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Isolation and synthesis of cryptosanguinolentine (isocryptolepine), a naturally-occurring bioactive indoloquinoline alkaloid

Cryptosanguinolentine (isocryptolepine) is one of the minor naturally-occurring monomeric indoloquinoline alkaloids, isolated from the West African climbing shrub Cryptolepis sanguinolenta. The natural product displays such a simple and unique skeleton, which chemists became interested in well befor...

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Autores principales: Thobokholt, Elida N., Larghi, Enrique L., Bracca, Andrea B. J., Kaufman, Teodoro S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9054090/
https://www.ncbi.nlm.nih.gov/pubmed/35518305
http://dx.doi.org/10.1039/d0ra03096a
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author Thobokholt, Elida N.
Larghi, Enrique L.
Bracca, Andrea B. J.
Kaufman, Teodoro S.
author_facet Thobokholt, Elida N.
Larghi, Enrique L.
Bracca, Andrea B. J.
Kaufman, Teodoro S.
author_sort Thobokholt, Elida N.
collection PubMed
description Cryptosanguinolentine (isocryptolepine) is one of the minor naturally-occurring monomeric indoloquinoline alkaloids, isolated from the West African climbing shrub Cryptolepis sanguinolenta. The natural product displays such a simple and unique skeleton, which chemists became interested in well before it was found in Nature. Because of its structure and biological activity, the natural product has been targeted for synthesis on numerous occasions, employing a wide range of different strategies. Hence, discussed here are aspects related to the isolation of isocryptolepine, as well as the various approaches toward its total synthesis.
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spelling pubmed-90540902022-05-04 Isolation and synthesis of cryptosanguinolentine (isocryptolepine), a naturally-occurring bioactive indoloquinoline alkaloid Thobokholt, Elida N. Larghi, Enrique L. Bracca, Andrea B. J. Kaufman, Teodoro S. RSC Adv Chemistry Cryptosanguinolentine (isocryptolepine) is one of the minor naturally-occurring monomeric indoloquinoline alkaloids, isolated from the West African climbing shrub Cryptolepis sanguinolenta. The natural product displays such a simple and unique skeleton, which chemists became interested in well before it was found in Nature. Because of its structure and biological activity, the natural product has been targeted for synthesis on numerous occasions, employing a wide range of different strategies. Hence, discussed here are aspects related to the isolation of isocryptolepine, as well as the various approaches toward its total synthesis. The Royal Society of Chemistry 2020-05-19 /pmc/articles/PMC9054090/ /pubmed/35518305 http://dx.doi.org/10.1039/d0ra03096a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Thobokholt, Elida N.
Larghi, Enrique L.
Bracca, Andrea B. J.
Kaufman, Teodoro S.
Isolation and synthesis of cryptosanguinolentine (isocryptolepine), a naturally-occurring bioactive indoloquinoline alkaloid
title Isolation and synthesis of cryptosanguinolentine (isocryptolepine), a naturally-occurring bioactive indoloquinoline alkaloid
title_full Isolation and synthesis of cryptosanguinolentine (isocryptolepine), a naturally-occurring bioactive indoloquinoline alkaloid
title_fullStr Isolation and synthesis of cryptosanguinolentine (isocryptolepine), a naturally-occurring bioactive indoloquinoline alkaloid
title_full_unstemmed Isolation and synthesis of cryptosanguinolentine (isocryptolepine), a naturally-occurring bioactive indoloquinoline alkaloid
title_short Isolation and synthesis of cryptosanguinolentine (isocryptolepine), a naturally-occurring bioactive indoloquinoline alkaloid
title_sort isolation and synthesis of cryptosanguinolentine (isocryptolepine), a naturally-occurring bioactive indoloquinoline alkaloid
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9054090/
https://www.ncbi.nlm.nih.gov/pubmed/35518305
http://dx.doi.org/10.1039/d0ra03096a
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