Structure-Based Identification of Aporphines with Selective 5-HT2A Receptor-Binding Activity
Version of Record online: 14 NOV 2012
© 2012 John Wiley & Sons A/S
Chemical Biology & Drug Design
Volume 81, Issue 2, pages 250–256, February 2013
How to Cite
Munusamy, V., Yap, B. K., Buckle, M. J. C., Doughty, S. W. and Chung, L. Y. (2013), Structure-Based Identification of Aporphines with Selective 5-HT2A Receptor-Binding Activity. Chemical Biology & Drug Design, 81: 250–256. doi: 10.1111/cbdd.12069
- Issue online: 10 JAN 2013
- Version of Record online: 14 NOV 2012
- Accepted manuscript online: 5 OCT 2012 11:21AM EST
- Received 24 July 2012, revised 24 September 2012 and accepted for publication 26 September 2012
Figure S1. Sequence alignment between the aminoacid sequences of the rat and human 5-HT1A,5-HT2A, D1 and D2 receptors.
Table S1. Binding energies and ligand-receptorinteractions for a set of known ligands with the rat5-HT2A receptor model.
|cbdd12069_sm_TableS1-FigS1.doc||2675K||Supporting info item|
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