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Bromopyrrole Alkaloids from the Sponge Agelas kosrae
Two new sceptrin derivatives (1,2) and eight structurally-related known bromopyrrole-bearing alkaloids were isolated from the tropical sponge Agelas kosrae. By a combination of spectroscopic methods, the new compounds, designated dioxysceptrin (1) and ageleste C (2), were determined to be structural...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6316234/ https://www.ncbi.nlm.nih.gov/pubmed/30563015 http://dx.doi.org/10.3390/md16120513 |
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author | Kwon, Oh-Seok Kim, Donghwa Kim, Heegyu Lee, Yeon-Ju Lee, Hyi-Seung Sim, Chung J. Oh, Dong-Chan Lee, Sang Kook Oh, Ki-Bong Shin, Jongheon |
author_facet | Kwon, Oh-Seok Kim, Donghwa Kim, Heegyu Lee, Yeon-Ju Lee, Hyi-Seung Sim, Chung J. Oh, Dong-Chan Lee, Sang Kook Oh, Ki-Bong Shin, Jongheon |
author_sort | Kwon, Oh-Seok |
collection | PubMed |
description | Two new sceptrin derivatives (1,2) and eight structurally-related known bromopyrrole-bearing alkaloids were isolated from the tropical sponge Agelas kosrae. By a combination of spectroscopic methods, the new compounds, designated dioxysceptrin (1) and ageleste C (2), were determined to be structural analogs of each other that differ at the imidazole moiety. Dioxysceptrin was also found to exist as a mixture of α-amido epimers. The sceptrin alkaloids exhibited weak cytotoxicity against cancer cells. Compounds 1 and 2 also moderately exhibited anti-angiogenic and isocitrate lyase-inhibitory activities, respectively. |
format | Online Article Text |
id | pubmed-6316234 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-63162342019-01-10 Bromopyrrole Alkaloids from the Sponge Agelas kosrae Kwon, Oh-Seok Kim, Donghwa Kim, Heegyu Lee, Yeon-Ju Lee, Hyi-Seung Sim, Chung J. Oh, Dong-Chan Lee, Sang Kook Oh, Ki-Bong Shin, Jongheon Mar Drugs Article Two new sceptrin derivatives (1,2) and eight structurally-related known bromopyrrole-bearing alkaloids were isolated from the tropical sponge Agelas kosrae. By a combination of spectroscopic methods, the new compounds, designated dioxysceptrin (1) and ageleste C (2), were determined to be structural analogs of each other that differ at the imidazole moiety. Dioxysceptrin was also found to exist as a mixture of α-amido epimers. The sceptrin alkaloids exhibited weak cytotoxicity against cancer cells. Compounds 1 and 2 also moderately exhibited anti-angiogenic and isocitrate lyase-inhibitory activities, respectively. MDPI 2018-12-17 /pmc/articles/PMC6316234/ /pubmed/30563015 http://dx.doi.org/10.3390/md16120513 Text en © 2018 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 | Article Kwon, Oh-Seok Kim, Donghwa Kim, Heegyu Lee, Yeon-Ju Lee, Hyi-Seung Sim, Chung J. Oh, Dong-Chan Lee, Sang Kook Oh, Ki-Bong Shin, Jongheon Bromopyrrole Alkaloids from the Sponge Agelas kosrae |
title | Bromopyrrole Alkaloids from the Sponge Agelas kosrae |
title_full | Bromopyrrole Alkaloids from the Sponge Agelas kosrae |
title_fullStr | Bromopyrrole Alkaloids from the Sponge Agelas kosrae |
title_full_unstemmed | Bromopyrrole Alkaloids from the Sponge Agelas kosrae |
title_short | Bromopyrrole Alkaloids from the Sponge Agelas kosrae |
title_sort | bromopyrrole alkaloids from the sponge agelas kosrae |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6316234/ https://www.ncbi.nlm.nih.gov/pubmed/30563015 http://dx.doi.org/10.3390/md16120513 |
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