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A concise synthesis route to access bioactive natural products-dihydrocurcumins/1,7-diarylheptanoids

Dihydrocurcumin (DHCUR), a natural product and reductive metabolite of curcumin (CUR), is limitedly explored owing to its low bioavailability and limited accessibility due to lack of straightforward synthetic routes and poor yields with known methods. Herein, we report a concise and straightforward...

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Detalles Bibliográficos
Autores principales: Tripathi, Datendra Nath, Rajendran, Saravanakumar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10472796/
https://www.ncbi.nlm.nih.gov/pubmed/37664191
http://dx.doi.org/10.1039/d3ra05049a
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author Tripathi, Datendra Nath
Rajendran, Saravanakumar
author_facet Tripathi, Datendra Nath
Rajendran, Saravanakumar
author_sort Tripathi, Datendra Nath
collection PubMed
description Dihydrocurcumin (DHCUR), a natural product and reductive metabolite of curcumin (CUR), is limitedly explored owing to its low bioavailability and limited accessibility due to lack of straightforward synthetic routes and poor yields with known methods. Herein, we report a concise and straightforward route to synthesize DHCUR and its analogs in excellent yields. Dihydroferuloylacetone is condensed with aldehydes to obtain desired DHCURs/1,7-diarylheptanoids in 81–90% yields. The developed protocol facilitates easy access to bioactive natural products, 1,7-diarylheptanoids and DHCUR, for therapeutic study.
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spelling pubmed-104727962023-09-02 A concise synthesis route to access bioactive natural products-dihydrocurcumins/1,7-diarylheptanoids Tripathi, Datendra Nath Rajendran, Saravanakumar RSC Adv Chemistry Dihydrocurcumin (DHCUR), a natural product and reductive metabolite of curcumin (CUR), is limitedly explored owing to its low bioavailability and limited accessibility due to lack of straightforward synthetic routes and poor yields with known methods. Herein, we report a concise and straightforward route to synthesize DHCUR and its analogs in excellent yields. Dihydroferuloylacetone is condensed with aldehydes to obtain desired DHCURs/1,7-diarylheptanoids in 81–90% yields. The developed protocol facilitates easy access to bioactive natural products, 1,7-diarylheptanoids and DHCUR, for therapeutic study. The Royal Society of Chemistry 2023-09-01 /pmc/articles/PMC10472796/ /pubmed/37664191 http://dx.doi.org/10.1039/d3ra05049a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Tripathi, Datendra Nath
Rajendran, Saravanakumar
A concise synthesis route to access bioactive natural products-dihydrocurcumins/1,7-diarylheptanoids
title A concise synthesis route to access bioactive natural products-dihydrocurcumins/1,7-diarylheptanoids
title_full A concise synthesis route to access bioactive natural products-dihydrocurcumins/1,7-diarylheptanoids
title_fullStr A concise synthesis route to access bioactive natural products-dihydrocurcumins/1,7-diarylheptanoids
title_full_unstemmed A concise synthesis route to access bioactive natural products-dihydrocurcumins/1,7-diarylheptanoids
title_short A concise synthesis route to access bioactive natural products-dihydrocurcumins/1,7-diarylheptanoids
title_sort concise synthesis route to access bioactive natural products-dihydrocurcumins/1,7-diarylheptanoids
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10472796/
https://www.ncbi.nlm.nih.gov/pubmed/37664191
http://dx.doi.org/10.1039/d3ra05049a
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