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Tanjungides A and B: New Antitumoral Bromoindole Derived Compounds from Diazona cf formosa. Isolation and Total Synthesis

Tanjungides A (1) (Z isomer) and B (2) (E isomer), two novel dibrominated indole enamides, have been isolated from the tunicate Diazona cf formosa. Their structures were determined by spectroscopic methods including HRMS, and extensive 1D and 2D NMR. The stereochemistry of the cyclised cystine prese...

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Autores principales: Murcia, Carmen, Coello, Laura, Fernández, Rogelio, Martín, María Jesús, Reyes, Fernando, Francesch, Andrés, Munt, Simon, Cuevas, Carmen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3944533/
https://www.ncbi.nlm.nih.gov/pubmed/24566261
http://dx.doi.org/10.3390/md12021116
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author Murcia, Carmen
Coello, Laura
Fernández, Rogelio
Martín, María Jesús
Reyes, Fernando
Francesch, Andrés
Munt, Simon
Cuevas, Carmen
author_facet Murcia, Carmen
Coello, Laura
Fernández, Rogelio
Martín, María Jesús
Reyes, Fernando
Francesch, Andrés
Munt, Simon
Cuevas, Carmen
author_sort Murcia, Carmen
collection PubMed
description Tanjungides A (1) (Z isomer) and B (2) (E isomer), two novel dibrominated indole enamides, have been isolated from the tunicate Diazona cf formosa. Their structures were determined by spectroscopic methods including HRMS, and extensive 1D and 2D NMR. The stereochemistry of the cyclised cystine present in both compounds was determined by Marfey’s analysis after chemical degradation and hydrolysis. We also report the first total synthesis of these compounds using methyl 1H-indole-3-carboxylate as starting material and a linear sequence of 11 chemical steps. Tanjungides A and B exhibit significant cytotoxicity against human tumor cell lines.
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spelling pubmed-39445332014-03-07 Tanjungides A and B: New Antitumoral Bromoindole Derived Compounds from Diazona cf formosa. Isolation and Total Synthesis Murcia, Carmen Coello, Laura Fernández, Rogelio Martín, María Jesús Reyes, Fernando Francesch, Andrés Munt, Simon Cuevas, Carmen Mar Drugs Tanjungides A (1) (Z isomer) and B (2) (E isomer), two novel dibrominated indole enamides, have been isolated from the tunicate Diazona cf formosa. Their structures were determined by spectroscopic methods including HRMS, and extensive 1D and 2D NMR. The stereochemistry of the cyclised cystine present in both compounds was determined by Marfey’s analysis after chemical degradation and hydrolysis. We also report the first total synthesis of these compounds using methyl 1H-indole-3-carboxylate as starting material and a linear sequence of 11 chemical steps. Tanjungides A and B exhibit significant cytotoxicity against human tumor cell lines. MDPI 2014-02-21 /pmc/articles/PMC3944533/ /pubmed/24566261 http://dx.doi.org/10.3390/md12021116 Text en © 2014 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/3.0/).
spellingShingle Murcia, Carmen
Coello, Laura
Fernández, Rogelio
Martín, María Jesús
Reyes, Fernando
Francesch, Andrés
Munt, Simon
Cuevas, Carmen
Tanjungides A and B: New Antitumoral Bromoindole Derived Compounds from Diazona cf formosa. Isolation and Total Synthesis
title Tanjungides A and B: New Antitumoral Bromoindole Derived Compounds from Diazona cf formosa. Isolation and Total Synthesis
title_full Tanjungides A and B: New Antitumoral Bromoindole Derived Compounds from Diazona cf formosa. Isolation and Total Synthesis
title_fullStr Tanjungides A and B: New Antitumoral Bromoindole Derived Compounds from Diazona cf formosa. Isolation and Total Synthesis
title_full_unstemmed Tanjungides A and B: New Antitumoral Bromoindole Derived Compounds from Diazona cf formosa. Isolation and Total Synthesis
title_short Tanjungides A and B: New Antitumoral Bromoindole Derived Compounds from Diazona cf formosa. Isolation and Total Synthesis
title_sort tanjungides a and b: new antitumoral bromoindole derived compounds from diazona cf formosa. isolation and total synthesis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3944533/
https://www.ncbi.nlm.nih.gov/pubmed/24566261
http://dx.doi.org/10.3390/md12021116
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