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Progress in Studies on Rutaecarpine. II.—Synthesis and Structure-Biological Activity Relationships
Rutaecarpine is a pentacyclic indolopyridoquinazolinone alkaloid found in Evodia rutaecarpa and other related herbs. It has a variety of intriguing biological properties, which continue to attract the academic and industrial interest. Studies on rutaecarpine have included isolation from new natural...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272352/ https://www.ncbi.nlm.nih.gov/pubmed/26111170 http://dx.doi.org/10.3390/molecules200610800 |
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author | Son, Jong-Keun Chang, Hyeun Wook Jahng, Yurngdong |
author_facet | Son, Jong-Keun Chang, Hyeun Wook Jahng, Yurngdong |
author_sort | Son, Jong-Keun |
collection | PubMed |
description | Rutaecarpine is a pentacyclic indolopyridoquinazolinone alkaloid found in Evodia rutaecarpa and other related herbs. It has a variety of intriguing biological properties, which continue to attract the academic and industrial interest. Studies on rutaecarpine have included isolation from new natural sources, development of new synthetic methods for its total synthesis, the discovery of new biological activities, metabolism, toxicology, and establishment of analytical methods for determining rutaecarpine content. The present review focuses on the synthesis, biological activities, and structure-activity relationships of rutaecarpine derivatives, with respect to their antiplatelet, vasodilatory, cytotoxic, and anticholinesterase activities. |
format | Online Article Text |
id | pubmed-6272352 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62723522018-12-31 Progress in Studies on Rutaecarpine. II.—Synthesis and Structure-Biological Activity Relationships Son, Jong-Keun Chang, Hyeun Wook Jahng, Yurngdong Molecules Review Rutaecarpine is a pentacyclic indolopyridoquinazolinone alkaloid found in Evodia rutaecarpa and other related herbs. It has a variety of intriguing biological properties, which continue to attract the academic and industrial interest. Studies on rutaecarpine have included isolation from new natural sources, development of new synthetic methods for its total synthesis, the discovery of new biological activities, metabolism, toxicology, and establishment of analytical methods for determining rutaecarpine content. The present review focuses on the synthesis, biological activities, and structure-activity relationships of rutaecarpine derivatives, with respect to their antiplatelet, vasodilatory, cytotoxic, and anticholinesterase activities. MDPI 2015-06-11 /pmc/articles/PMC6272352/ /pubmed/26111170 http://dx.doi.org/10.3390/molecules200610800 Text en © 2015 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 license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Son, Jong-Keun Chang, Hyeun Wook Jahng, Yurngdong Progress in Studies on Rutaecarpine. II.—Synthesis and Structure-Biological Activity Relationships |
title | Progress in Studies on Rutaecarpine. II.—Synthesis and Structure-Biological Activity Relationships |
title_full | Progress in Studies on Rutaecarpine. II.—Synthesis and Structure-Biological Activity Relationships |
title_fullStr | Progress in Studies on Rutaecarpine. II.—Synthesis and Structure-Biological Activity Relationships |
title_full_unstemmed | Progress in Studies on Rutaecarpine. II.—Synthesis and Structure-Biological Activity Relationships |
title_short | Progress in Studies on Rutaecarpine. II.—Synthesis and Structure-Biological Activity Relationships |
title_sort | progress in studies on rutaecarpine. ii.—synthesis and structure-biological activity relationships |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272352/ https://www.ncbi.nlm.nih.gov/pubmed/26111170 http://dx.doi.org/10.3390/molecules200610800 |
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