• 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

某些缓激肽类似物对激肽酶II的稳定性(作者译)

[Stability of some bradykinin analogues against kininase II (author's transl)].

作者信息

Reissmann S, Paegelov I, Leisner H, Arold H

出版信息

Experientia. 1975 Dec 15;31(12):1395-6. doi: 10.1007/BF01923205.

DOI:10.1007/BF01923205
PMID:174930
Abstract

Some analogues of bradykinin, especially with replacements by other amino acids of phenylalanine in position 8, have been investigated for enzymatic stability against kininase II from rat duodenum microsomes and rat uterus plasma membranes, respectively. As compared with bradykinin, two of the analogues, [8-erythro-beta-phenylserine]- and [8-erythro-alpha-Amino-beta-phenylbutyric acid]-Bradykinin were stable to enzymatic degradation. Therefore, the latter may be used for studies in hormone-receptor interaction.

摘要

已分别研究了一些缓激肽类似物,尤其是8位苯丙氨酸被其他氨基酸取代的类似物,对来自大鼠十二指肠微粒体和大鼠子宫质膜的激肽酶II的酶稳定性。与缓激肽相比,两种类似物,[8-赤藓糖-β-苯丝氨酸]-和[8-赤藓糖-α-氨基-β-苯丁酸]-缓激肽对酶促降解具有稳定性。因此,后者可用于激素-受体相互作用的研究。

相似文献

1
[Stability of some bradykinin analogues against kininase II (author's transl)].某些缓激肽类似物对激肽酶II的稳定性(作者译)
Experientia. 1975 Dec 15;31(12):1395-6. doi: 10.1007/BF01923205.
2
[Studies on bradykinin-binding cell fractions. 1. Characterization of kininase activity of the microsomal and membrane fraction from the rat uterus].[缓激肽结合细胞组分的研究。1. 大鼠子宫微粒体和膜组分激肽酶活性的特性]
Acta Biol Med Ger. 1975;34(1):9-13.
3
[On the mode of action of bradykinin on smooth muscle (author's transl)].[关于缓激肽对平滑肌的作用方式(作者译)]
Pharmazie. 1979 Nov;34(11):697-713.
4
Differentiation of bradykinin receptors and of kininases with conformational analogues of bradykinin.
Mol Pharmacol. 1978 May;14(3):413-21.
5
Analogs of bradykinin containing dehydrophenylalanine.
Adv Exp Med Biol. 1983;156:607-12.
6
D-Phe7-substituted peptide bradykinin antagonists are not substrates for kininase II.
Peptides. 1989 Jan-Feb;10(1):109-12. doi: 10.1016/0196-9781(89)90085-5.
7
[Phe8 psi(CH2-NH)Arg9]bradykinin, a B2 receptor selective agonist which is not broken down by either kininase I or kininase II.
Eur J Pharmacol. 1988 Oct 11;155(1-2):193-5. doi: 10.1016/0014-2999(88)90423-2.
8
Some characteristics of a peptidyl dipeptidase (kininase II) from rat CSF: differential effects of NaCl on the sequential degradation steps of bradykinin.
J Neurochem. 1990 Dec;55(6):1861-9. doi: 10.1111/j.1471-4159.1990.tb05769.x.
9
Pulmonary metabolism of bradykinin analogues and the contribution of angiotensin converting enzyme to bradykinin inactivation in isolated lungs.缓激肽类似物的肺代谢以及血管紧张素转换酶对离体肺中缓激肽失活的作用。
Br J Pharmacol. 1977 Jan;59(1):123-8. doi: 10.1111/j.1476-5381.1977.tb06985.x.
10
Metabolism of bradykinin in isolated perfused rat kidney. Measurement of kininase activity in perfusate and urine.
Adv Exp Med Biol. 1986;198 Pt A:367-73. doi: 10.1007/978-1-4684-5143-6_50.

本文引用的文献

1
Second kininase in human blood plasma.人血浆中的第二种激肽酶。
Nature. 1967 Sep 23;215(5108):1402-3. doi: 10.1038/2151402a0.
2
[Connection between structure and biological activity of new bradykinin analogs].[新型缓激肽类似物的结构与生物活性之间的联系]
Acta Biol Med Ger. 1974;33(1):77-88.
3
[Studies on bradykinin-binding cell fractions. 1. Characterization of kininase activity of the microsomal and membrane fraction from the rat uterus].[缓激肽结合细胞组分的研究。1. 大鼠子宫微粒体和膜组分激肽酶活性的特性]
Acta Biol Med Ger. 1975;34(1):9-13.