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Toward a Systematic Nomenclature for (Neo)Lignanamides

[Image: see text] Phenylalkenoic acid amides, often referred to as phenol amides or hydroxycinnamic acid amides, are bioactive phytochemicals, whose bioactivity can be enhanced by coupling to form dimers or oligomers. Phenylalkenoic acid amides consist of a (hydroxy)cinnamic acid derivative (i.e., t...

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Autores principales: van Zadelhoff, Annemiek, de Bruijn, Wouter J. C., Fang, Zhongxiang, Gaquerel, Emmanuel, Ishihara, Atsushi, Werck-Reichhart, Danièle, Zhang, Pangzhen, Zhou, Guangxiong, Franssen, Maurice C. R., Vincken, Jean-Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society and American Society of Pharmacognosy 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8155391/
https://www.ncbi.nlm.nih.gov/pubmed/33787264
http://dx.doi.org/10.1021/acs.jnatprod.0c00792
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author van Zadelhoff, Annemiek
de Bruijn, Wouter J. C.
Fang, Zhongxiang
Gaquerel, Emmanuel
Ishihara, Atsushi
Werck-Reichhart, Danièle
Zhang, Pangzhen
Zhou, Guangxiong
Franssen, Maurice C. R.
Vincken, Jean-Paul
author_facet van Zadelhoff, Annemiek
de Bruijn, Wouter J. C.
Fang, Zhongxiang
Gaquerel, Emmanuel
Ishihara, Atsushi
Werck-Reichhart, Danièle
Zhang, Pangzhen
Zhou, Guangxiong
Franssen, Maurice C. R.
Vincken, Jean-Paul
author_sort van Zadelhoff, Annemiek
collection PubMed
description [Image: see text] Phenylalkenoic acid amides, often referred to as phenol amides or hydroxycinnamic acid amides, are bioactive phytochemicals, whose bioactivity can be enhanced by coupling to form dimers or oligomers. Phenylalkenoic acid amides consist of a (hydroxy)cinnamic acid derivative (i.e., the phenylalkenoic acid subunit) linked to an amine-containing compound (i.e., the amine subunit) via an amide bond. The phenylalkenoic acid moiety can undergo oxidative coupling, either catalyzed by oxidative enzymes or due to autoxidation, which leads to the formation of (neo)lignanamides. Dimers described in the literature are often named after the species in which the compound was first discovered; however, the naming of these compounds lacks a systematic approach. We propose a new nomenclature, inspired by the existing system used for hydroxycinnamic acid dimers and lignin. In the proposed systematic nomenclature for (neo)lignanamides, compound names will be composed of three-letter codes and prefixes denoting the subunits, and numbers that indicate the carbon atoms involved in the linkage between the monomeric precursors. The proposed nomenclature is consistent, future-proof, and systematic.
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spelling pubmed-81553912021-05-28 Toward a Systematic Nomenclature for (Neo)Lignanamides van Zadelhoff, Annemiek de Bruijn, Wouter J. C. Fang, Zhongxiang Gaquerel, Emmanuel Ishihara, Atsushi Werck-Reichhart, Danièle Zhang, Pangzhen Zhou, Guangxiong Franssen, Maurice C. R. Vincken, Jean-Paul J Nat Prod [Image: see text] Phenylalkenoic acid amides, often referred to as phenol amides or hydroxycinnamic acid amides, are bioactive phytochemicals, whose bioactivity can be enhanced by coupling to form dimers or oligomers. Phenylalkenoic acid amides consist of a (hydroxy)cinnamic acid derivative (i.e., the phenylalkenoic acid subunit) linked to an amine-containing compound (i.e., the amine subunit) via an amide bond. The phenylalkenoic acid moiety can undergo oxidative coupling, either catalyzed by oxidative enzymes or due to autoxidation, which leads to the formation of (neo)lignanamides. Dimers described in the literature are often named after the species in which the compound was first discovered; however, the naming of these compounds lacks a systematic approach. We propose a new nomenclature, inspired by the existing system used for hydroxycinnamic acid dimers and lignin. In the proposed systematic nomenclature for (neo)lignanamides, compound names will be composed of three-letter codes and prefixes denoting the subunits, and numbers that indicate the carbon atoms involved in the linkage between the monomeric precursors. The proposed nomenclature is consistent, future-proof, and systematic. American Chemical Society and American Society of Pharmacognosy 2021-03-31 2021-04-23 /pmc/articles/PMC8155391/ /pubmed/33787264 http://dx.doi.org/10.1021/acs.jnatprod.0c00792 Text en © 2021 American Chemical Society Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle van Zadelhoff, Annemiek
de Bruijn, Wouter J. C.
Fang, Zhongxiang
Gaquerel, Emmanuel
Ishihara, Atsushi
Werck-Reichhart, Danièle
Zhang, Pangzhen
Zhou, Guangxiong
Franssen, Maurice C. R.
Vincken, Jean-Paul
Toward a Systematic Nomenclature for (Neo)Lignanamides
title Toward a Systematic Nomenclature for (Neo)Lignanamides
title_full Toward a Systematic Nomenclature for (Neo)Lignanamides
title_fullStr Toward a Systematic Nomenclature for (Neo)Lignanamides
title_full_unstemmed Toward a Systematic Nomenclature for (Neo)Lignanamides
title_short Toward a Systematic Nomenclature for (Neo)Lignanamides
title_sort toward a systematic nomenclature for (neo)lignanamides
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8155391/
https://www.ncbi.nlm.nih.gov/pubmed/33787264
http://dx.doi.org/10.1021/acs.jnatprod.0c00792
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