Zobrazeno 1 - 10
of 57
pro vyhledávání: '"Han, Fangbin"'
Autor:
Liu, Nan, Wang, Shuai, Li, Munan, Zhao, Nan, Wang, Deyu, Zhang, Rui, Yu, Mingxin, Zhao, Luoyi, Zhang, Siwei, Han, Fangbin, Zhao, Ying, Liu, Quan
Publikováno v:
In Pharmacological Research October 2024 208
Publikováno v:
Applied Physics Letters,108, 102405 (2016)
We develop a method for universally resolving the important issue of separating the inverse spin Hall effect (ISHE) from spin rectification effect (SRE) signal. This method is based on the consideration that the two effects depend on the spin injecti
Externí odkaz:
http://arxiv.org/abs/1512.01870
Autor:
Han, Fangbin, Zhou, Ming-Ming
Publikováno v:
In Cell Chemical Biology 18 April 2019 26(4):468-470
Akademický článek
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Autor:
Ren, Chunyan, Zhang, Guangtao, Han, Fangbin, Fu, Shibo, Cao, Yingdi, Zhang, Fan, Zhang, Qiang, Meslamani, Jamel, Xu, Yaoyao, Ji, Donglei, Cao, Lingling, Zhou, Qian, Cheung, Ka-lung, Sharma, Rajal, Babault, Nicolas, Yi, Zhengzi, Zhang, Weijia, Walsh, Martin J., Zeng, Lei, Zhou, Ming-Ming
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 2018 Jul . 115(31), 7949-7954.
Externí odkaz:
https://www.jstor.org/stable/26529360
Autor:
Lin, Songwen, Wang, Chunyang, Ji, Ming, Wu, Deyu, Lv, Yuanhao, Sheng, Li, Han, Fangbin, Dong, Yi, Zhang, Kehui, Yang, Yakun, Li, Yan, Chen, Xiaoguang, Xu, Heng
Publikováno v:
In Bioorganic & Medicinal Chemistry 1 February 2018 26(3):637-646
Akademický článek
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Publikováno v:
In Journal of Pharmaceutical and Biomedical Analysis 2007 44(5):1127-1132
Autor:
Xichen Lin, John D. Elliott, Zhijun Xiang, Han Fangbin, Sijie Lu, Yaobang Cheng, Yan Xu, Stewart Leung, Feng Ren, Yong-Gang Zhao, Wei Cai, Ling Zhou, Qian Liu, Qinghua Meng, Jia-Ning Xiang, Guifeng Zhang, Wang Yonghui, Ziqiang Cheng, Ting Yang, Yafei Huang, Qianqian Wu
Publikováno v:
ACS Medicinal Chemistry Letters. 6:787-792
A novel series of biaryl amides was identified as RORγt inhibitors through core replacement of a starting hit 1. Structure-activity relationship exploration on the biaryl moiety led to discovery of potent RORγt inhibitors with good oral bioavailabi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a75f4b025d5582c9797c1cbebfdef3ca
https://doi.org/10.1021/acsmedchemlett.5b00122
https://doi.org/10.1021/acsmedchemlett.5b00122
Autor:
Yan Li, Li Sheng, Yuanhao Lv, Heng Xu, Ming Ji, Yi Dong, Xiaoguang Chen, Deyu Wu, Songwen Lin, Kehui Zhang, Han Fangbin, Yakun Yang, Chunyang Wang
Publikováno v:
Bioorganicmedicinal chemistry. 26(3)
A series of new thienopyrimidine derivatives has been discovered as potent PI3K inhibitors. The systematic SAR studies for these analogues are described. Among them, 8a and 9a exhibit nanomolar enzymatic potencies and sub-micromolar cellular anti-pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::006fbce39f3a9d1541ab2ccf68779f28
https://pubmed.ncbi.nlm.nih.gov/29305298
https://pubmed.ncbi.nlm.nih.gov/29305298