Cargando…
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...
Autores principales: | , , , , , , , , , |
---|---|
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 |
_version_ | 1783699192353390592 |
---|---|
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. |
format | Online Article Text |
id | pubmed-8155391 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical
Society and American
Society of Pharmacognosy |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT vanzadelhoffannemiek towardasystematicnomenclatureforneolignanamides AT debruijnwouterjc towardasystematicnomenclatureforneolignanamides AT fangzhongxiang towardasystematicnomenclatureforneolignanamides AT gaquerelemmanuel towardasystematicnomenclatureforneolignanamides AT ishiharaatsushi towardasystematicnomenclatureforneolignanamides AT werckreichhartdaniele towardasystematicnomenclatureforneolignanamides AT zhangpangzhen towardasystematicnomenclatureforneolignanamides AT zhouguangxiong towardasystematicnomenclatureforneolignanamides AT franssenmauricecr towardasystematicnomenclatureforneolignanamides AT vinckenjeanpaul towardasystematicnomenclatureforneolignanamides |