2-Formylpyrrole natural products: origin, structural diversity, bioactivity and synthesis.


Journal

Natural product reports
ISSN: 1460-4752
Titre abrégé: Nat Prod Rep
Pays: England
ID NLM: 8502408

Informations de publication

Date de publication:
20 02 2019
Historique:
pubmed: 25 7 2018
medline: 9 8 2019
entrez: 25 7 2018
Statut: ppublish

Résumé

Covering: up to April 2018 2-Formylpyrroles are ubiquitous in nature, arising from the non-enzymatic Maillard reactions of amines and sugars. Often confused for secondary metabolites, these Maillard products display interesting biological activities including hepatoprotective, immunostimulatory, antiproliferative and antioxidant effects. This review presents all 2-formylpyrrole natural products reported to date and identifies structural sub-classes for their categorisation. The origin, biological activity and chemical syntheses of these natural products are discussed herein.

Identifiants

pubmed: 30039828
doi: 10.1039/c8np00051d
doi:

Substances chimiques

Alkaloids 0
Amino Sugars 0
Biogenic Amines 0
Biological Products 0
Pyrroles 0
funebral 105708-56-3

Types de publication

Journal Article Research Support, Non-U.S. Gov't Review

Langues

eng

Pagination

289-306

Auteurs

James M Wood (JM)

School of Chemical Sciences, University of Auckland, 23 Symonds St, Auckland, 1142, New Zealand. m.brimble@auckland.ac.nz.

Daniel P Furkert (DP)

School of Chemical Sciences, University of Auckland, 23 Symonds St, Auckland, 1142, New Zealand. m.brimble@auckland.ac.nz.

Margaret A Brimble (MA)

School of Chemical Sciences, University of Auckland, 23 Symonds St, Auckland, 1142, New Zealand. m.brimble@auckland.ac.nz and Maurice Wilkins Centre for Molecular Biodiscovery, University of Auckland, Private Bag 92019, Auckland 1142, New Zealand.

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Classifications MeSH