41855-67-8Relevant academic research and scientific papers
Design and optimization of novel hydroxamate-based histone deacetylase inhibitors of bis-substituted aromatic amides bearing potent activities against tumor growth and metastasis
Yang, Feifei,Zhang, Tao,Wu, Haigang,Yang, Yang,Liu, Ning,Chen, Ang,Li, Qiang,Li, Jingjie,Qin, Liwen,Jiang, Beier,Wang, Xin,Pang, Xiufeng,Yi, Zhengfang,Liu, Mingyao,Chen, Yihua
, p. 9357 - 9369 (2015/01/09)
Histone deacetylases (HDACs) are one of the most promising drug targets for cancer therapy, and since more than 90% of all cancer-related deaths are associated with tumor metastasis, developing strategies to inhibit tumor metastasis while retaining anti-t
Oxo/imido heterometathesis of N-sulfinylamines and carbonyl compounds catalyzed by silica-supported vanadium oxochloride
Zhizhko, Pavel A.,Zhizhin, Anton A.,Zarubin, Dmitry N.,Ustynyuk, Nikolai A.,Lemenovskii, Dmitry A.,Shelimov, Boris N.,Kustov, Leonid M.,Tkachenko, Olga P.,Kirakosyan, Gayane A.
scheme or table, p. 108 - 118 (2011/11/14)
A series of silica-supported vanadium oxo complexes has been prepared via water-free grafting VOCl3 onto the silica surface. The obtained materials have been characterized with Raman, diffuse reflectance FTIR (DRIFT) and UV-vis, 51V
