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Natural 6-hydroxy-chromanols and -chromenols: structural diversity, biosynthetic pathways and health implications

We present the first comprehensive and systematic review on the structurally diverse toco-chromanols and -chromenols found in photosynthetic organisms, including marine organisms, and as metabolic intermediates in animals. The focus of this work is on the structural diversity of chromanols and chrom...

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Detalles Bibliográficos
Autores principales: Birringer, Marc, Siems, Karsten, Maxones, Alexander, Frank, Jan, Lorkowski, Stefan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9078042/
https://www.ncbi.nlm.nih.gov/pubmed/35539527
http://dx.doi.org/10.1039/c7ra11819h
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author Birringer, Marc
Siems, Karsten
Maxones, Alexander
Frank, Jan
Lorkowski, Stefan
author_facet Birringer, Marc
Siems, Karsten
Maxones, Alexander
Frank, Jan
Lorkowski, Stefan
author_sort Birringer, Marc
collection PubMed
description We present the first comprehensive and systematic review on the structurally diverse toco-chromanols and -chromenols found in photosynthetic organisms, including marine organisms, and as metabolic intermediates in animals. The focus of this work is on the structural diversity of chromanols and chromenols that result from various side chain modifications. We describe more than 230 structures that derive from a 6-hydroxy-chromanol- and 6-hydroxy-chromenol core, respectively, and comprise di-, sesqui-, mono- and hemiterpenes. We assort the compounds into a structure–activity relationship with special emphasis on anti-inflammatory and anti-carcinogenic activities of the congeners. This review covers the literature published from 1970 to 2017.
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spelling pubmed-90780422022-05-09 Natural 6-hydroxy-chromanols and -chromenols: structural diversity, biosynthetic pathways and health implications Birringer, Marc Siems, Karsten Maxones, Alexander Frank, Jan Lorkowski, Stefan RSC Adv Chemistry We present the first comprehensive and systematic review on the structurally diverse toco-chromanols and -chromenols found in photosynthetic organisms, including marine organisms, and as metabolic intermediates in animals. The focus of this work is on the structural diversity of chromanols and chromenols that result from various side chain modifications. We describe more than 230 structures that derive from a 6-hydroxy-chromanol- and 6-hydroxy-chromenol core, respectively, and comprise di-, sesqui-, mono- and hemiterpenes. We assort the compounds into a structure–activity relationship with special emphasis on anti-inflammatory and anti-carcinogenic activities of the congeners. This review covers the literature published from 1970 to 2017. The Royal Society of Chemistry 2018-01-26 /pmc/articles/PMC9078042/ /pubmed/35539527 http://dx.doi.org/10.1039/c7ra11819h Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Birringer, Marc
Siems, Karsten
Maxones, Alexander
Frank, Jan
Lorkowski, Stefan
Natural 6-hydroxy-chromanols and -chromenols: structural diversity, biosynthetic pathways and health implications
title Natural 6-hydroxy-chromanols and -chromenols: structural diversity, biosynthetic pathways and health implications
title_full Natural 6-hydroxy-chromanols and -chromenols: structural diversity, biosynthetic pathways and health implications
title_fullStr Natural 6-hydroxy-chromanols and -chromenols: structural diversity, biosynthetic pathways and health implications
title_full_unstemmed Natural 6-hydroxy-chromanols and -chromenols: structural diversity, biosynthetic pathways and health implications
title_short Natural 6-hydroxy-chromanols and -chromenols: structural diversity, biosynthetic pathways and health implications
title_sort natural 6-hydroxy-chromanols and -chromenols: structural diversity, biosynthetic pathways and health implications
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9078042/
https://www.ncbi.nlm.nih.gov/pubmed/35539527
http://dx.doi.org/10.1039/c7ra11819h
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