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Chapter 3 Noniridoid Bisindole Alkaloids
This chapter discusses that indole is a reactive nucleus prone to dimerization when it is isolated or a part of tryptamine or tryptophan, which themselves are reactive toward many functionalities. For these reasons, bisindoles, the majority of which are of iridoid origin, are frequently isolated in...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Academic Press, Inc. Published by Elsevier Inc.
1995
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7148815/ http://dx.doi.org/10.1016/S0099-9598(08)60155-8 |
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author | Sapi, J. Massiot, G. |
author_facet | Sapi, J. Massiot, G. |
author_sort | Sapi, J. |
collection | PubMed |
description | This chapter discusses that indole is a reactive nucleus prone to dimerization when it is isolated or a part of tryptamine or tryptophan, which themselves are reactive toward many functionalities. For these reasons, bisindoles, the majority of which are of iridoid origin, are frequently isolated in nature. Besides these “dimers,” there exists a growing class of noniridoid bisindoles found in the marine environment, in microorganisms, and in plant species, many of which display interesting biological activities. The chapter tries to promote research on a series of compounds worthy of attention. Marine environments are a rich source of indole and bisindole alkaloids of great structural variety. In the absence of traditional use, the chemical constituents of marine organisms are separated following bioassay-guided fractionation, and, consequently, contrary to compounds from terrestrial sources, many of the structures are associated with significant biological activity. |
format | Online Article Text |
id | pubmed-7148815 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1995 |
publisher | Academic Press, Inc. Published by Elsevier Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71488152020-04-13 Chapter 3 Noniridoid Bisindole Alkaloids Sapi, J. Massiot, G. The Alkaloids. Chemistry and Physiology Article This chapter discusses that indole is a reactive nucleus prone to dimerization when it is isolated or a part of tryptamine or tryptophan, which themselves are reactive toward many functionalities. For these reasons, bisindoles, the majority of which are of iridoid origin, are frequently isolated in nature. Besides these “dimers,” there exists a growing class of noniridoid bisindoles found in the marine environment, in microorganisms, and in plant species, many of which display interesting biological activities. The chapter tries to promote research on a series of compounds worthy of attention. Marine environments are a rich source of indole and bisindole alkaloids of great structural variety. In the absence of traditional use, the chemical constituents of marine organisms are separated following bioassay-guided fractionation, and, consequently, contrary to compounds from terrestrial sources, many of the structures are associated with significant biological activity. Academic Press, Inc. Published by Elsevier Inc. 1995 2008-05-30 /pmc/articles/PMC7148815/ http://dx.doi.org/10.1016/S0099-9598(08)60155-8 Text en © 1995 Academic Press, Inc. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Sapi, J. Massiot, G. Chapter 3 Noniridoid Bisindole Alkaloids |
title | Chapter 3 Noniridoid Bisindole Alkaloids |
title_full | Chapter 3 Noniridoid Bisindole Alkaloids |
title_fullStr | Chapter 3 Noniridoid Bisindole Alkaloids |
title_full_unstemmed | Chapter 3 Noniridoid Bisindole Alkaloids |
title_short | Chapter 3 Noniridoid Bisindole Alkaloids |
title_sort | chapter 3 noniridoid bisindole alkaloids |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7148815/ http://dx.doi.org/10.1016/S0099-9598(08)60155-8 |
work_keys_str_mv | AT sapij chapter3noniridoidbisindolealkaloids AT massiotg chapter3noniridoidbisindolealkaloids |