KIB OpenIR

Browse/Search Results:  1-10 of 11 Help

Selected(0)Clear Items/Page:    Sort:
Cytochalasans from the Endophytic Fungus Xylaria cf. curta with Resistance Reversal Activity against Fluconazole-Resistant Candida albicans 期刊论文
ORGANIC LETTERS, 2019, 卷号: 21, 期号: 4, 页码: 1108-1111
Authors:  Wang, Wen-Xuan;  Lei, Xinxiang;  Ai, Hong-Lian;  Bai, Xue;  Li, Jing;  He, Juan;  Li, Zheng-Hui;  Zheng, Yong-Sheng;  Feng, Tao;  Liu, Ji-Kai
Favorite  |  View/Download:33/0  |  Submit date:2019/03/25
Patterns and Controls of Light Use Efficiency in Four Contrasting Forest Ecosystems in Yunnan, Southwest China 期刊论文
JOURNAL OF GEOPHYSICAL RESEARCH-BIOGEOSCIENCES, 2019, 卷号: 124, 期号: 2, 页码: 293-311
Authors:  Fei, Xue-Hai;  Song, Qing-Hai;  Zhang, Yi-Ping;  Yu, Gui-Rui;  Zhang, Lei-Ming;  Sha, Li-Qing;  Liu, Yun-Tong;  Xu, Kun;  Chen, Hui;  Wu, Chuan-Sheng;  Chen, Ai-Guo;  Zhang, Shu-Bin;  Liu, Wei-Wei;  Huang, Hua;  Deng, Yun;  Qin, Hai-Lang;  Li, Pei-Guang;  Grace, John
Favorite  |  View/Download:22/0  |  Submit date:2019/04/15
ecosystem light use efficiency  critical factors  path analysis  climate change  forest ecosystems  eddy covariance  
Hydrocarbons mediate seed dispersal: a new mechanism of vespicochory 期刊论文
NEW PHYTOLOGIST, 2018, 卷号: 220, 期号: 3, 页码: 714-725
Authors:  Chen, Gao;  Wang, Zheng-Wei;  Wen, Ping;  Wei, Wei;  Chen, Ya;  Ai, Hui;  Sun, Wei-Bang
View  |  Adobe PDF(1782Kb)  |  Favorite  |  View/Download:232/0  |  Submit date:2018/11/12
Elaiosome  Myrmecochory  Seed Dispersal  Stemona  Vespa  Vespicochory  
Enantiomeric Pairs of Meroterpenoids with Diverse Heterocyclic Systems from Rhododendron nyingchiense 期刊论文
JOURNAL OF NATURAL PRODUCTS, 2018, 卷号: 81, 期号: 8, 页码: 1810-1818
Authors:  Huang, Guang-Hui;  Hu, Zhu;  Lei, Chun;  Wang, Pei-Pei;  Yang, Jing;  Li, Jing-Ya;  Li, Jia;  Hou, Ai-Jun
Favorite  |  View/Download:105/0  |  Submit date:2018/09/27
Nicotabin A, a Sesquiterpenoid Derivative from Nicotiana tabacum 期刊论文
ORGANIC LETTERS, 2017, 卷号: 19, 期号: 19, 页码: 5201-5203
Authors:  Feng, Tao;  Li, Xue-Mei;  He, Jun;  Ai, Hong-Lian;  Chen, He-Ping;  Li, Xiao-Nian;  Li, Zheng-Hui;  Liu, Ji-Kai
View  |  Adobe PDF(527Kb)  |  Favorite  |  View/Download:69/6  |  Submit date:2017/12/11
Cytotoxic steroidal saponins from Trillium kamtschaticum 期刊论文
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2017, 卷号: 27, 页码: 2267-2273
Authors:  Qin, Xu-Jie;  Si, Yong-Ai;  Chen, Yu;  Liu, Hui;  Ni, Wei;  Yan, Huan;  Shu, Tong;  Ji, Yun-Heng;  Liu, Hai-Yang
View  |  Adobe PDF(529Kb)  |  Favorite  |  View/Download:92/18  |  Submit date:2017/07/18
Trillium Kamtschaticum  Liliaceae  Steroidal Saponins  Cytotoxicity  
黄草乌种子萌发特性研究 期刊论文
种子, 2015, 期号: 12, 页码: 80-82
Authors:  艾洪莲;  何华杰;  杨曼思;  沙本才;  杨生超;  字淑慧
View  |  Adobe PDF(373Kb)  |  Favorite  |  View/Download:569/113  |  Submit date:2016/06/27
黄草乌  种子萌发  发芽率  发芽指数  
Four new C-18-diterpenoid alkaloids with analgesic activity from Aconitum weixiense 期刊论文
FITOTERAPIA, 2013, 卷号: 91, 页码: 280-283
Authors:  Zhao, Da-Ke;  Ai, Hong-Lian;  Zi, Shu-Hui;  Zhang, Li-Mei;  Yang, Sheng-Chao;  Guo, Hua-Chun;  Shen, Yong;  Chen, Yan-Ping;  Chen, Ji-Jun
Adobe PDF(323Kb)  |  Favorite  |  View/Download:343/56  |  Submit date:2014/01/13
Diterpenoid Alkaloids  Weisaconitines A-d  Analgesic Activity  Aconitum Weixiense  Ranunculaceae  
Three New C19-Diterpenoid Alkaloids from Aconitum transsectum 期刊论文
HELVETICA CHIMICA ACTA, 2012, 卷号: 95, 期号: 3, 页码: 509-513
Authors:  Shen, Yong;  Ai, Hong-Lian;  Cao, Tuan-Wu;  Wang, Jian-Jun;  Zi, Shu-Hui;  Zhang, Xue-Mei;  Chen, Ji-Jun
Adobe PDF(174Kb)  |  Favorite  |  View/Download:249/72  |  Submit date:2012/06/07
Aconitum Transsectum  AA?-?conitramines a?-?A?-?c  Alkaloids  
Two new compounds from an endophytic fungus Alternaria solani 期刊论文
JOURNAL OF ASIAN NATURAL PRODUCTS RESEARCH, 2012, 卷号: 14, 期号: 12, 页码: 1144-1148
Authors:  Ai, Hong-Lian;  Zhang, Li-Mei;  Chen, Yan-Ping;  Zi, Shu-Hui;  Xiang, Hong;  Zhao, Da-Ke;  Shen, Yong
View  |  Adobe PDF(82Kb)  |  Favorite  |  View/Download:82/16  |  Submit date:2015/06/17
Alternaria Solani  Aconitum Transsectum  7-dehydroxyl-zinniol  Anti-hbv Activity  20-hydroxyl-ergosta-4  6  8(14)  22-tetraen-3-one