Tersone A-G, New Pyridone Alkaloids from the Deep-Sea Fungus Phomopsis tersa

Four phenylfuropyridone racemates, (±)-tersones A-C and E ( - , ), one phenylpyridone racemate, (±)-tersone D ( ), one new pyridine alkaloid, tersone F ( ), single new phenylfuropyridone, tersone G ( ) and two known analogs and were isolated from the deep-sea fungus . Their structures and absolute c...

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Veröffentlicht in:Marine drugs 2019-07, Vol.17 (7), p.394
Hauptverfasser: Chen, Shan-Chong, Liu, Zhao-Ming, Tan, Hai-Bo, Chen, Yu-Chan, Li, Sai-Ni, Li, Hao-Hua, Guo, Heng, Zhu, Shuang, Liu, Hong-Xin, Zhang, Wei-Min
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Sprache:eng
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Zusammenfassung:Four phenylfuropyridone racemates, (±)-tersones A-C and E ( - , ), one phenylpyridone racemate, (±)-tersone D ( ), one new pyridine alkaloid, tersone F ( ), single new phenylfuropyridone, tersone G ( ) and two known analogs and were isolated from the deep-sea fungus . Their structures and absolute configurations were characterized on the basis of comprehensive spectroscopic analyses, single-crystal X-ray diffraction experiments, and electronic circular dichroism (ECD) calculations. Moreover, compounds - were evaluated for in vitro antimicrobial and cytotoxic activity. Compounds and exhibited antibacterial activity against with the MIC value of 31.5 μg/mL, while compound showed cytoxic activities against SF-268, MCF-7, HepG-2 and A549 cell lines with IC values of 32.0, 29.5, 39.5 and 33.2 μM, respectively.
ISSN:1660-3397
1660-3397
DOI:10.3390/md17070394