Literature DB >> 6854583

Synthesis and antiarrhythmic and parasympatholytic properties of substituted phenols. 1. Heteroarylamine derivatives.

D M Stout, W L Matier, C Barcelon-Yang, R D Reynolds, B S Brown.   

Abstract

Twenty-four structural derivatives of the antiarrhythmic drug changrolin were synthesized and tested for antiarrhythmic and parasympatholytic activities. It was found that while the bis(pyrrolidinylmethyl)phenol pattern of changrolin appeared to be optimal in this series, a wide latitude existed for the heteroaryl substituent for maintaining good antiarrhythmic activity. Further, the antiarrhythmic and parasympatholytic activities tended to exhibit parallel changes.

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Year:  1983        PMID: 6854583     DOI: 10.1021/jm00360a005

Source DB:  PubMed          Journal:  J Med Chem        ISSN: 0022-2623            Impact factor:   7.446


  3 in total

1.  Comparison of the parasympatholytic activity of ACC-9358 and disopyramide.

Authors:  B S Brown; R J Gorczynski; R D Reynolds; J E Shaffer
Journal:  Br J Pharmacol       Date:  1986-01       Impact factor: 8.739

2.  Discovery of N-(3,5-bis(1-pyrrolidylmethyl)-4-hydroxybenzyl)-4-methoxybenzenesulfamide (sulcardine) as a novel anti-arrhythmic agent.

Authors:  Dong-Lu Bai; Wei-Zhou Chen; Yun-Xin Bo; Yue-Li Dong; Ai-Li Kang; Wei-Kang Sun; Wei Wang; Zhong-Liang Hu; Yi-Ping Wang
Journal:  Acta Pharmacol Sin       Date:  2012-08-27       Impact factor: 6.150

3.  Docking Studies of Methylthiomorpholin Phenols (LQM300 Series) with Angiotensin-Converting Enzyme (ACE).

Authors:  Víctor H Vázquez-Valadez; V H Abrego; Pablo A Martínez; Gabriela Torres; Oscar Zúñiga; Daniel Escutia; Rebeca Vilchis; Ana Ma Velázquez; Luisa Martínez; Mónica Ruiz; Brígida Camacho; Rafael López-Castañares; Enrique Angeles
Journal:  Open Med Chem J       Date:  2013-11-23
  3 in total

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