Cyclofarnesane sesquiterpenoids from the fungus Sanghuangporus sp.

被引:9
|
作者
Rajachan, Oue-artorn [1 ,2 ]
Sangdee, Aphidech [3 ]
Kanokmedhakul, Kwanjai [4 ,5 ]
Tontapha, Sarawut [6 ]
Amornkitbamrung, Vittaya [6 ]
Kanokmedhakul, Somdej [4 ,5 ]
机构
[1] Mahasarakham Univ, Fac Sci, Dept Chem, Mahasarakharn 44150, Thailand
[2] Mahasarakham Univ, Fac Sci, Ctr Excellence Innovat Chem, Mahasarakharn 44150, Thailand
[3] Mahasarakham Univ, Dept Biol, Microbiol & Appl Microbiol Res Unit, Fac Sci, Mahasarakharn 44150, Thailand
[4] Khon Kaen Univ, Fac Sci, Dept Chem, Nat Prod Res Unit, Khon Kaen 40002, Thailand
[5] Khon Kaen Univ, Fac Sci, Ctr Excellence Innovat Chem, Khon Kaen 40002, Thailand
[6] Khon Kaen Univ, Fac Sci, Dept Phys, Integrated Nanotechnol Res Ctr, Khon Kaen 40002, Thailand
关键词
Sanghuangporus sp; Hymenochaetaceae; Cyclofarnesane sesquiterpenoids; Antibacterial; PHELLINUS-LINTEUS; ACID; METABOLITES;
D O I
10.1016/j.phytol.2020.03.007
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
An antibacterial activity-guided phytochemical investigation of the fungus Sanghuangporus sp. resulted in the isolation of two new cyclofarnesane sesquiterpenoids, (4 S ,6 S)-4-hydroxy-gamma-ionylideneacetic acid (1) and (4 R ,5 R ,6 S)-5,14-dihydro-4-hydroxy-gamma-ionylideneacetic acid (2), together with three known compounds, gamma-io-nylideneacetic acid (3), 1 S-(2 E)-5-[(1R)-2,2-dimethyl-6-methylidenecyclohexyl]-3-methylpent-2-enoic acid (4), and D-mannitol (5). Their structures were elucidated using extensive spectroscopic data (IR, 1D and 2D NMR) and mass spectrometry. The absolute configurations of compounds 1 and 2 were identified by NOESY and comparisons of their experimental and calculated electronic circular dichroism spectral data. Compounds 1 , 3 , and 4 were evaluated for antibacterial activity against five bacterial strains (Staphylococcus aureus MSSA 2933, S. aureus MRSA 20651, Bacillus cereus ATCC 11778, Escherichia coli 25922, and Shigella dysenteriae 15110).
引用
收藏
页码:17 / 20
页数:4
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