Solid-Phase Synthesis and Insights into Structure−Activity Relationships of Safinamide Analogues as Potent and Selective Inhibitors of Type B Monoamine Oxidase
Author:
Affiliation:
1. Dipartimento Farmaco-Chimico, University of Bari, Via Orabona 4, I-70125 Bari, Italy, and Newron Pharmaceuticals, Via L. Ariosto 21, Bresso, Italy
Publisher
American Chemical Society (ACS)
Subject
Drug Discovery,Molecular Medicine
Link
https://pubs.acs.org/doi/pdf/10.1021/jm070725e
Reference39 articles.
1. Enzymology of monoamine oxidase
2. Clinical Pharmacology of MAO Inhibitors: Safety and Future
3. Structure of human monoamine oxidase B, a drug target for the treatment of neurological disorders
4. Insights into the mode of inhibition of human mitochondrial monoamine oxidase B from high-resolution crystal structures
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