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ABT-263 enhances sorafenib-induced apoptosis associated with Akt activity and the expression of Bax and p21 (CIP1/WAF1) in human cancer cells1 期刊论文
出版物, 3111, 期号: 0, 页码: 1-35
Authors:  Jingru Li;  Yicheng Chen;  Jiali Wan;  Xin Liu;  Chunrong Yu;  Wenhua Li
Adobe PDF(1198Kb)  |  Favorite  |  View/Download：214/1  |  Submit date：2017/07/24
Abt-263  Sorafenib  Combination Therapy  Cancer  
YC-1 inhibits proliferation of breast cancer cells by downregulating EZH2 expression via activation of c-Cbl and ERK 期刊论文
出版物, 3111, 期号: 0, 页码: 1-46
Authors:  Ling-Chu Chang;  Hui-Yi Lin;  Meng-Tung Tsai;  Ruey-Hwang Chou;  Fang-Yu Lee;  Che-Ming Teng;  Min-Tsang Hsieh;  Hsin-Yi Hung;  Li-Jiau Huang;  Yung-Luen Yu;  Sheng-Chu Kuo
Adobe PDF(1357Kb)  |  Favorite  |  View/Download：346/1  |  Submit date：2017/07/24
Yc-1  Triple-negative Breast Cancer  Erk  Ezh2  C-cbl  
三尖杉属植物生物碱成分研究和活性酯碱资源评价 学位论文
: 中国科学院大学, 2022
Authors:  余光兴
Adobe PDF(2195Kb)  |  Favorite  |  View/Download：46/0  |  Submit date：2024/05/14
三尖杉属,种子,三尖杉生物碱,分离鉴定,酯碱资源评价  Cephalotaxus,Seeds,Cephalotaxine alkaloids,Isolation and identification,Ester alkaloids resources evaluation  
皱叶酸模根的化学成分及生物活性研究 学位论文
: 中国科学院大学, 2022
Authors:  李永祥
Adobe PDF(4646Kb)  |  Favorite  |  View/Download：28/0  |  Submit date：2024/05/14
皱叶酸模，化学成分，生物活性，网络药理学  Rumex crispus L., Chemical composition, Biological activity, Network pharmacology  
愈创木烷倍半萜 ludartin 衍生物合成与抗 肝癌活性研究 学位论文
: 中国科学院大学, 2022
Authors:  孙金金
Adobe PDF(7657Kb)  |  Favorite  |  View/Download：8/0  |  Submit date：2024/05/14
Ludartin 衍生物合成  Synthesis of ludartin derivatives, Antihepatoma activity, HepG2 cells, Huh7 cells  抗肝癌活性  HepG2 细胞  Huh7 细胞  
海菜花化学成分研究和Telekin的结构改造 学位论文
: 中国科学院大学, 2022
Authors:  曾政权
Adobe PDF(4997Kb)  |  Favorite  |  View/Download：26/0  |  Submit date：2024/05/14
天然产物、海菜花、天名精、倍半萜内酯、结构修饰  Natural Products, Ottelia acuminata, Carpesium abrotanoides L., Sesquiterpene lactone, Structural modification  
Total synthesis of Lentinus giganteus glycans with antitumor activities via stereoselective alpha-glycosylation and orthogonal one-pot glycosylation strategies 期刊论文
CHEMICAL SCIENCE, 2022, 卷号: 13, 期号: 26, 页码: 7755-7764
Authors:  Zhang, Yunqin;  Hu, Yanlei;  Liu, Shanshan;  He, Haiqing;  Sun, Roujing;  Lu, Gang;  Xiao, Guozhi
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1,2-CIS O-GLYCOSYLATION  SELECTIVE SYNTHESIS  CHEMICAL-SYNTHESIS  OLIGOSACCHARIDE  GALACTOSYLATION  POLYSACCHARIDE  ALKYNYLBENZOATES  CONJUGATION  ANTIBODIES  CATALYSIS  
Design and synthesis of ludartin derivatives as potential anticancer agents against hepatocellular carcinoma 期刊论文
MEDICINAL CHEMISTRY RESEARCH, 2022, 卷号: 31, 期号: 7, 页码: 1224-1239
Authors:  Sun, Jin-Jin;  Wang, Jin-Ping;  Li, Tian-Ze;  Ma, Yun-Bao;  Xue, Dong;  Chen, Ji-Jun
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Ludartin derivatives  Antihepatoma activity  HepG2 cells  Huh7 cells  SESQUITERPENE LACTONES  CHEMICAL-CONSTITUENTS  GUAIANOLIDES  ANTITUMOR  ANALOGS  
Kadsura longipedunculata Finet & Gagnepain (Schisandraceae): An Overview of Botany, Traditional Uses, Phytochemistry and Pharmacological Activities 期刊论文
FORESTS, 2022, 卷号: 13, 期号: 8, 页码: 1281
Authors:  Idrees, Muhammad;  Zhang, Zhiyong;  Yaseen, Aftab;  Jiao, Yongqing;  Zheng, Xu
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Kadsura longipedunculata  phytochemistry  pharmacology  medicinal plant  LOWERS SERUM-CHOLESTEROL  ESSENTIAL OILS  DIBENZOCYCLOOCTADIENE LIGNANS  TRITERPENE DILACTONES  CHEMICAL-CONSTITUENTS  STRUCTURE ELUCIDATION  GENUS KADSURA  HETEROCLITA  STEMS  5-ALPHA-CHOLEST-8(14)-EN-3-BETA-OL-15-ONE  
Evaluation of the in vitro antioxidant and antitumor activity of extracts from Camellia fascicularis leaves 期刊论文
FRONTIERS IN CHEMISTRY, 2022, 卷号: 10, 页码: 1034785
Authors:  Peng, Xiaowei;  He, Xuhua;  Tang, Junrong;  Xiang, Jianying;  Deng, Jia;  Kan, Huan;  Zhang, Yingjun;  Zhang, Guiliang;  Zhao, Ping;  Liu, Yun
View  |  Adobe PDF(2352Kb)  |  Favorite  |  View/Download：8/5  |  Submit date：2024/08/21
Camellia fascicularis  extracts  active substances  antioxidant  antitumor  CELASTRUS-ORBICULATUS EXTRACT  ANTIOXIDANT ACTIVITIES  STRUCTURAL CHARACTERISTICS  ASSISTED EXTRACTION  VITRO ANTIOXIDANT  AQUEOUS EXTRACT  POLYSACCHARIDES  POLYPHENOLS  METASTASIS  APOPTOSIS