Journal
PHYTOCHEMISTRY
Volume 66, Issue 9, Pages 1077-1082Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.phytochem.2005.03.014
Keywords
Scyphocephalium ochocoa; myristicaceae; high-throughput natural product chemistry; CapNMR (TM) probe; miniaturization; structure elucidation; cyclolignans; ocholignans; antibacterial
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Two 2,7 '-cyclolignans, ocholignans A and B, were obtained as mass-limited samples from Scyphocephalium ochocoa via high-throughput natural products chemistry methods. The rapid structure elucidation of each compound was primarily facilitated by NMR data acquisition using a capillary-scale NMR probe, CapNMR (TM) probe. Ocholignan A was found to possess significant in vitro antibacterial activity against Gram-positive bacteria methicillin-resistant Staphylococcus aureus ATCC 33591 and S. aureus 78-13607A with a MIC of 16 mu g/mL, respectively. (c) 2005 Elsevier Ltd. All rights reserved.
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