Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Hongrui Song"'
Publikováno v:
AIP Advances, Vol 14, Iss 1, Pp 015126-015126-11 (2024)
When locating multiple magnetic targets, the interference between each magnetic dipole is often ignored, we propose a method to detect and locate multiple weak magnetic target signals under the interference of strong magnetic sources. First, under di
Externí odkaz:
https://doaj.org/article/496263af3cfe4ed1a414d4a0c092fb45
Autor:
Shuo Wan, Yadong Sun, Jiamin Fu, Hongrui Song, Zhiqiang Xiao, Quanli Yang, Sanfeng Wang, Gongwang Yu, Peiran Feng, Wenkai Lv, Liang Luo, Zerong Guan, Feng Liu, Qinghua Zhou, Zhinan Yin, Meixiang Yang
Publikováno v:
Cell Death and Disease, Vol 13, Iss 10, Pp 1-14 (2022)
Abstract The mouse vaginal epithelium cyclically exhibits cell proliferation and differentiation in response to estrogen. Estrogen acts as an activator of mTOR signaling but its role in vaginal epithelial homeostasis is unknown. We analyzed reproduct
Externí odkaz:
https://doaj.org/article/4cac7673fd9949eb9a20103e2f44a646
Publikováno v:
AIP Advances, Vol 13, Iss 1, Pp 015033-015033-9 (2023)
The study of ocean wave energy harvesting technology is of great importance in the field of distributed sensor energy supply. Aiming at the problems of insufficient output power, single direction of collecting vibration, restricted working frequency
Externí odkaz:
https://doaj.org/article/12e1dbe84d57403b8e6b2299efaa7af6
Autor:
Junhai Xiao, Yigang Tong, Xiaohong Yang, Fan Feng, Yuhui Hua, Yingying Yu, Mingming Zhao, Hongrui Song
Publikováno v:
Molecules, Vol 18, Iss 3, Pp 3266-3278 (2013)
A novel series of N-sulfonyl homoserine lactone derivatives 5a–l has been designed, synthesized and evaluated for quorum sensing inhibitory activities towards violacein production. Of the compounds synthesized, compound 5h was found to possess an e
Externí odkaz:
https://doaj.org/article/5c3029abbfcb4e9f9f94e6e22dbda012
Autor:
Lijian Zhang, Kang Tian, Yongqiang Li, Lei Lei, Aifang Qin, Lijuan Zhang, Hongrui Song, Lianchao Huo, Lijing Zhang, Xiaofeng Jin, Zhufang Shen, Zhiqiang Feng
Publikováno v:
Acta Pharmaceutica Sinica B, Vol 2, Iss 6, Pp 588-597 (2012)
A series of novel phenyl-urea derivatives which can simultaneously activate glucokinase (GK) and peroxisome proliferator-activated receptor γ (PPARγ) was designed and prepared, and their activation of GK and PPARγ was evaluated. The structure–ac
Externí odkaz:
https://doaj.org/article/36462f9313d04715b0cc325b8d279b33
Autor:
Huaiwei Ding, Zhe Chen, Cunlong Zhang, Tian Xin, Yini Wang, Hongrui Song, Yuyang Jiang, Yuzong Chen, Yongnan Xu, Chunyan Tan
Publikováno v:
Molecules, Vol 17, Iss 4, Pp 4703-4716 (2012)
A series of novel compounds bearing imidazo[2,1-b]thiazole scaffolds were designed and synthesized based on the optimization of the virtual screening hit compound N-(6-morpholinopyridin-3-yl)-2-(6-phenylimidazo[2,1-b]thiazol-3-yl)acetamide (5a), and
Externí odkaz:
https://doaj.org/article/4983bfc8003c4f48a193910e18585d16
Autor:
Chunyan Tan, Yuzong Chen, Yongnan Xu, Yuyang Jiang, Hongrui Song, Yini Wang, Cunlong Zhang, Tian Xin, Zhe Chen, Huaiwei Ding
Publikováno v:
Molecules, Vol 17, Iss 4, Pp 4703-4716 (2012)
A series of novel compounds bearing imidazo[2,1-b]thiazole scaffolds were designed and synthesized based on the optimization of the virtual screening hit compound N-(6-morpholinopyridin-3-yl)-2-(6-phenylimidazo[2,1-b]thiazol-3-yl)acetamide (5a), and
Externí odkaz:
https://doaj.org/article/828f8cdbdce14c7db25ddabf1c06513a
Publikováno v:
Molecules, Vol 16, Iss 8, Pp 6684-6700 (2011)
Combretastatin A-4 (CA-4), its analogues and their excellent antitumoral and antivascular activities, have attracted considerable interest of medicinal chemists. In this article, a docking simulation was used to identify molecules having the same bin
Externí odkaz:
https://doaj.org/article/8a8a474d0d6944baad3f2155bacd6410
Autor:
Huaiwei Ding, Kai Chen, Bingke Song, Chenglong Deng, Wei Li, Li Niu, Mengxuan Bai, Hongrui Song, Lijuan Zhang
Publikováno v:
Molecules, Vol 23, Iss 1, p 85 (2017)
Two series of benzamides compounds bearing piperidine groups were synthesized and the Gli-luc luciferase activity was screened by Gys-luc luciferase gene detection method. Compound 5q showed promising inhibition of hedgehog (Hh) signaling pathway. To
Externí odkaz:
https://doaj.org/article/2ee7894d254f42f588fd3a757bd11e93
Autor:
Xianyu Yao, Xiuli Sun, Qi Feng, Yapeng Liu, Yuxuan Liu, Hongrui Song, Kairui Zhu, Shuangchun Yang
Publikováno v:
Chemistry and Technology of Fuels and Oils. 59:146-165
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c59aaa4e385ad60e104638a255d47c21
https://doi.org/10.1007/s10553-023-01513-9
https://doi.org/10.1007/s10553-023-01513-9