J 2020

(Hetero)Aryloxyaminopropanols with N-Phenylpiperazine Structural Fragment - Review of Cardiovascular Activity

MARVANOVÁ, Pavlína, Tereza PADRTOVÁ and Petr MOKRÝ

Basic information

Original name

(Hetero)Aryloxyaminopropanols with N-Phenylpiperazine Structural Fragment - Review of Cardiovascular Activity

Authors

MARVANOVÁ, Pavlína (203 Czech Republic, guarantor, belonging to the institution), Tereza PADRTOVÁ (203 Czech Republic) and Petr MOKRÝ (203 Czech Republic)

Edition

Mini-reviews in medicinal chemistry, Sharjah, Betham Science Publ Ltd. 2020, 1389-5575

Other information

Language

English

Type of outcome

Článek v odborném periodiku

Field of Study

30104 Pharmacology and pharmacy

Country of publisher

United Arab Emirates

Confidentiality degree

není předmětem státního či obchodního tajemství

References:

URL

Impact factor

Impact factor: 3.862

RIV identification code

RIV/00216224:14160/20:00118111

Organization unit

Faculty of Pharmacy

DOI

http://dx.doi.org/10.2174/1389557520666200624192859

UT WoS

000591916700003

Keywords in English

Aryloxyphenylpiperazinylpropanols; cardiovascular system; chirality; connecting chain modification; N-phenylpiperazine; biological activities

Tags

rivok, ÚChL

Tags

International impact, Reviewed
Změněno: 24/2/2021 07:53, Mgr. Hana Hurtová

Abstract

V originále

Aryloxyphenylpiperazinylpropanols are a group of compounds exhibiting a wide range of biological activities, affecting the central nervous system and many cardiovascular mechanisms among them. As cardiovascular agents, aryloxyphenylpiperazinylpropanols work as antihypertensives, antiarrhythmics, cardiotonics or antiaggregants. The mechanism of action is almost always an alpha(1)-adrenolytic or combined alpha(1)- and beta-adrenolytic effect, but sometimes other mechanisms (e.g., Ca2+ antagonism or phosphodiesterase inhibition) can positively participate. In some cases, compounds with a small modification of the connecting chain also exhibit the desired cardiovascular effects. Several studies dealt with chirality of aryloxyphenylpiperazinylpropanols and determined the differences between the particular activities of racemic and enantiomeric compounds.
Displayed: 18/11/2024 17:16