• 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

Mechanism of inhibition of histidine decarboxylase by rhodanines.

作者信息

Free C A, Majchrowicz E, Hess S M

出版信息

Biochem Pharmacol. 1971 Jul;20(7):1421-8. doi: 10.1016/0006-2952(71)90269-3.

DOI:10.1016/0006-2952(71)90269-3
PMID:5163082
Abstract
摘要

相似文献

1
Mechanism of inhibition of histidine decarboxylase by rhodanines.罗丹宁对组氨酸脱羧酶的抑制机制
Biochem Pharmacol. 1971 Jul;20(7):1421-8. doi: 10.1016/0006-2952(71)90269-3.
2
The inhibition of histamine formation in vivo.体内组胺形成的抑制作用。
J Pharm Pharmacol. 1973 Aug;25(8):609-13. doi: 10.1111/j.2042-7158.1973.tb10646.x.
3
Inactivation of glutamate decarboxylase by bromopyruvate.
Biochem Biophys Res Commun. 1974 Jan 23;56(2):451-8. doi: 10.1016/0006-291x(74)90863-8.
4
Decarboxylase inhibition and structure-activity relationship studies with some newly synthetized benzyloxyamine and pyridylmethoxyamine derivatives.
Biochem Pharmacol. 1973 Sep 15;22(18):2267-75. doi: 10.1016/0006-2952(73)90007-5.
5
4-imidazolyl-3-amino-2-butanone (McN-A-1293), a new specific inhibitor of histidine decarboxylase.
Biochem Pharmacol. 1973 Sep 15;22(18):2299-310. doi: 10.1016/0006-2952(73)90011-7.
6
Inhibition of histidine decarboxylase and diamine oxidase by 4-bromo-3-hydroxybenzyloxyamine.4-溴-3-羟基苄氧胺对组氨酸脱羧酶和二胺氧化酶的抑制作用。
Biochem Pharmacol. 1970 May;19(5):1761-70. doi: 10.1016/0006-2952(70)90168-1.
7
Mechanism of inhibition of histidine decarboxylase (Clostridium welchii) by 4-bromo-3-hydroxybenzyloxamine and amino-oxyacetic acid.
Biochem Pharmacol. 1968 Dec;17(12):2498-501. doi: 10.1016/0006-2952(68)90145-7.
8
Mechanism of histidine decarboxylase inhibition by NSD-1055 and related hydroxylamines.NSD - 1055及相关羟胺对组氨酸脱羧酶的抑制机制。
Mol Pharmacol. 1968 Jul;4(4):337-48.
9
Inhibition of histidine decarboxylase. Derivatives of histidine.
J Med Chem. 1977 Apr;20(4):506-9. doi: 10.1021/jm00214a009.
10
Inhibition of histidine decarboxylases in vitro.
Arch Int Pharmacodyn Ther. 1972 Jan;195(1):109-47.

引用本文的文献

1
Rhodanine-3-acetamide derivatives as aldose and aldehyde reductase inhibitors to treat diabetic complications: synthesis, biological evaluation, molecular docking and simulation studies.罗丹宁-3-乙酰胺衍生物作为醛糖还原酶和醛还原酶抑制剂用于治疗糖尿病并发症：合成、生物学评价、分子对接及模拟研究
BMC Chem. 2021 Apr 27;15(1):28. doi: 10.1186/s13065-021-00756-z.
2
Cystathionine-β-Synthase: Molecular Regulation and Pharmacological Inhibition.胱硫醚-β-合酶：分子调控与药物抑制。
Biomolecules. 2020 Apr 30;10(5):697. doi: 10.3390/biom10050697.
3
Testing the ability of rhodanine and 2, 4-thiazolidinedione to interact with the human pancreatic alpha-amylase: electron-density descriptors complement molecular docking, QM, and QM/MM dynamics calculations.
检测若丹宁和2,4-噻唑烷二酮与人类胰腺α-淀粉酶相互作用的能力：电子密度描述符补充分子对接、量子力学和量子力学/分子力学动力学计算。
J Mol Model. 2017 Sep;23(9):252. doi: 10.1007/s00894-017-3418-5. Epub 2017 Aug 5.
4
Recent pharmacological developments on rhodanines and 2,4-thiazolidinediones.近期关于罗丹宁和2,4-噻唑烷二酮的药理学进展。
Int J Med Chem. 2013;2013:793260. doi: 10.1155/2013/793260. Epub 2013 May 2.
5
An efficient microwave assisted synthesis of novel class of Rhodanine derivatives as potential HIV-1 and JSP-1 inhibitors.一种高效微波辅助合成新型若丹宁衍生物作为潜在HIV-1和JSP-1抑制剂的方法。
Tetrahedron Lett. 2011 Aug 24;52(34):4375-4377. doi: 10.1016/j.tetlet.2011.05.114.
6
Mammalian histidine decarboxylase. Stability studies with special reference to the effect of salts.
Arch Dermatol Res. 1979 Nov;266(3):285-94. doi: 10.1007/BF00418574.
7
Peptide inhibition of mammalian histidine decarboxylase.
Agents Actions. 1979 Oct;9(4):314-8. doi: 10.1007/BF01970654.