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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
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.
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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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