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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2023
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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. |
format | Online Article Text |
id | pubmed-10472796 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
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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