High-performance liquid chromatography, nuclear magnetic resonance (NMR) spectroscopy and sequential mass spectrometry (MS n ) have been combined to allow rapid and effective identification of metabolites in urine following administration of the novel non-nucleoside reverse transcriptase inhibitor,
Identification of two isomeric meroterpenoid naphthoquinones from Cordia linnaei by liquid chromatography–mass spectrometry and liquid chromatography–nuclear magnetic resonance spectroscopy
✍ Scribed by Jean-Robert Ioset; Jean-Luc Wolfender; Andrew Marston; Mahabir P. Gupta; Professor Kurt Hostettmann
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 98 KB
- Volume
- 10
- Category
- Article
- ISSN
- 0958-0344
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✦ Synopsis
The structures of two meroterpenoid naphthoquinones have been elucidated in a fraction of the dichloromethane extract from Cordia linnaei Stearn (Boraginaceae). These naphthoquinones were shown to be closely related structural isomers not separable by preparative chromatographic methods. High performance liquid chromatography coupled with mass spectrometry and nuclear magnetic resonance (NMR) spectroscopy was used for their structure determination within the mixture. Assignment of proton and carbon signals was achieved by a combination of on-flow liquid chromatography-proton NMR, and NMR experiments on the crude fraction.
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