophil receptors shown by the secretagogue activity of constrained formyl peptides.受限甲酰肽的促分泌活性显示出人类和兔中性粒细胞受体之间的细微差异。
Arch Biochem Biophys. 1997 Jan 15;337(2):267-74. doi: 10.1006/abbi.1996.9791.
7
Solid-phase synthesis of chemotactic peptides using alpha-azido acids.
J Pept Sci. 2000 Jul;6(7):314-20. doi: 10.1002/1099-1387(200007)6:7<314::AID-PSC255>3.0.CO;2-E.
8
N-terminus urea-substituted chemotactic peptides: new potent agonists and antagonists toward the neutrophil fMLF receptor.N端尿素取代的趋化肽:针对中性粒细胞fMLF受体的新型强效激动剂和拮抗剂。
J Med Chem. 1996 Mar 1;39(5):1013-5. doi: 10.1021/jm950908d.
9
Synthesis, biological activity and conformational studies of geometrically restricted tripeptide analogues of the chemoattractant HCO-Met-Leu-Phe-OMe.趋化因子HCO-甲硫氨酸-亮氨酸-苯丙氨酸-甲酯的几何受限三肽类似物的合成、生物活性及构象研究
Farmaco. 1997 Jun-Jul;52(6-7):439-44.
10
Hybrid alpha/beta3-peptides with proteinogenic side chains. Monosubstituted analogues of the chemotactic tripeptide For-Met-Leu-Phe-OMe.具有蛋白原性侧链的α/β3混合肽。趋化三肽For-Met-Leu-Phe-OMe的单取代类似物。
J Pept Sci. 2004 Aug;10(8):510-23. doi: 10.1002/psc.562.