张长生研究团队在《Journal of Natural Products》发表论文
副标题:
题目:α‑Pyrones with Diverse Hydroxy Substitutions from Three MarineDerived Nocardiopsis Strains |
作者:Haibo Zhang+, Kumar Saurav+, Ziquan Yu, Attila Mándi, Tibor Kurtán, Jie Li, Xinpeng Tian, Qingbo Zhang, Wenjun Zhang, Changsheng Zhang* |
刊物:Journal of Natural Products |
年卷期页:2016, 79(6): 1610-1618 |
摘要:Eight newα-pyrones1−8and three knownα-pyrones9−11were isolated from three marine-derivedNocardiopsisstrains SCSIO 10419, SCSIO 04583, and SCSIO KS107. The structures of compounds1−8were elucidated by comprehensive spectral analyses. The absolute configurations of 4-deoxyphomapyrone C (1), 4-deoxy-11-hydroxyphomapyrone C (3), 4-deoxy-7R-hydroxyphomapyrone C (5), and phomapyrone C (11) were determined by TDDFT-ECD calculations for the solution conformers, which revealed that the conformation of the side chain was decisive for the sign of the characteristic high-wavelength ECD transition. (−)-4-Deoxy-8-hydroxyphomapyrone C (4) was isolated from SCSIO 10419 and was deduced as a diastereomeric mixture containing (8S)- and (8R)-4-deoxy-8-hydroxyphomapyrone C in a ratio of 2.6:1 (8R:8S), by chiralphase HPLC analysis and Mosher’s ester analysis. Interestingly, 7-hydroxymucidone (9) was isolated from both SCSIO 04583 and SCSIO KS107, as an enantiomeric mixture containing (7S)-hydroxymucidone (major in9from SCSIO 04583) and (7R)-hydroxymucidone (major in9from SCSIO KS107).α-Pyrones3−5were identified as three isomers of phomapyrone C (11) with diverse hydroxy substitutions.α-Pyrones 10-hydroxymucidone (6), 4-hydroxymucidone (8), and9, differed in the position of the hydroxy group. Severalα-pyrones exhibited moderate growth inhibitory activity againstMicrococcus luteusandBacillus subtilis. |
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