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1 H and 13 C NMR assignments of three nitrogen containing compounds from the mangrove endophytic fungus (ZZF08)
Author(s) -
Tao Yiwen,
Zeng Xianjian,
Mou Chengbo,
Li Jun,
Cai Xiaoling,
She Zhigang,
Zhou Shining,
Lin Yongcheng
Publication year - 2008
Publication title -
magnetic resonance in chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.483
H-Index - 72
eISSN - 1097-458X
pISSN - 0749-1581
DOI - 10.1002/mrc.2194
Subject(s) - chemistry , mangrove , nitrogen , carbon 13 nmr , nuclear magnetic resonance spectroscopy , stereochemistry , organic chemistry , ecology , biology
A new natural product, named phomopsin A, 1‐(meta‐hydroxyphenyl)‐4‐hydroxy‐3‐isoquinolone (1), together with two known compounds cytochalasin H (2) and glucosylceramide (3), was isolated from the mangrove endophytic fungus Phomopsis sp. (ZZF08) obtained from the South China Sea coast. The structures were elucidated by 1D and 2D NMR experiments including COSY, HMQC, and HMBC. According to NMR and single‐crystal X‐ray diffraction, it was found that some assignments about 1 H and 13 C NMR data for cytochalasin H (2) were probably uncorrected in the previous reports. In our cytotoxicity assays, compound 1 showed moderate cytotoxicity toward KB cells with IC 50 at 28.0 µg ml −1 and KBv200 cells with IC 50 at 16.8 µg ml −1 , and compound 2 exhibited strong cytotoxicity toward KB cells and KBv200 cells with IC 50 less than 1.25 µg ml −1 . Copyright © 2008 John Wiley & Sons, Ltd.