罗丹宁对组氨酸脱羧酶的抑制机制 - Suppr

Suppr

超能文献

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

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.

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.

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.

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.

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.

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.

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.

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.

Inhibition of histidine decarboxylase. Derivatives of histidine.

J Med Chem. 1977 Apr;20(4):506-9. doi: 10.1021/jm00214a009.

Inhibition of histidine decarboxylases in vitro.

Arch Int Pharmacodyn Ther. 1972 Jan;195(1):109-47.

引用本文的文献

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.

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.

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.

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.

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.

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.

Peptide inhibition of mammalian histidine decarboxylase.

Agents Actions. 1979 Oct;9(4):314-8. doi: 10.1007/BF01970654.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验