Citation: Hao Zhou, Ya-Bin Yang, Rong-Ting Duan, Xue-Qiong Yang, Ju-Cheng Zhang, Xiao-Guang Xie, Li-Xing Zhao, Zhong-Tao Ding. Neopeapyran, an unusual furo[2, 3b]pyran analogue and turnagainolide C from a soil Streptomyces sp. S2236[J]. Chinese Chemical Letters, ;2016, 27(7): 1044-1047. doi: 10.1016/j.cclet.2016.03.018 shu

Neopeapyran, an unusual furo[2, 3b]pyran analogue and turnagainolide C from a soil Streptomyces sp. S2236

a.
Key Laboratory of Medicinal Chemistry for Natural Resource, Ministry of Education, School of Chemical Science and Technology, Yunnan University, Kunming 650091, China
b.
Yunnan Institute of Microbiology, Yunnan University, Kunming 650091, China

Corresponding author: Zhong-Tao Ding, ztding@ynu.edu.cn
Received Date: 1 December 2015
Revised Date: 4 March 2016
Accepted Date: 7 March 2016
Available Online: 19 July 2016

Figures(3)

Neopeapyran (1), an unusual furo[2, 3b]pyran analogue, together with a new cyclopeptide, turnagainolide C (2), were isolated from Streptomyces sp. S2236 associated with the rhizosphere soil of Panax notoginseng. The planar structure and relative configuration of neopeapyran (1)) were elucidated on the basis of spectroscopic techniques, while the absolute configuration was determined by TDDFT calculation. The absolute configuration of turnagainolide C (2) was determined by partial hydrolysis, together with the advanced Marfey's method and spectroscopic analysis. The antimicrobial activities of these two compounds were also investigated.
- Streptomyces sp.,
- Furo[2, 3b]pyran analogue,
- Cyclopeptide,
- Structure elucidation,
- Antimicrobial activity
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1.
沈阳化工大学材料科学与工程学院沈阳 110142