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1,2,3-三唑衍生物(一种有效的前列腺素合成体外抑制剂)的构效关系研究:杂环的作用

Structure-activity studies on a 1,2,3-triazole derivative, a potent in vitro inhibitor of prostaglandin synthesis: the role of the heterocyclic ring.

作者信息

Biagi G, Dell'Omodarme G, Ferretti M, Giorgi I, Livi O, Scartoni V

机构信息

Istituto di Chimica Farmaceutica e Tossicologica, Università di Pisa, Italy.

出版信息

Farmaco. 1992 Mar;47(3):335-44.

PMID:1503597
Abstract

This paper reports further structural modifications concerning the 1,2,3-triazole ring of the compound A, an effective in vitro inhibitor of prostaglandin synthesis. The introduction of different heterocyclic rings provided further information about of the role of the heterocyclic ring in enzymatic inhibition, as regards the number and position of the nitrogen atoms, the electronic effects, basicity, steric hindrance and hydrophilicity. The benzimidazole derivative 4e proved to possess a high enzymatic inhibitory activity.

摘要

本文报道了关于化合物A(一种有效的前列腺素合成体外抑制剂)的1,2,3 - 三唑环的进一步结构修饰。引入不同的杂环提供了关于杂环在酶抑制作用中作用的更多信息,涉及氮原子的数量和位置、电子效应、碱性、空间位阻和亲水性。苯并咪唑衍生物4e被证明具有高酶抑制活性。

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