Cargando…
Quinolizidine-Type Alkaloids: Chemodiversity, Occurrence, and Bioactivity
[Image: see text] Quinolizidine alkaloids (QAs) are nitrogen-containing compounds produced naturally as specialized metabolites distributed in plants and animals (e.g., frogs, sponges). The present review compiles the available information on the chemical diversity and biological activity of QAs rep...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10413377/ https://www.ncbi.nlm.nih.gov/pubmed/37576649 http://dx.doi.org/10.1021/acsomega.3c02179 |
_version_ | 1785087116446793728 |
---|---|
author | Cely-Veloza, Willy Kato, Massuo J. Coy-Barrera, Ericsson |
author_facet | Cely-Veloza, Willy Kato, Massuo J. Coy-Barrera, Ericsson |
author_sort | Cely-Veloza, Willy |
collection | PubMed |
description | [Image: see text] Quinolizidine alkaloids (QAs) are nitrogen-containing compounds produced naturally as specialized metabolites distributed in plants and animals (e.g., frogs, sponges). The present review compiles the available information on the chemical diversity and biological activity of QAs reported during the last three decades. So far, 397 QAs have been isolated, gathering 20 different representative classes, including the most common such as matrine (13.6%), lupanine (9.8%), anagyrine (4.0%), sparteine (5.3%), cytisine (6.5%), tetrahydrocytisine (4.3%), lupinine (12.1%), macrocyclic bisquinolizidine (9.3%), biphenylquinolizidine lactone (7.1%), dimeric (7.1%), and other less known QAs (20.9%), which include several structural patterns of QAs. A detailed survey of the reported information about the bioactivities of these compounds indicated their potential as cytotoxic, antiviral, antimicrobial, insecticidal, anti-inflammatory, antimalarial, and antiacetylcholinesterase compounds, involving favorable putative drug-likeness scores. In this regard, research progress on the structural and biological/pharmacological diversity of QAs requires further studies oriented on expanding the chemical space to find bioactive scaffolds based on QAs for pharmacological and agrochemical applications. |
format | Online Article Text |
id | pubmed-10413377 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-104133772023-08-11 Quinolizidine-Type Alkaloids: Chemodiversity, Occurrence, and Bioactivity Cely-Veloza, Willy Kato, Massuo J. Coy-Barrera, Ericsson ACS Omega [Image: see text] Quinolizidine alkaloids (QAs) are nitrogen-containing compounds produced naturally as specialized metabolites distributed in plants and animals (e.g., frogs, sponges). The present review compiles the available information on the chemical diversity and biological activity of QAs reported during the last three decades. So far, 397 QAs have been isolated, gathering 20 different representative classes, including the most common such as matrine (13.6%), lupanine (9.8%), anagyrine (4.0%), sparteine (5.3%), cytisine (6.5%), tetrahydrocytisine (4.3%), lupinine (12.1%), macrocyclic bisquinolizidine (9.3%), biphenylquinolizidine lactone (7.1%), dimeric (7.1%), and other less known QAs (20.9%), which include several structural patterns of QAs. A detailed survey of the reported information about the bioactivities of these compounds indicated their potential as cytotoxic, antiviral, antimicrobial, insecticidal, anti-inflammatory, antimalarial, and antiacetylcholinesterase compounds, involving favorable putative drug-likeness scores. In this regard, research progress on the structural and biological/pharmacological diversity of QAs requires further studies oriented on expanding the chemical space to find bioactive scaffolds based on QAs for pharmacological and agrochemical applications. American Chemical Society 2023-07-28 /pmc/articles/PMC10413377/ /pubmed/37576649 http://dx.doi.org/10.1021/acsomega.3c02179 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/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 | Cely-Veloza, Willy Kato, Massuo J. Coy-Barrera, Ericsson Quinolizidine-Type Alkaloids: Chemodiversity, Occurrence, and Bioactivity |
title | Quinolizidine-Type Alkaloids: Chemodiversity, Occurrence, and Bioactivity |
title_full | Quinolizidine-Type Alkaloids: Chemodiversity, Occurrence, and Bioactivity |
title_fullStr | Quinolizidine-Type Alkaloids: Chemodiversity, Occurrence, and Bioactivity |
title_full_unstemmed | Quinolizidine-Type Alkaloids: Chemodiversity, Occurrence, and Bioactivity |
title_short | Quinolizidine-Type Alkaloids: Chemodiversity, Occurrence, and Bioactivity |
title_sort | quinolizidine-type alkaloids: chemodiversity, occurrence, and bioactivity |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10413377/ https://www.ncbi.nlm.nih.gov/pubmed/37576649 http://dx.doi.org/10.1021/acsomega.3c02179 |
work_keys_str_mv | AT celyvelozawilly quinolizidinetypealkaloidschemodiversityoccurrenceandbioactivity AT katomassuoj quinolizidinetypealkaloidschemodiversityoccurrenceandbioactivity AT coybarreraericsson quinolizidinetypealkaloidschemodiversityoccurrenceandbioactivity |