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Monoindole Alkaloids from a Marine Sponge Spongosorites sp.
Seven (1–7) monoindole derivatives were isolated from the MeOH extract of a marine sponge Spongosorites sp. by bioactivity-guided fractionation. The planar structures were established on the basis of NMR and MS spectroscopic analyses. Compounds 1–5 are unique indole pyruvic acid derivatives. Compoun...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Molecular Diversity Preservation International
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2365689/ https://www.ncbi.nlm.nih.gov/pubmed/18463722 |
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author | Bao, Baoquan Zhang, Ping Lee, Yoonmi Hong, Jongki Lee, Chong-O. Jung, Jee H. |
author_facet | Bao, Baoquan Zhang, Ping Lee, Yoonmi Hong, Jongki Lee, Chong-O. Jung, Jee H. |
author_sort | Bao, Baoquan |
collection | PubMed |
description | Seven (1–7) monoindole derivatives were isolated from the MeOH extract of a marine sponge Spongosorites sp. by bioactivity-guided fractionation. The planar structures were established on the basis of NMR and MS spectroscopic analyses. Compounds 1–5 are unique indole pyruvic acid derivatives. Compounds 1–2 and 4–6 are isolated for the first time from a natural source although they were previously reported as synthetic intermediates. Compound 3 was defined as a new compound. Co-occurring bisindoles such as hamacanthins and topsentins might be biosynthesized by condensation of two units of these compounds. The compounds were tested for cytotoxicity against a panel of five human solid tumor cell lines, and compound 7 displayed weak activity. |
format | Text |
id | pubmed-2365689 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | Molecular Diversity Preservation International |
record_format | MEDLINE/PubMed |
spelling | pubmed-23656892008-05-07 Monoindole Alkaloids from a Marine Sponge Spongosorites sp. Bao, Baoquan Zhang, Ping Lee, Yoonmi Hong, Jongki Lee, Chong-O. Jung, Jee H. Mar Drugs Full Original Paper Seven (1–7) monoindole derivatives were isolated from the MeOH extract of a marine sponge Spongosorites sp. by bioactivity-guided fractionation. The planar structures were established on the basis of NMR and MS spectroscopic analyses. Compounds 1–5 are unique indole pyruvic acid derivatives. Compounds 1–2 and 4–6 are isolated for the first time from a natural source although they were previously reported as synthetic intermediates. Compound 3 was defined as a new compound. Co-occurring bisindoles such as hamacanthins and topsentins might be biosynthesized by condensation of two units of these compounds. The compounds were tested for cytotoxicity against a panel of five human solid tumor cell lines, and compound 7 displayed weak activity. Molecular Diversity Preservation International 2007-06-25 /pmc/articles/PMC2365689/ /pubmed/18463722 Text en © 2007 by MDPI |
spellingShingle | Full Original Paper Bao, Baoquan Zhang, Ping Lee, Yoonmi Hong, Jongki Lee, Chong-O. Jung, Jee H. Monoindole Alkaloids from a Marine Sponge Spongosorites sp. |
title | Monoindole Alkaloids from a Marine Sponge Spongosorites sp. |
title_full | Monoindole Alkaloids from a Marine Sponge Spongosorites sp. |
title_fullStr | Monoindole Alkaloids from a Marine Sponge Spongosorites sp. |
title_full_unstemmed | Monoindole Alkaloids from a Marine Sponge Spongosorites sp. |
title_short | Monoindole Alkaloids from a Marine Sponge Spongosorites sp. |
title_sort | monoindole alkaloids from a marine sponge spongosorites sp. |
topic | Full Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2365689/ https://www.ncbi.nlm.nih.gov/pubmed/18463722 |
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