| Literature DB >> 33504092 |
John Matsoukas1,2,3, Vasso Apostolopoulos1, Anthony Zulli1, Graham Moore4, Konstantinos Kelaidonis3, Kalliopi Moschovou5, Thomas Mavromoustakos5.
Abstract
The octapeptide hormone angiotensin II is one of the most studied peptides with the aim of designing and synthesizing non-peptide mimetics for oral administration. To achieve this, cyclizations at different positions within the peptide molecule has been a useful strategy to define the active conformation. These studies on angiotensin II led to the discovery of Sarmesin, a type II angiotensin II antagonist, and the breakthrough non-peptide mimetic Losartan, the first in a series of sartans marketed as a new generation of anti-hypertensive drugs in the 1990s. Angiotensin II receptor blockers (ARBS) and angiotensin I converting enzyme inhibitors (ACEI) were recently reported to protect hypertensive patients infected with SARS-CoV-2. The renin-angiotensin system (RAS) inhibitors reduce excess angiotensin II and increase antagonist heptapeptides alamandine and aspamandine which counterbalance angiotensin II and maintain homeostasis and vasodilation.Entities:
Keywords: Covid 19; RAS; Sarmesin; Sars-CoV-2; Sartans; angiotensin II; cyclic peptides; mimetics; transdermal delivery
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Year: 2021 PMID: 33504092 PMCID: PMC7865783 DOI: 10.3390/molecules26030618
Source DB: PubMed Journal: Molecules ISSN: 1420-3049 Impact factor: 4.411