Novel Reversible Monoamine Oxidase A Inhibitors: Highly Potent and Selective 3-(1H-Pyrrol-3-yl)-2-oxazolidinones-Reference-Cited by-同舟云学术

Novel Reversible Monoamine Oxidase A Inhibitors: Highly Potent and Selective 3-(1H-Pyrrol-3-yl)-2-oxazolidinones

Published:2011-11-07 Issue:23 Volume:54 Page:8228-8232
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Valente Sergio¹,Tomassi Stefano¹,Tempera Giampiero²,Saccoccio Stefania²,Agostinelli Enzo²,Mai Antonello¹

Affiliation:

1. Dipartimento di Chimica e Tecnologie del Farmaco, Istituto Pasteur, Fondazione Cenci Bolognetti, Sapienza Università di Roma, Piazzale Aldo Moro 5, 00185 Roma, Italy

2. Dipartimento di Scienze Biochimiche Rossi-Fanelli and Istituto di Biologia e Patologia Molecolare del CNR, Istituto Pasteur, Fondazione Cenci Bolognetti, Sapienza Università di Roma, Piazzale Aldo Moro 5, 00185 Roma, Italy

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm201011x

Reference29 articles.

1. Biochemistry and genetics of monoamine oxidase

2. Structure of human monoamine oxidase B, a drug target for the treatment of neurological disorders

3. Insights into the mode of inhibition of human mitochondrial monoamine oxidase B from high-resolution crystal structures

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