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Bioactive Bis(indole) Alkaloids from a Spongosorites sp. Sponge
Six new bis(indole) alkaloids (1–6) along with eight known ones of the topsentin class were isolated from a Spongosorites sp. sponge of Korea. Based on the results of combined spectroscopic analyses, the structures of spongosoritins A–D (1–4) were determined to possess a 2-methoxy-1-imidazole-5-one...
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/PMC7824209/ https://www.ncbi.nlm.nih.gov/pubmed/33374750 http://dx.doi.org/10.3390/md19010003 |
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author | Park, Jae Sung Cho, Eunji Hwang, Ji-Yeon Park, Sung Chul Chung, Beomkoo Kwon, Oh-Seok Sim, Chung J. Oh, Dong-Chan Oh, Ki-Bong Shin, Jongheon |
author_facet | Park, Jae Sung Cho, Eunji Hwang, Ji-Yeon Park, Sung Chul Chung, Beomkoo Kwon, Oh-Seok Sim, Chung J. Oh, Dong-Chan Oh, Ki-Bong Shin, Jongheon |
author_sort | Park, Jae Sung |
collection | PubMed |
description | Six new bis(indole) alkaloids (1–6) along with eight known ones of the topsentin class were isolated from a Spongosorites sp. sponge of Korea. Based on the results of combined spectroscopic analyses, the structures of spongosoritins A–D (1–4) were determined to possess a 2-methoxy-1-imidazole-5-one core connecting the indole moieties, and these were linked by a linear urea bridge for spongocarbamides A (5) and B (6). The absolute configurations of spongosoritins were assigned by electronic circular dichroism (ECD) computation. The new compounds exhibited moderate inhibition against transpeptidase sortase A and weak inhibition against human pathogenic bacteria and A549 and K562 cancer cell lines. |
format | Online Article Text |
id | pubmed-7824209 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-78242092021-01-24 Bioactive Bis(indole) Alkaloids from a Spongosorites sp. Sponge Park, Jae Sung Cho, Eunji Hwang, Ji-Yeon Park, Sung Chul Chung, Beomkoo Kwon, Oh-Seok Sim, Chung J. Oh, Dong-Chan Oh, Ki-Bong Shin, Jongheon Mar Drugs Article Six new bis(indole) alkaloids (1–6) along with eight known ones of the topsentin class were isolated from a Spongosorites sp. sponge of Korea. Based on the results of combined spectroscopic analyses, the structures of spongosoritins A–D (1–4) were determined to possess a 2-methoxy-1-imidazole-5-one core connecting the indole moieties, and these were linked by a linear urea bridge for spongocarbamides A (5) and B (6). The absolute configurations of spongosoritins were assigned by electronic circular dichroism (ECD) computation. The new compounds exhibited moderate inhibition against transpeptidase sortase A and weak inhibition against human pathogenic bacteria and A549 and K562 cancer cell lines. MDPI 2020-12-23 /pmc/articles/PMC7824209/ /pubmed/33374750 http://dx.doi.org/10.3390/md19010003 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 | Article Park, Jae Sung Cho, Eunji Hwang, Ji-Yeon Park, Sung Chul Chung, Beomkoo Kwon, Oh-Seok Sim, Chung J. Oh, Dong-Chan Oh, Ki-Bong Shin, Jongheon Bioactive Bis(indole) Alkaloids from a Spongosorites sp. Sponge |
title | Bioactive Bis(indole) Alkaloids from a Spongosorites sp. Sponge |
title_full | Bioactive Bis(indole) Alkaloids from a Spongosorites sp. Sponge |
title_fullStr | Bioactive Bis(indole) Alkaloids from a Spongosorites sp. Sponge |
title_full_unstemmed | Bioactive Bis(indole) Alkaloids from a Spongosorites sp. Sponge |
title_short | Bioactive Bis(indole) Alkaloids from a Spongosorites sp. Sponge |
title_sort | bioactive bis(indole) alkaloids from a spongosorites sp. sponge |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7824209/ https://www.ncbi.nlm.nih.gov/pubmed/33374750 http://dx.doi.org/10.3390/md19010003 |
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