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Amino Alcohols from the Ascidian Pseudodistoma sp
Seven new amino alcohol compounds, pseudoaminols A–G (1–7), were isolated from the ascidian Pseudodistoma sp. collected off the coast of Chuja-do, Korea. Structures of these new compounds were determined by analysis of the spectroscopic data and from chemical conversion. The presence of an N-carboxy...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4071600/ https://www.ncbi.nlm.nih.gov/pubmed/24962272 http://dx.doi.org/10.3390/md12063754 |
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author | Won, Tae Hyung You, Minjung Lee, So-Hyoung Rho, Boon Jo Oh, Dong-Chan Oh, Ki-Bong Shin, Jongheon |
author_facet | Won, Tae Hyung You, Minjung Lee, So-Hyoung Rho, Boon Jo Oh, Dong-Chan Oh, Ki-Bong Shin, Jongheon |
author_sort | Won, Tae Hyung |
collection | PubMed |
description | Seven new amino alcohol compounds, pseudoaminols A–G (1–7), were isolated from the ascidian Pseudodistoma sp. collected off the coast of Chuja-do, Korea. Structures of these new compounds were determined by analysis of the spectroscopic data and from chemical conversion. The presence of an N-carboxymethyl group in two of the new compounds (6 and 7) is unprecedented among amino alcohols. Several of these compounds exhibited moderate antimicrobial activity and cytotoxicity, as well as weak inhibitory activity toward Na(+)/K(+)-ATPase. |
format | Online Article Text |
id | pubmed-4071600 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-40716002014-06-26 Amino Alcohols from the Ascidian Pseudodistoma sp Won, Tae Hyung You, Minjung Lee, So-Hyoung Rho, Boon Jo Oh, Dong-Chan Oh, Ki-Bong Shin, Jongheon Mar Drugs Article Seven new amino alcohol compounds, pseudoaminols A–G (1–7), were isolated from the ascidian Pseudodistoma sp. collected off the coast of Chuja-do, Korea. Structures of these new compounds were determined by analysis of the spectroscopic data and from chemical conversion. The presence of an N-carboxymethyl group in two of the new compounds (6 and 7) is unprecedented among amino alcohols. Several of these compounds exhibited moderate antimicrobial activity and cytotoxicity, as well as weak inhibitory activity toward Na(+)/K(+)-ATPase. MDPI 2014-06-24 /pmc/articles/PMC4071600/ /pubmed/24962272 http://dx.doi.org/10.3390/md12063754 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 | Article Won, Tae Hyung You, Minjung Lee, So-Hyoung Rho, Boon Jo Oh, Dong-Chan Oh, Ki-Bong Shin, Jongheon Amino Alcohols from the Ascidian Pseudodistoma sp |
title | Amino Alcohols from the Ascidian Pseudodistoma sp |
title_full | Amino Alcohols from the Ascidian Pseudodistoma sp |
title_fullStr | Amino Alcohols from the Ascidian Pseudodistoma sp |
title_full_unstemmed | Amino Alcohols from the Ascidian Pseudodistoma sp |
title_short | Amino Alcohols from the Ascidian Pseudodistoma sp |
title_sort | amino alcohols from the ascidian pseudodistoma sp |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4071600/ https://www.ncbi.nlm.nih.gov/pubmed/24962272 http://dx.doi.org/10.3390/md12063754 |
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