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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...

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Detalles Bibliográficos
Autores principales: Bao, Baoquan, Zhang, Ping, Lee, Yoonmi, Hong, Jongki, Lee, Chong-O., Jung, Jee H.
Formato: Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International 2007
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.
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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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