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Recent Advances in the Synthesis of β-Carboline Alkaloids
β-Carboline alkaloids are a remarkable family of natural and synthetic indole-containing heterocyclic compounds and they are widely distributed in nature. Recently, these alkaloids have been in the focus of interest, thanks to their diverse biological activities. Their pharmacological activity makes...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7866041/ https://www.ncbi.nlm.nih.gov/pubmed/33513936 http://dx.doi.org/10.3390/molecules26030663 |
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author | Szabó, Tímea Volk, Balázs Milen, Mátyás |
author_facet | Szabó, Tímea Volk, Balázs Milen, Mátyás |
author_sort | Szabó, Tímea |
collection | PubMed |
description | β-Carboline alkaloids are a remarkable family of natural and synthetic indole-containing heterocyclic compounds and they are widely distributed in nature. Recently, these alkaloids have been in the focus of interest, thanks to their diverse biological activities. Their pharmacological activity makes them desirable as sedative, anxiolytic, hypnotic, anticonvulsant, antitumor, antiviral, antiparasitic or antimicrobial drug candidates. The growing potential inherent in them encourages many researchers to address the challenges of the synthesis of natural products containing complex β-carboline frameworks. In this review, we describe the recent developments in the synthesis of β-carboline alkaloids and closely related derivatives through selected examples from the last 5 years. The focus is on the key steps with improved procedures and synthetic approaches. Furthermore the pharmacological potential of the alkaloids is also highlighted. |
format | Online Article Text |
id | pubmed-7866041 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-78660412021-02-07 Recent Advances in the Synthesis of β-Carboline Alkaloids Szabó, Tímea Volk, Balázs Milen, Mátyás Molecules Review β-Carboline alkaloids are a remarkable family of natural and synthetic indole-containing heterocyclic compounds and they are widely distributed in nature. Recently, these alkaloids have been in the focus of interest, thanks to their diverse biological activities. Their pharmacological activity makes them desirable as sedative, anxiolytic, hypnotic, anticonvulsant, antitumor, antiviral, antiparasitic or antimicrobial drug candidates. The growing potential inherent in them encourages many researchers to address the challenges of the synthesis of natural products containing complex β-carboline frameworks. In this review, we describe the recent developments in the synthesis of β-carboline alkaloids and closely related derivatives through selected examples from the last 5 years. The focus is on the key steps with improved procedures and synthetic approaches. Furthermore the pharmacological potential of the alkaloids is also highlighted. MDPI 2021-01-27 /pmc/articles/PMC7866041/ /pubmed/33513936 http://dx.doi.org/10.3390/molecules26030663 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Szabó, Tímea Volk, Balázs Milen, Mátyás Recent Advances in the Synthesis of β-Carboline Alkaloids |
title | Recent Advances in the Synthesis of β-Carboline Alkaloids |
title_full | Recent Advances in the Synthesis of β-Carboline Alkaloids |
title_fullStr | Recent Advances in the Synthesis of β-Carboline Alkaloids |
title_full_unstemmed | Recent Advances in the Synthesis of β-Carboline Alkaloids |
title_short | Recent Advances in the Synthesis of β-Carboline Alkaloids |
title_sort | recent advances in the synthesis of β-carboline alkaloids |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7866041/ https://www.ncbi.nlm.nih.gov/pubmed/33513936 http://dx.doi.org/10.3390/molecules26030663 |
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