| Literature DB >> 33787264 |
Annemiek van Zadelhoff1, Wouter J C de Bruijn1, Zhongxiang Fang2, Emmanuel Gaquerel3, Atsushi Ishihara4, Danièle Werck-Reichhart3, Pangzhen Zhang2, Guangxiong Zhou5, Maurice C R Franssen6, Jean-Paul Vincken1.
Abstract
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.Entities:
Year: 2021 PMID: 33787264 DOI: 10.1021/acs.jnatprod.0c00792
Source DB: PubMed Journal: J Nat Prod ISSN: 0163-3864 Impact factor: 4.050