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From Angiotensin II to Cyclic Peptides and Angiotensin Receptor Blockers (ARBs): Perspectives of ARBs in COVID-19 Therapy
- Source :
- Molecules, Molecules, Vol 26, Iss 618, p 618 (2021)
- Publication Year :
- 2021
- Publisher :
- MDPI AG, 2021.
-
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.
- Subjects :
- Sars-CoV-2
Pharmaceutical Science
Vasodilation
Review
030204 cardiovascular system & hematology
Pharmacology
Analytical Chemistry
lcsh:QD241-441
Renin-Angiotensin System
Angiotensin Receptor Antagonists
03 medical and health sciences
0302 clinical medicine
lcsh:Organic chemistry
Oral administration
Drug Discovery
Humans
Medicine
Physical and Theoretical Chemistry
030304 developmental biology
chemistry.chemical_classification
0303 health sciences
business.industry
Angiotensin II
Organic Chemistry
mimetics
Antagonist
COVID-19
cyclic peptides
sarmesin
Covid 19
sartans
Cyclic peptide
COVID-19 Drug Treatment
Losartan
chemistry
Chemistry (miscellaneous)
Hypertension
Molecular Medicine
transdermal delivery
business
Homeostasis
RAS
medicine.drug
Hormone
Subjects
Details
- ISSN :
- 14203049
- Volume :
- 26
- Database :
- OpenAIRE
- Journal :
- Molecules
- Accession number :
- edsair.doi.dedup.....19b8aa7ecd955d5e7e518f69508da5d4