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Alkaloids from Tabernaemontana divaricata combined with fluconazole to overcome fluconazole resistance in Candida albicans 期刊论文
BIOORGANIC CHEMISTRY, 2021, 卷号: 107, 页码: 104515
作者:  Zhang,Yu;  Bai,Xue;  Yuwen,Huan-Sha;  Guo,Ling-Li;  Liu,Jian-Wen;  Hao,Xiao-Jiang
浏览  |  Adobe PDF(1576Kb)  |  收藏  |  浏览/下载:142/52  |  提交时间:2022/04/02
Tabernaemontana divaricate  Taberdines A-K  Reversal of fluconazole resistance  Candida albicans  
Diterpenes with potential treatment of vitiligo from the aerials parts of Euphorbia antiquorum L 期刊论文
FITOTERAPIA, 2020
作者:  Yuan, Wen-Juan;  Gao, Wen-Fen;  Zhao, Jiang-Yu;  Zhang, Yu;  Chen, Duo-Zhi;  Li, Shun-Lin;  Di, Ying-Tong;  Hao, Xiao-Jiang
浏览  |  Adobe PDF(522Kb)  |  收藏  |  浏览/下载:205/80  |  提交时间:2021/01/05
Antiproliferative Aspidosperma-Type Monoterpenoid Indole Alkaloids from Bousigonia mekongensis Inhibit Tubulin Polymerization 期刊论文
MOLECULES, 2019, 卷号: 24, 期号: 7, 页码: 10
作者:  Zhang, Yu;  Goto, Masuo;  Oda, Akifumi;  Hsu, Pei-Ling;  Guo, Ling-Li;  Fu, Yan-Hui;  Morris-Natschke, Susan L.;  Hamel, Ernest;  Lee, Kuo-Hsiung;  Hao, Xiao-Jiang
浏览  |  Adobe PDF(3129Kb)  |  收藏  |  浏览/下载:296/32  |  提交时间:2019/07/29
aspidosperma-type  monoterpenoid indole alkaloids  antiproliferative activity  tubulin inhibitor  Bousigonia mekongensis  
Design, synthesis and structure-activity relationship optimization of phenanthridine derivatives as new Wnt/beta-catenin signalling pathway agonists 期刊论文
BIOORGANIC CHEMISTRY, 2019, 卷号: 84, 页码: 285-294
作者:  Chen, Duo-zhi;  Yang, Bi-juan;  He, Xiao-li;  Fan, Shi-rui;  Cai, Jie-yun;  Jing, Chen-xu;  Zhang, Heng;  Zhang, Yu;  Li, Lin;  Hao, Xiao-jiang
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Wnt/beta-catenin signalling pathway agonist  Phenanthridine derivatives  Structural optimization  Structure-activity relationships (SARs)  
Five new alkaloids from Aconitum apetalum (Ranunculaceae) 期刊论文
PHYTOCHEMISTRY LETTERS, 2019, 卷号: 29, 页码: 6-11
作者:  Hu, Zhan-Xing;  Tang, Hong-Yu;  Yan, Xiao-Hui;  Zeng, Yan-Rong;  Aisa, Haji Aker;  Zhang, Yu;  Hao, Xiao-Jiang
浏览  |  Adobe PDF(1765Kb)  |  收藏  |  浏览/下载:359/42  |  提交时间:2019/03/18
Aconitum apetalum  Diterpenoid alkaloids  Aporphine alkaloids  Anti-TMV  Antimicrobial  
Acoapetaludines A-K, C-20 and C-19-diterpenoid alkaloids from the whole plants of Aconitum apetalum (Huth) B.Fedtsch 期刊论文
PHYTOCHEMISTRY, 2019, 卷号: 167, 页码: UNSP 112111
作者:  Hu,Zhan-Xing;  An,Qiao;  Tang,Hong-Yu;  Chen,Zheng-Hong;  Aisa,Haji Aker;  Zhang,Yu;  Hao,Xiao-Jiang
浏览  |  Adobe PDF(912Kb)  |  收藏  |  浏览/下载:128/31  |  提交时间:2020/04/02
Munronin O, a potential activator for plant resistance 期刊论文
PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY, 2018, 卷号: 146, 页码: 13-18
作者:  Yan, Ying;  Tang, Lei;  Hu, Jiaqi;  Wang, Jianta;  Adelakun, Tiwalade Adegoke;  Yang, Dongqiong;  Di, Yingtong;  Zhang, Yu;  Hao, Xiaojiang
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Limonoids  Munronia Henryi Harms  Tobacco Mosaic Virus  Antiviral Activity  Plant Resistance  
Two novel diterpenoid heterodimers, Bisebracteolasins A and B, from Euphorbia ebracteolata Hayata, and the cancer chemotherapeutic potential of Bisebracteolasin A 期刊论文
SCIENTIFIC REPORTS, 2017, 卷号: 7, 页码: 1
作者:  Yuan, Wen-Juan;  Ding, Xiao;  Wang, Zhe;  Yang, Bi-Juan;  Li, Xiao-Nian;  Zhang, Yu;  Chen, Duo-Zhi;  Li, Shun-Lin;  Chen, Quan;  Di, Ying-Tong;  Aisa, Haji Akber;  Hao, Xiao-Jiang
浏览  |  Adobe PDF(3375Kb)  |  收藏  |  浏览/下载:319/63  |  提交时间:2017/12/18
Synthesis, Neuro-protection and Anti-cancer Activities of Simple Isatin Mannich and Schiff Bases 期刊论文
LETTERS IN DRUG DESIGN & DISCOVERY, 2016, 卷号: 13, 期号: 5, 页码: 395-400
作者:  Chen, Gang;  Ning, Yang;  Zhao, Wei;  Zhang, Yanqiu;  Zhang, Yu;  Hao, Xiaojiang;  Wang, Ye;  Mu, Shuzhen
浏览  |  Adobe PDF(1361Kb)  |  收藏  |  浏览/下载:312/77  |  提交时间:2016/08/22
Isatin  Mannich Base  Schiff Base  Synthesis  Neuro-protection  Anti-tumor  
Theoretical study of regioselectivity in the synthesis of spiro [pyrrolidine-2,3'-oxindole] compounds by [3+2] cycloaddition 期刊论文
RESEARCH ON CHEMICAL INTERMEDIATES, 2015, 卷号: 41, 期号: 7, 页码: 4987-4996
作者:  Chen, Gang;  Yang, Jing;  Gao, Suo;  Zhang, Yu;  Hao, Xiaojiang
Adobe PDF(1404Kb)  |  收藏  |  浏览/下载:183/46  |  提交时间:2015/12/17
Regioselectivity  Theoretical  Spiro-oxindole  [3+2] Cycloaddition