Antibacterial Effects of Flavonoids and Their Structure-Activity Relationship Study: A Comparative Interpretation

According to the latest report released by the World Health Organization, bacterial resistance to well-known and widely available antibacterial drugs has become a significant and severe global health concern and a grim challenge to tackle in order to cure infections associated with multidrug-resista...

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書目詳細資料
發表在:Molecules
主要作者: 2-s2.0-85125301964
格式: Review
語言:English
出版: MDPI 2022
在線閱讀:https://www.scopus.com/inward/record.uri?eid=2-s2.0-85125301964&doi=10.3390%2fmolecules27041149&partnerID=40&md5=2543e03b772340f8d75278659c82b63d
id Shamsudin N.F.; Ahmed Q.U.; Mahmood S.; Shah S.A.A.; Khatib A.; Mukhtar S.; Alsharif M.A.; Parveen H.; Zakaria Z.A.
spelling Shamsudin N.F.; Ahmed Q.U.; Mahmood S.; Shah S.A.A.; Khatib A.; Mukhtar S.; Alsharif M.A.; Parveen H.; Zakaria Z.A.
2-s2.0-85125301964
Antibacterial Effects of Flavonoids and Their Structure-Activity Relationship Study: A Comparative Interpretation
2022
Molecules
27
4
10.3390/molecules27041149
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85125301964&doi=10.3390%2fmolecules27041149&partnerID=40&md5=2543e03b772340f8d75278659c82b63d
According to the latest report released by the World Health Organization, bacterial resistance to well-known and widely available antibacterial drugs has become a significant and severe global health concern and a grim challenge to tackle in order to cure infections associated with multidrug-resistant pathogenic microorganisms efficiently. Consequently, various strategies have been orchestrated to cure the severe complications related to multidrug-resistant bacteria effectively. Some approaches involved the retardation of biofilm formation and multidrug-resistance pumps in bacteria as well as the discovery of new antimicrobial agents demonstrating different mechanisms of action. In this regard, natural products namely alkaloids, terpenoids, steroids, anthraquinone, flavonoids, saponins, tannins, etc., have been suggested to tackle the multidrug-resistant bacterial strains owing to their versatile pharmacological effects. Amongst these, flavonoids, also known as polyphenolic compounds, have been widely evaluated for their antibacterial property due to their tendency to retard the growth of a wide range of pathogenic microorganisms, including multidrug-resistant bacteria. The hydroxylation of C5, C7, C3′, and C4′; and geranylation or prenylation at C6 have been extensively studied to increase bacterial inhibition of flavonoids. On the other hand, methoxylation at C3′ and C5 has been reported to decrease flavonoids’ antibacterial action. Hence, the latest information on the antibacterial activity of flavonoids is summarized in this review, with particular attention to the structure-activity relationship of this broad class of natural compounds to discover safe and potent antibacterial agents as natural products. © 2022 by the authors. Licensee MDPI, Basel, Switzerland.
MDPI
14203049
English
Review
All Open Access; Gold Open Access; Green Open Access
author 2-s2.0-85125301964
spellingShingle 2-s2.0-85125301964
Antibacterial Effects of Flavonoids and Their Structure-Activity Relationship Study: A Comparative Interpretation
author_facet 2-s2.0-85125301964
author_sort 2-s2.0-85125301964
title Antibacterial Effects of Flavonoids and Their Structure-Activity Relationship Study: A Comparative Interpretation
title_short Antibacterial Effects of Flavonoids and Their Structure-Activity Relationship Study: A Comparative Interpretation
title_full Antibacterial Effects of Flavonoids and Their Structure-Activity Relationship Study: A Comparative Interpretation
title_fullStr Antibacterial Effects of Flavonoids and Their Structure-Activity Relationship Study: A Comparative Interpretation
title_full_unstemmed Antibacterial Effects of Flavonoids and Their Structure-Activity Relationship Study: A Comparative Interpretation
title_sort Antibacterial Effects of Flavonoids and Their Structure-Activity Relationship Study: A Comparative Interpretation
publishDate 2022
container_title Molecules
container_volume 27
container_issue 4
doi_str_mv 10.3390/molecules27041149
url https://www.scopus.com/inward/record.uri?eid=2-s2.0-85125301964&doi=10.3390%2fmolecules27041149&partnerID=40&md5=2543e03b772340f8d75278659c82b63d
description According to the latest report released by the World Health Organization, bacterial resistance to well-known and widely available antibacterial drugs has become a significant and severe global health concern and a grim challenge to tackle in order to cure infections associated with multidrug-resistant pathogenic microorganisms efficiently. Consequently, various strategies have been orchestrated to cure the severe complications related to multidrug-resistant bacteria effectively. Some approaches involved the retardation of biofilm formation and multidrug-resistance pumps in bacteria as well as the discovery of new antimicrobial agents demonstrating different mechanisms of action. In this regard, natural products namely alkaloids, terpenoids, steroids, anthraquinone, flavonoids, saponins, tannins, etc., have been suggested to tackle the multidrug-resistant bacterial strains owing to their versatile pharmacological effects. Amongst these, flavonoids, also known as polyphenolic compounds, have been widely evaluated for their antibacterial property due to their tendency to retard the growth of a wide range of pathogenic microorganisms, including multidrug-resistant bacteria. The hydroxylation of C5, C7, C3′, and C4′; and geranylation or prenylation at C6 have been extensively studied to increase bacterial inhibition of flavonoids. On the other hand, methoxylation at C3′ and C5 has been reported to decrease flavonoids’ antibacterial action. Hence, the latest information on the antibacterial activity of flavonoids is summarized in this review, with particular attention to the structure-activity relationship of this broad class of natural compounds to discover safe and potent antibacterial agents as natural products. © 2022 by the authors. Licensee MDPI, Basel, Switzerland.
publisher MDPI
issn 14203049
language English
format Review
accesstype All Open Access; Gold Open Access; Green Open Access
record_format scopus
collection Scopus
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