Cargando…
The Isolation of a New S-Methyl Benzothioate Compound from a Marine-Derived Streptomyces sp.
The application of an HPLC bioactivity profiling/microtiter plate technique in conjunction with microprobe NMR instrumentation and access to the AntiMarin database has led to the isolation of a new 1. In this example, 1 was isolated from a cytotoxic fraction of an extract obtained from marine-derive...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3265089/ https://www.ncbi.nlm.nih.gov/pubmed/22291452 http://dx.doi.org/10.1155/2012/894708 |
_version_ | 1782222037125693440 |
---|---|
author | Mahyudin, Nor Ainy Blunt, John W. Cole, Anthony L. J. Munro, Murray H. G. |
author_facet | Mahyudin, Nor Ainy Blunt, John W. Cole, Anthony L. J. Munro, Murray H. G. |
author_sort | Mahyudin, Nor Ainy |
collection | PubMed |
description | The application of an HPLC bioactivity profiling/microtiter plate technique in conjunction with microprobe NMR instrumentation and access to the AntiMarin database has led to the isolation of a new 1. In this example, 1 was isolated from a cytotoxic fraction of an extract obtained from marine-derived Streptomyces sp. cultured on Starch Casein Agar (SCA) medium. The 1D and 2D (1)H NMR and ESIMS data obtained from 20 μg of compound 1 fully defined the structure. The known 2 was also isolated and readily dereplicated using this approach. |
format | Online Article Text |
id | pubmed-3265089 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-32650892012-01-30 The Isolation of a New S-Methyl Benzothioate Compound from a Marine-Derived Streptomyces sp. Mahyudin, Nor Ainy Blunt, John W. Cole, Anthony L. J. Munro, Murray H. G. J Biomed Biotechnol Research Article The application of an HPLC bioactivity profiling/microtiter plate technique in conjunction with microprobe NMR instrumentation and access to the AntiMarin database has led to the isolation of a new 1. In this example, 1 was isolated from a cytotoxic fraction of an extract obtained from marine-derived Streptomyces sp. cultured on Starch Casein Agar (SCA) medium. The 1D and 2D (1)H NMR and ESIMS data obtained from 20 μg of compound 1 fully defined the structure. The known 2 was also isolated and readily dereplicated using this approach. Hindawi Publishing Corporation 2012 2012-01-16 /pmc/articles/PMC3265089/ /pubmed/22291452 http://dx.doi.org/10.1155/2012/894708 Text en Copyright © 2012 Nor Ainy Mahyudin et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Mahyudin, Nor Ainy Blunt, John W. Cole, Anthony L. J. Munro, Murray H. G. The Isolation of a New S-Methyl Benzothioate Compound from a Marine-Derived Streptomyces sp. |
title | The Isolation of a New S-Methyl Benzothioate Compound from a Marine-Derived Streptomyces sp. |
title_full | The Isolation of a New S-Methyl Benzothioate Compound from a Marine-Derived Streptomyces sp. |
title_fullStr | The Isolation of a New S-Methyl Benzothioate Compound from a Marine-Derived Streptomyces sp. |
title_full_unstemmed | The Isolation of a New S-Methyl Benzothioate Compound from a Marine-Derived Streptomyces sp. |
title_short | The Isolation of a New S-Methyl Benzothioate Compound from a Marine-Derived Streptomyces sp. |
title_sort | isolation of a new s-methyl benzothioate compound from a marine-derived streptomyces sp. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3265089/ https://www.ncbi.nlm.nih.gov/pubmed/22291452 http://dx.doi.org/10.1155/2012/894708 |
work_keys_str_mv | AT mahyudinnorainy theisolationofanewsmethylbenzothioatecompoundfromamarinederivedstreptomycessp AT bluntjohnw theisolationofanewsmethylbenzothioatecompoundfromamarinederivedstreptomycessp AT coleanthonylj theisolationofanewsmethylbenzothioatecompoundfromamarinederivedstreptomycessp AT munromurrayhg theisolationofanewsmethylbenzothioatecompoundfromamarinederivedstreptomycessp AT mahyudinnorainy isolationofanewsmethylbenzothioatecompoundfromamarinederivedstreptomycessp AT bluntjohnw isolationofanewsmethylbenzothioatecompoundfromamarinederivedstreptomycessp AT coleanthonylj isolationofanewsmethylbenzothioatecompoundfromamarinederivedstreptomycessp AT munromurrayhg isolationofanewsmethylbenzothioatecompoundfromamarinederivedstreptomycessp |