Zhong-jing Huang, Rui-yun Yang, Xianhong Yin
Jan 1, 2010
Citations
1
Influential Citations
24
Citations
Quality indicators
Journal
Magnetic Resonance in Chemistry
Abstract
The structure elucidations and complete 1H and 13C NMR assignments are reported for two new xanthone derivatives: 1,7‐dihydroxy‐2‐methoxy‐3‐(3‐methylbut‐2‐enyl)‐9H‐xanthen‐9‐one (1) and 1‐hydroxy‐4,7‐dimethoxy‐6‐(3‐oxobutyl)‐9H‐xanthen‐9‐one (2). Both of these secondary metabolites were isolated from the fermentation medium of a mangrove endophytic fungus (No. ZH19). High‐resolution electron impact mass spectrometry (HREIMS), Fourier transform infrared (FT‐IR) absorption spectrometry, and NMR experiments including gCOSY, gHMQC, and gHMBC were used for the determination of the structures and NMR spectral assignments. Preliminary pharmacological test showed that compounds (1) and (2) inhibited KB cells with IC50 values of 20 and 35 µmol/ml, and KBV200 cells with IC50 values of 30 and 41 µmol/ml, respectively. Copyright © 2009 John Wiley & Sons, Ltd.