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

3-(1H-Pyrrol-1-yl)-2-oxazolidinones as Reversible, Highly Potent, and Selective Inhibitors of Monoamine Oxidase Type A

Published:2002-02-06 Issue:6 Volume:45 Page:1180-1183
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Mai Antonello¹,Artico Marino¹,Esposito Monica¹,Sbardella Gianluca¹,Massa Silvio¹,Befani Olivia¹,Turini Paola¹,Giovannini Valentina¹,Mondovì Bruno¹

Affiliation:

1. Dipartimento di Studi Farmaceutici, Università degli Studi di Roma “La Sapienza”, P.le A. Moro 5, 00185 Roma, Italy, Dipartimento di Scienze Farmaceutiche, Università degli Studi di Salerno, via Ponte Don Melillo, 84084 Fisciano (SA), Italy, Dipartimento Farmaco Chimico Tecnologico, Università degli Studi di Siena, via Aldo Moro, 53100 Siena, Italy, and Dipartimento di Scienze Biochimiche “A. Rossi Fanelli” and Centro di Biologia Molecolare del CNR, Università degli Studi di Roma “La Sapienza”, P.le A....

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm015578d

Reference31 articles.

1. The Covalently-Bound Flavin of Hepatic Monoamine Oxidase. 1. Isolation and Sequence of a Flavin Peptide and Evidence for Binding at the 8alpha Position

2. Selective inhibitors of monoamine oxidase (MAO-A and MAO-B) as probes of its catalytic site and mechanism

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