SphK2 confers 5-fluorouracil resistance to colorectal cancer via upregulating H3K56ac-mediated DPD expression von Zhang, Yu-Hang, Shi, Wen-Na, Wu, Shu-Hua, Miao, Rong-Rong, Sun, Shi-Yue, Luo, Dong-Dong, Wan, Sheng-Biao, Guo, Zhi-Kun, Wang, Wen-Yu, Yu, Xin-Feng, Cui, Shu-Xiang, Qu, Xian-Jun

Volltext

Increased S1P induces S1PR2 internalization to blunt the sensitivity of colorectal cancer to 5-fluorouracil via promoting intracellular uracil generation von Zhang, Yu-hang, Cui, Shu-xiang, Wan, Sheng-biao, Wu, Shu-hua, Qu, Xian-jun

Volltext

Synthesis of methylated quercetin derivatives and their reversal activities on P-gp- and BCRP-mediated multidrug resistance tumour cells von Yuan, Jian, Wong, Iris L.K., Jiang, Tao, Wang, Si Wen, Liu, Tao, Jin Wen, Bin, Chow, Larry M.C., Wan Sheng, Biao

Volltext

Structural modification of oridonin via DAST induced rearrangement von Luo, Dong-Dong, Peng, Kai, Yang, Jia-Yu, Piyachaturawat, Pawinee, Saengsawang, Witchuda, Ao, Lei, Zhao, Wan-Zhou, Tang, Yu, Wan, Sheng-Biao

Volltext

Organocatalytic asymmetric synthesis of both cis- and trans-configured pyrano[2,3-b]chromenes via different dehydration pathways von Xue-Jiao Lv, Wei-Wei, Zhao, Ying-Han, Chen, Sheng-Biao Wan, Yan-Kai, Liu

Volltext

S1PR2 inhibitors potently reverse 5-FU resistance by downregulating DPD expression in colorectal cancer von Zhang, Yu-Hang, Luo, Dong-Dong, Wan, Sheng-Biao, Qu, Xian-Jun

Volltext

Synthesis and evaluation of stereoisomers of methylated catechin and epigallocatechin derivatives on modulating P-glycoprotein-mediated multidrug resistance in cancers von Wong, Iris L.K., Wang, Xing-kai, Liu, Zhen, Sun, Wenqin, Li, Fu-xing, Wang, Bao-chao, Li, Peng, Wan, Sheng-biao, Chow, Larry M.C.

Volltext

Potent and Nontoxic Chemosensitizer of P‑Glycoprotein-Mediated Multidrug Resistance in Cancer: Synthesis and Evaluation of Methylated Epigallocatechin, Gallocatechin, and Dihydromy... von Wong, Iris L. K, Wang, Bao-Chao, Yuan, Jian, Duan, Liang-Xing, Liu, Zhen, Liu, Tao, Li, Xue-Min, Hu, Xuesen, Zhang, Xiao-Yu, Jiang, Tao, Wan, Sheng-Biao, Chow, Larry M. C

Volltext

Novel α-Lipoic Acid/3- n -Butylphthalide Conjugate Enhances Protective Effects against Oxidative Stress and 6-OHDA Induced Neuronal Damage von Uppakara, Kwanchanok, Jamornwan, Sopana, Duan, Liang-Xing, Yue, Kai-Rui, Sunrat, Chotchanit, Dent, Erik W, Wan, Sheng-Biao, Saengsawang, Witchuda

Volltext

First total synthesis of marine alkaloid hyrtiosulawesine von Zhang, Pu Yong, Wan, Sheng Biao, Ren, Su Mei, Jiang, Tao

Volltext

First preparation of a novel polyol resin for purifying arylboronic acids von Liu, Fu Long, Wan, Sheng Biao, Jiang, Tao

Volltext

Facile synthesis of a 4-anilinoquinazoline dimer by Suzuki cross-coupling reaction von Chen, Shao Peng, Sun, Yue, Wan, Sheng Biao, Jiang, Tao

Volltext

First total synthesis of eudistalbin A von Zhang, Pu Yong, Wang, Jun Lei, Wan, Sheng Biao, Jiang, Tao

Volltext

Methylation suppresses the proteasome-inhibitory function of green tea polyphenols von Landis-Piwowar, Kristin R., Wan, Sheng Biao, Wiegand, Richard A., Kuhn, Deborah J., Chan, Tak Hang, Dou, Q. Ping

Volltext

Modification of marine natural product ningalin B and SAR study lead to potent P-glycoprotein inhibitors von Yang, Chao, Wong, Iris L K, Jin, Wen Bin, Jiang, Tao, Chow, Larry M C, Wan, Sheng Biao

Volltext

Antitumor activity of novel fluoro-substituted (–)-epigallocatechin-3-gallate analogs von Yang, Huanjie, Sun, Dong Kui, Chen, Di, Cui, Qiuzhi Cindy, Gu, Yan Yan, Jiang, Tao, Chen, Wei, Wan, Sheng Biao, Dou, Q. Ping

Volltext

Study of the green tea polyphenols catechin-3-gallate (CG) and epicatechin-3-gallate (ECG) as proteasome inhibitors von Wan, Sheng Biao, Chen, Di, Ping Dou, Q., Hang Chan, Tak

Volltext

Regiospecific and enantioselective synthesis of methylated metabolites of tea catechins von Wan, Sheng Biao, Ping Dou, Q., Chan, Tak Hang

Volltext

Enantioselective synthesis of afzelechin and epiafzelechin von Wan, Sheng Biao, Chan, Tak Hang

Volltext

Structure–activity study of epi-gallocatechin gallate (EGCG) analogs as proteasome inhibitors von Wan, Sheng Biao, Landis-Piwowar, Kristin R., Kuhn, Deborah J., Chen, Di, Dou, Q. Ping, Chan, Tak Hang

Volltext