Structural Modification of Phenolic Acids: Modern Approaches to Synthesis and Study of Structure and Activity
Almagul K Umbetova1, Yuliya A Litvinenko1, Meruyert D Dauletova1
1Department of Chemistry and Technology of Organic Substances, Natural Compounds and Polymers, Faculty of Chemistry and Chemical Technology, Al-Farabi Kazakh National University, 71 Al-Farabi Ave., Almaty 050040, Kazakhstan.
None:
The paper discusses a comprehensive analysis of contemporary approaches to the structural modification of phenolic acids from the benzoic (C6-C1) and cinnamic (C6-C3) series, which have a wide range of biological activity. The main directions of chemical transformation of phenolic compounds that aim to improve their pharmaco-logical potential, stability, and bioavailability are discussed. The given study also makes an accent on the relationship between the structural features and biological effects of various phenolic acid derivatives, including antioxidant, anti-inflammatory, antimicrobial, and antitumor activity. The purpose of this investigation is to systematize current data on strategies for the structural modification of phenolic acids, to identify key areas of their chemical transformation, and to determine the most promising methods for creating biologically active compounds with improved pharmacological properties. The study was aimed at systematizing the accumulated knowledge and identifying promising areas for further research in the field of structural design of phenolic acid derivatives. Based on the analysis of experimental data and literature sources, key trends in the development of new medicinal compounds using the example of natural phenolic acids were characterized, and prospects for their use in medicine and pharmaceutical chemistry were shown.
More Related Videos
05:57Author Spotlight: In Silico Creation and Impact of Carbonylated Amino Acids on Protein Structure and Function
Published on: April 26, 2024
10:30A Generalized Method for Determining Free Soluble Phenolic Acid Composition and Antioxidant Capacity of Cereals and Legumes
Published on: June 10, 2022
Related Concept Videos
Structures of Carboxylic Acid Derivatives
Carboxylic acid derivatives contain an acyl group attached to a heteroatom such as chlorine, oxygen, or nitrogen. The carbonyl carbon and oxygen are both sp2-hybridized with an unhybridized p orbital.
The three sp2 orbitals of the carbonyl carbon form three σ bonds, one each with the carbonyl oxygen, the α carbon, and the heteroatom, whereas the other two sp2 orbitals of the carbonyl oxygen are occupied by the lone pairs. Further, the...
Adrenergic Agonists: Chemistry and Structure-Activity Relationship
Aromatic ring substitutions: Substituting the aromatic ring with –OH groups at positions 3 and 4 yields catecholamines (e.g., epinephrine), which have a high affinity for adrenoceptors. Hydrogen bonding between –OH groups and receptors enhances adrenergic activity.
Separation of...
Carboxylic Acid Derivatives: Overview
Structure and Nomenclature of Alcohols and Phenols
Alcohols are one of the most important functional groups in organic chemistry. The name of alcohol comes from the hydrocarbon from which it is derived. Alcohols are organic molecules containing the functional hydroxyl or –OH group directly bonded to carbon. Phenols have an OH group directly attached to a benzene ring. While alcohols are colorless, phenol is a white crystalline compound with a characteristic "hospital smell" odor.
As with other organic compounds, alcohols and...
Oxidation of Phenols to Quinones
o-hydroxy phenols are oxidized to o-quinones and p-hydroxy phenols to p-quinones. Such redox reactions involve the transfer of two electrons and two protons. The reversible redox...
Reactions of Carboxylic Acids: Introduction
