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Neo-Aplysiatoxin A Isolated from Okinawan Cyanobacterium Moorea Producens
A new aplysiatoxin derivative, neo-aplysiatoxin A (1), along with seven known compounds, neo-debromoaplysiatoxin A (2), dolastatin 3 (3), lyngbic acid (4), malyngamide M (5), hermitamide A (6), (−)-loliolide (7), and (+)-epiloliolide (8), was isolated from the Okinawan cyanobacterium Moorea producen...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7037229/ https://www.ncbi.nlm.nih.gov/pubmed/31978978 http://dx.doi.org/10.3390/molecules25030457 |
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author | Kawaguchi, Mioko Satake, Masayuki Zhang, Bo-Tao Xiao, Yue-Yun Fukuoka, Masayuki Uchida, Hajime Nagai, Hiroshi |
author_facet | Kawaguchi, Mioko Satake, Masayuki Zhang, Bo-Tao Xiao, Yue-Yun Fukuoka, Masayuki Uchida, Hajime Nagai, Hiroshi |
author_sort | Kawaguchi, Mioko |
collection | PubMed |
description | A new aplysiatoxin derivative, neo-aplysiatoxin A (1), along with seven known compounds, neo-debromoaplysiatoxin A (2), dolastatin 3 (3), lyngbic acid (4), malyngamide M (5), hermitamide A (6), (−)-loliolide (7), and (+)-epiloliolide (8), was isolated from the Okinawan cyanobacterium Moorea producens. Their structures were elucidated on the basis of spectroscopic data, including high-resolution mass spectrometry and nuclear magnetic resonance. The compounds were evaluated for cytotoxic and diatom growth inhibition activities. |
format | Online Article Text |
id | pubmed-7037229 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-70372292020-03-11 Neo-Aplysiatoxin A Isolated from Okinawan Cyanobacterium Moorea Producens Kawaguchi, Mioko Satake, Masayuki Zhang, Bo-Tao Xiao, Yue-Yun Fukuoka, Masayuki Uchida, Hajime Nagai, Hiroshi Molecules Communication A new aplysiatoxin derivative, neo-aplysiatoxin A (1), along with seven known compounds, neo-debromoaplysiatoxin A (2), dolastatin 3 (3), lyngbic acid (4), malyngamide M (5), hermitamide A (6), (−)-loliolide (7), and (+)-epiloliolide (8), was isolated from the Okinawan cyanobacterium Moorea producens. Their structures were elucidated on the basis of spectroscopic data, including high-resolution mass spectrometry and nuclear magnetic resonance. The compounds were evaluated for cytotoxic and diatom growth inhibition activities. MDPI 2020-01-22 /pmc/articles/PMC7037229/ /pubmed/31978978 http://dx.doi.org/10.3390/molecules25030457 Text en © 2020 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 Kawaguchi, Mioko Satake, Masayuki Zhang, Bo-Tao Xiao, Yue-Yun Fukuoka, Masayuki Uchida, Hajime Nagai, Hiroshi Neo-Aplysiatoxin A Isolated from Okinawan Cyanobacterium Moorea Producens |
title | Neo-Aplysiatoxin A Isolated from Okinawan Cyanobacterium Moorea Producens |
title_full | Neo-Aplysiatoxin A Isolated from Okinawan Cyanobacterium Moorea Producens |
title_fullStr | Neo-Aplysiatoxin A Isolated from Okinawan Cyanobacterium Moorea Producens |
title_full_unstemmed | Neo-Aplysiatoxin A Isolated from Okinawan Cyanobacterium Moorea Producens |
title_short | Neo-Aplysiatoxin A Isolated from Okinawan Cyanobacterium Moorea Producens |
title_sort | neo-aplysiatoxin a isolated from okinawan cyanobacterium moorea producens |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7037229/ https://www.ncbi.nlm.nih.gov/pubmed/31978978 http://dx.doi.org/10.3390/molecules25030457 |
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