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Study on the chemical reactivity difference of primary hydroxyl groups in iridoid glycosides

Iridoid glycoside, which belongs to the polyhydroxy compound, is a kind of active ingredient of traditional Chinese medicine with a wide range of sources, and has many pharmacological effects such as anti-cancer, anti-inflammatory, anti-virus, hypoglycemic and so on. Its structure contains many hydr...

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Detalles Bibliográficos
Autores principales: Kong, Yuanfang, Xu, Jindan, Zhu, Pengbo, Wang, Shaopei, Yang, Bin, Zhang, Jingyu, Dong, Chunhong
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/PMC10637112/
https://www.ncbi.nlm.nih.gov/pubmed/37954426
http://dx.doi.org/10.1039/d3ra05674k
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author Kong, Yuanfang
Xu, Jindan
Zhu, Pengbo
Wang, Shaopei
Yang, Bin
Zhang, Jingyu
Dong, Chunhong
author_facet Kong, Yuanfang
Xu, Jindan
Zhu, Pengbo
Wang, Shaopei
Yang, Bin
Zhang, Jingyu
Dong, Chunhong
author_sort Kong, Yuanfang
collection PubMed
description Iridoid glycoside, which belongs to the polyhydroxy compound, is a kind of active ingredient of traditional Chinese medicine with a wide range of sources, and has many pharmacological effects such as anti-cancer, anti-inflammatory, anti-virus, hypoglycemic and so on. Its structure contains many hydroxyl groups, including two primary hydroxyl groups. The chemical reactivity of primary hydroxyl groups has very little difference, so it is very important to control the selectivity of hydroxyl groups under certain conditions. In this paper, the difference between the two primary hydroxyl groups in iridoid glycoside was calculated based on computer simulation and verified this result through designed experiments. This study will provide an important way for site-directed modification of hydroxyl in iridoid glycoside in the future.
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spelling pubmed-106371122023-11-11 Study on the chemical reactivity difference of primary hydroxyl groups in iridoid glycosides Kong, Yuanfang Xu, Jindan Zhu, Pengbo Wang, Shaopei Yang, Bin Zhang, Jingyu Dong, Chunhong RSC Adv Chemistry Iridoid glycoside, which belongs to the polyhydroxy compound, is a kind of active ingredient of traditional Chinese medicine with a wide range of sources, and has many pharmacological effects such as anti-cancer, anti-inflammatory, anti-virus, hypoglycemic and so on. Its structure contains many hydroxyl groups, including two primary hydroxyl groups. The chemical reactivity of primary hydroxyl groups has very little difference, so it is very important to control the selectivity of hydroxyl groups under certain conditions. In this paper, the difference between the two primary hydroxyl groups in iridoid glycoside was calculated based on computer simulation and verified this result through designed experiments. This study will provide an important way for site-directed modification of hydroxyl in iridoid glycoside in the future. The Royal Society of Chemistry 2023-11-10 /pmc/articles/PMC10637112/ /pubmed/37954426 http://dx.doi.org/10.1039/d3ra05674k Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Kong, Yuanfang
Xu, Jindan
Zhu, Pengbo
Wang, Shaopei
Yang, Bin
Zhang, Jingyu
Dong, Chunhong
Study on the chemical reactivity difference of primary hydroxyl groups in iridoid glycosides
title Study on the chemical reactivity difference of primary hydroxyl groups in iridoid glycosides
title_full Study on the chemical reactivity difference of primary hydroxyl groups in iridoid glycosides
title_fullStr Study on the chemical reactivity difference of primary hydroxyl groups in iridoid glycosides
title_full_unstemmed Study on the chemical reactivity difference of primary hydroxyl groups in iridoid glycosides
title_short Study on the chemical reactivity difference of primary hydroxyl groups in iridoid glycosides
title_sort study on the chemical reactivity difference of primary hydroxyl groups in iridoid glycosides
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10637112/
https://www.ncbi.nlm.nih.gov/pubmed/37954426
http://dx.doi.org/10.1039/d3ra05674k
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