MARVANOVÁ, Pavlína, Tereza PADRTOVÁ and Petr MOKRÝ. (Hetero)Aryloxyaminopropanols with N-Phenylpiperazine Structural Fragment - Review of Cardiovascular Activity. Mini-reviews in medicinal chemistry. Sharjah: Betham Science Publ Ltd., 2020, vol. 20, No 17, p. 1719-1731. ISSN 1389-5575. Available from: https://dx.doi.org/10.2174/1389557520666200624192859.
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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
Original language English
Type of outcome Article in a journal
Field of Study 30104 Pharmacology and pharmacy
Country of publisher United Arab Emirates
Confidentiality degree is not subject to a state or trade secret
WWW 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
Changed by Changed by: Mgr. Hana Hurtová, učo 244985. Changed: 24/2/2021 07:53.
Abstract
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.
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