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Cytotoxic Furan- and Pyrrole-Containing Scalarane Sesterterpenoids Isolated from the Sponge Scalarispongia sp.

Three furan-containing scalarane sesterterpenoids (1–3) and a novel pyrrole-containing analog (4) were isolated from the sponge Scalarispongia species. Compound 3, reported in the literature as a synthetic derivative of furoscalarol 2, was for the first time isolated from a natural source. During th...

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Autores principales: Lee, Yeon-Ju, Kim, Su Hyun, Choi, Hansol, Lee, Hyi-Seung, Lee, Jong Seok, Shin, Hee Jae, Lee, Jihoon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6429051/
https://www.ncbi.nlm.nih.gov/pubmed/30818810
http://dx.doi.org/10.3390/molecules24050840
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author Lee, Yeon-Ju
Kim, Su Hyun
Choi, Hansol
Lee, Hyi-Seung
Lee, Jong Seok
Shin, Hee Jae
Lee, Jihoon
author_facet Lee, Yeon-Ju
Kim, Su Hyun
Choi, Hansol
Lee, Hyi-Seung
Lee, Jong Seok
Shin, Hee Jae
Lee, Jihoon
author_sort Lee, Yeon-Ju
collection PubMed
description Three furan-containing scalarane sesterterpenoids (1–3) and a novel pyrrole-containing analog (4) were isolated from the sponge Scalarispongia species. Compound 3, reported in the literature as a synthetic derivative of furoscalarol 2, was for the first time isolated from a natural source. During the separation performed using a silica column in the presence of methanol, 16-methoxy derivatives (5, 6) were obtained from the unintended reaction of 2. The isolated natural products 3 and 4 and the artifact 5 showed moderate to high cytotoxicity against six human cancer cell lines, whereas compound 6, the C-16 epimer of 5, showed no cytotoxicity at a concentration of 60 μΜ.
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spelling pubmed-64290512019-04-15 Cytotoxic Furan- and Pyrrole-Containing Scalarane Sesterterpenoids Isolated from the Sponge Scalarispongia sp. Lee, Yeon-Ju Kim, Su Hyun Choi, Hansol Lee, Hyi-Seung Lee, Jong Seok Shin, Hee Jae Lee, Jihoon Molecules Communication Three furan-containing scalarane sesterterpenoids (1–3) and a novel pyrrole-containing analog (4) were isolated from the sponge Scalarispongia species. Compound 3, reported in the literature as a synthetic derivative of furoscalarol 2, was for the first time isolated from a natural source. During the separation performed using a silica column in the presence of methanol, 16-methoxy derivatives (5, 6) were obtained from the unintended reaction of 2. The isolated natural products 3 and 4 and the artifact 5 showed moderate to high cytotoxicity against six human cancer cell lines, whereas compound 6, the C-16 epimer of 5, showed no cytotoxicity at a concentration of 60 μΜ. MDPI 2019-02-27 /pmc/articles/PMC6429051/ /pubmed/30818810 http://dx.doi.org/10.3390/molecules24050840 Text en © 2019 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 (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Communication
Lee, Yeon-Ju
Kim, Su Hyun
Choi, Hansol
Lee, Hyi-Seung
Lee, Jong Seok
Shin, Hee Jae
Lee, Jihoon
Cytotoxic Furan- and Pyrrole-Containing Scalarane Sesterterpenoids Isolated from the Sponge Scalarispongia sp.
title Cytotoxic Furan- and Pyrrole-Containing Scalarane Sesterterpenoids Isolated from the Sponge Scalarispongia sp.
title_full Cytotoxic Furan- and Pyrrole-Containing Scalarane Sesterterpenoids Isolated from the Sponge Scalarispongia sp.
title_fullStr Cytotoxic Furan- and Pyrrole-Containing Scalarane Sesterterpenoids Isolated from the Sponge Scalarispongia sp.
title_full_unstemmed Cytotoxic Furan- and Pyrrole-Containing Scalarane Sesterterpenoids Isolated from the Sponge Scalarispongia sp.
title_short Cytotoxic Furan- and Pyrrole-Containing Scalarane Sesterterpenoids Isolated from the Sponge Scalarispongia sp.
title_sort cytotoxic furan- and pyrrole-containing scalarane sesterterpenoids isolated from the sponge scalarispongia sp.
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6429051/
https://www.ncbi.nlm.nih.gov/pubmed/30818810
http://dx.doi.org/10.3390/molecules24050840
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