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Synthesis, Characterisation and Antitumour Activity of Some Quercetin Analogues

Quercetin is one of the most abundant naturally occurring flavonoid and is associated with a wide range of biological activities, such as antioxidant, antiinflammatory and anticancer activities. However, there are multiple problems associated with the bioavailability of quercetin, thereby restrictin...

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Autores principales: Gadhwal, M. K., Patil, Swati, D’Mello, Priscilla, Joshi, Urmila, Sinha, Ragini, Govil, G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3757866/
https://www.ncbi.nlm.nih.gov/pubmed/24019576
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author Gadhwal, M. K.
Patil, Swati
D’Mello, Priscilla
Joshi, Urmila
Sinha, Ragini
Govil, G.
author_facet Gadhwal, M. K.
Patil, Swati
D’Mello, Priscilla
Joshi, Urmila
Sinha, Ragini
Govil, G.
author_sort Gadhwal, M. K.
collection PubMed
description Quercetin is one of the most abundant naturally occurring flavonoid and is associated with a wide range of biological activities, such as antioxidant, antiinflammatory and anticancer activities. However, there are multiple problems associated with the bioavailability of quercetin, thereby restricting its use. Taking this into consideration, the structure of quercetin was modified by removal of multiple hydroxyl groups and introduction of substituents such as Cl, OCH(3) and N (CH(3))(2) on the p-position of the B-ring. The effect of structural modification on the anticancer activity was studied using four different cell lines, including MCF-7, HepG2, HCT-15 and PC-3. Compound 1a has shown an activity better than quercetin in HepG2 cell lines, whereas 1c and 1e showed significant growth inhibition of the HCT-15 cell lines.
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spelling pubmed-37578662013-09-09 Synthesis, Characterisation and Antitumour Activity of Some Quercetin Analogues Gadhwal, M. K. Patil, Swati D’Mello, Priscilla Joshi, Urmila Sinha, Ragini Govil, G. Indian J Pharm Sci Short Communications Quercetin is one of the most abundant naturally occurring flavonoid and is associated with a wide range of biological activities, such as antioxidant, antiinflammatory and anticancer activities. However, there are multiple problems associated with the bioavailability of quercetin, thereby restricting its use. Taking this into consideration, the structure of quercetin was modified by removal of multiple hydroxyl groups and introduction of substituents such as Cl, OCH(3) and N (CH(3))(2) on the p-position of the B-ring. The effect of structural modification on the anticancer activity was studied using four different cell lines, including MCF-7, HepG2, HCT-15 and PC-3. Compound 1a has shown an activity better than quercetin in HepG2 cell lines, whereas 1c and 1e showed significant growth inhibition of the HCT-15 cell lines. Medknow Publications & Media Pvt Ltd 2013 /pmc/articles/PMC3757866/ /pubmed/24019576 Text en Copyright: © Indian Journal of Pharmaceutical Sciences http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Communications
Gadhwal, M. K.
Patil, Swati
D’Mello, Priscilla
Joshi, Urmila
Sinha, Ragini
Govil, G.
Synthesis, Characterisation and Antitumour Activity of Some Quercetin Analogues
title Synthesis, Characterisation and Antitumour Activity of Some Quercetin Analogues
title_full Synthesis, Characterisation and Antitumour Activity of Some Quercetin Analogues
title_fullStr Synthesis, Characterisation and Antitumour Activity of Some Quercetin Analogues
title_full_unstemmed Synthesis, Characterisation and Antitumour Activity of Some Quercetin Analogues
title_short Synthesis, Characterisation and Antitumour Activity of Some Quercetin Analogues
title_sort synthesis, characterisation and antitumour activity of some quercetin analogues
topic Short Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3757866/
https://www.ncbi.nlm.nih.gov/pubmed/24019576
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