Discovering Isozyme-Selective Inhibitor Scaffolds of Human Carbonic Anhydrases Using Structural Alignment and De novo Drug Design Approaches
Article first published online: 26 DEC 2013
© 2013 John Wiley & Sons A/S
Chemical Biology & Drug Design
Volume 83, Issue 2, pages 247–258, February 2014
How to Cite
Xiang, F., Xiang, J., Fang, Y., Zhang, M. and Li, M. (2014), Discovering Isozyme-Selective Inhibitor Scaffolds of Human Carbonic Anhydrases Using Structural Alignment and De novo Drug Design Approaches. Chemical Biology & Drug Design, 83: 247–258. doi: 10.1111/cbdd.12234
- Issue published online: 17 JAN 2014
- Article first published online: 26 DEC 2013
- Accepted manuscript online: 1 OCT 2013 12:32PM EST
- Manuscript Accepted: 15 SEP 2013
- Manuscript Revised: 24 AUG 2013
- Manuscript Received: 19 JUL 2013
- Doctoral Foundation of Huanggang Normal University. Grant Number: 2011CD220
- Natural Science Funds for Distinguished Young Scholars of Hubei Province of China. Grant Number: 2010CDA097
- New Century Talents Support Program of the Ministry of Education of China. Grant Number: NCET110172
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