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Advances in Research on Semi-Synthesis, Biotransformation and Biological Activities of Novel Derivatives from Maslinic Acid.

Authors :
Trabelsi, Yosra
Znati, Mansour
Ben Jannet, Hichem
Bouajila, Jalloul
Source :
Chemistry (2624-8549). Oct2024, Vol. 6 Issue 5, p1146-1188. 43p.
Publication Year :
2024

Abstract

Since ancient times, humans have turned to medicinal plants for treating various ailments and curing specific diseases, as these natural plants serve as the primary source of a range of phytochemicals, including triterpenes. Maslinic acid (MA), also known as (2α,3β)-2,3-dihydroxyolean-12-en-28-oic acid, is a pentacyclic triterpene acid present in numerous plants including olive, known for its high safety profile in humans. Recent experimental data increasingly suggests that MA exhibits diverse biological properties and therapeutic effects on various organ diseases, highlighting its significant potential for clinical applications due to its diverse potential pharmacological activities that promote health and resist various diseases, such as hypoglycemic, neuroprotective, anti-tumor, anti-inflammatory, antioxidant and multiple other biological activities. However, the undesirable pharmacokinetic properties of MA, such as high lipophilicity, pose a limitation to its application and development, impacting its bioavailability. Consequently, extensive research spanning decades has focused on structurally modifying MA to overcome these limitations and enhance its pharmacokinetic and therapeutic characteristics, leading to the identification of several potential lead compounds. In this review, we focus on the progress of research in recent years on MA with interest to its chemical and enzymatic modifications as well as the relationships between the modified structures or derivatives and their biological activities. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
26248549
Volume :
6
Issue :
5
Database :
Academic Search Index
Journal :
Chemistry (2624-8549)
Publication Type :
Academic Journal
Accession number :
180556372
Full Text :
https://doi.org/10.3390/chemistry6050067