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Synthesis and Bioactivity of Luffarin I
The first synthesis of Luffarin I, sesterterpenolide isolated from sponge Luffariella geometrica, has been accomplished from commercially available sclareol. The key strategy involved in this synthesis is the diastereoselective reduction of an intermediate ketone. Luffarin I against human solid tumo...
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/PMC4413218/ https://www.ncbi.nlm.nih.gov/pubmed/25903281 http://dx.doi.org/10.3390/md13042407 |
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author | Urosa, Aitor Marcos, Isidro S. Díez, David Lithgow, Anna Plata, Gabriela B. Padrón, José M. Basabe, Pilar |
author_facet | Urosa, Aitor Marcos, Isidro S. Díez, David Lithgow, Anna Plata, Gabriela B. Padrón, José M. Basabe, Pilar |
author_sort | Urosa, Aitor |
collection | PubMed |
description | The first synthesis of Luffarin I, sesterterpenolide isolated from sponge Luffariella geometrica, has been accomplished from commercially available sclareol. The key strategy involved in this synthesis is the diastereoselective reduction of an intermediate ketone. Luffarin I against human solid tumor cell lines showed antiproliferative activities (GI(50)) in the range 12–17 μM. |
format | Online Article Text |
id | pubmed-4413218 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-44132182015-05-07 Synthesis and Bioactivity of Luffarin I Urosa, Aitor Marcos, Isidro S. Díez, David Lithgow, Anna Plata, Gabriela B. Padrón, José M. Basabe, Pilar Mar Drugs Article The first synthesis of Luffarin I, sesterterpenolide isolated from sponge Luffariella geometrica, has been accomplished from commercially available sclareol. The key strategy involved in this synthesis is the diastereoselective reduction of an intermediate ketone. Luffarin I against human solid tumor cell lines showed antiproliferative activities (GI(50)) in the range 12–17 μM. MDPI 2015-04-20 /pmc/articles/PMC4413218/ /pubmed/25903281 http://dx.doi.org/10.3390/md13042407 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 | Article Urosa, Aitor Marcos, Isidro S. Díez, David Lithgow, Anna Plata, Gabriela B. Padrón, José M. Basabe, Pilar Synthesis and Bioactivity of Luffarin I |
title | Synthesis and Bioactivity of Luffarin I |
title_full | Synthesis and Bioactivity of Luffarin I |
title_fullStr | Synthesis and Bioactivity of Luffarin I |
title_full_unstemmed | Synthesis and Bioactivity of Luffarin I |
title_short | Synthesis and Bioactivity of Luffarin I |
title_sort | synthesis and bioactivity of luffarin i |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4413218/ https://www.ncbi.nlm.nih.gov/pubmed/25903281 http://dx.doi.org/10.3390/md13042407 |
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