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Chalcones: Synthetic Chemistry Follows Where Nature Leads
Chalcones belong to the flavonoid class of phenolic compounds. They form one of the largest groups of bioactive natural products. The potential anticancer, anti-inflammatory, antimicrobial, antioxidant, and antiparasitic properties of naturally occurring chalcones, and their unique chemical structur...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8392591/ https://www.ncbi.nlm.nih.gov/pubmed/34439870 http://dx.doi.org/10.3390/biom11081203 |
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author | Jasim, Hiba A. Nahar, Lutfun Jasim, Mohammad A. Moore, Sharon A. Ritchie, Kenneth J. Sarker, Satyajit D. |
author_facet | Jasim, Hiba A. Nahar, Lutfun Jasim, Mohammad A. Moore, Sharon A. Ritchie, Kenneth J. Sarker, Satyajit D. |
author_sort | Jasim, Hiba A. |
collection | PubMed |
description | Chalcones belong to the flavonoid class of phenolic compounds. They form one of the largest groups of bioactive natural products. The potential anticancer, anti-inflammatory, antimicrobial, antioxidant, and antiparasitic properties of naturally occurring chalcones, and their unique chemical structural features inspired the synthesis of numerous chalcone derivatives. In fact, structural features of chalcones are easy to construct from simple aromatic compounds, and it is convenient to perform structural modifications to generate functionalized chalcone derivatives. Many of these synthetic analogs were shown to possess similar bioactivities as their natural counterparts, but often with an enhanced potency and reduced toxicity. This review article aims to demonstrate how bioinspired synthesis of chalcone derivatives can potentially introduce a new chemical space for exploitation for new drug discovery, justifying the title of this article. However, the focus remains on critical appraisal of synthesized chalcones and their derivatives for their bioactivities, linking to their interactions at the biomolecular level where appropriate, and revealing their possible mechanisms of action. |
format | Online Article Text |
id | pubmed-8392591 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-83925912021-08-28 Chalcones: Synthetic Chemistry Follows Where Nature Leads Jasim, Hiba A. Nahar, Lutfun Jasim, Mohammad A. Moore, Sharon A. Ritchie, Kenneth J. Sarker, Satyajit D. Biomolecules Review Chalcones belong to the flavonoid class of phenolic compounds. They form one of the largest groups of bioactive natural products. The potential anticancer, anti-inflammatory, antimicrobial, antioxidant, and antiparasitic properties of naturally occurring chalcones, and their unique chemical structural features inspired the synthesis of numerous chalcone derivatives. In fact, structural features of chalcones are easy to construct from simple aromatic compounds, and it is convenient to perform structural modifications to generate functionalized chalcone derivatives. Many of these synthetic analogs were shown to possess similar bioactivities as their natural counterparts, but often with an enhanced potency and reduced toxicity. This review article aims to demonstrate how bioinspired synthesis of chalcone derivatives can potentially introduce a new chemical space for exploitation for new drug discovery, justifying the title of this article. However, the focus remains on critical appraisal of synthesized chalcones and their derivatives for their bioactivities, linking to their interactions at the biomolecular level where appropriate, and revealing their possible mechanisms of action. MDPI 2021-08-13 /pmc/articles/PMC8392591/ /pubmed/34439870 http://dx.doi.org/10.3390/biom11081203 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Jasim, Hiba A. Nahar, Lutfun Jasim, Mohammad A. Moore, Sharon A. Ritchie, Kenneth J. Sarker, Satyajit D. Chalcones: Synthetic Chemistry Follows Where Nature Leads |
title | Chalcones: Synthetic Chemistry Follows Where Nature Leads |
title_full | Chalcones: Synthetic Chemistry Follows Where Nature Leads |
title_fullStr | Chalcones: Synthetic Chemistry Follows Where Nature Leads |
title_full_unstemmed | Chalcones: Synthetic Chemistry Follows Where Nature Leads |
title_short | Chalcones: Synthetic Chemistry Follows Where Nature Leads |
title_sort | chalcones: synthetic chemistry follows where nature leads |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8392591/ https://www.ncbi.nlm.nih.gov/pubmed/34439870 http://dx.doi.org/10.3390/biom11081203 |
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