| Literature DB >> 22280820 |
Loredana Salerno1, Maria N Modica, Giuseppe Romeo, Valeria Pittalà, Maria A Siracusa, Maria E Amato, Rosaria Acquaviva, Claudia Di Giacomo, Valeria Sorrenti.
Abstract
We previously described a series of imidazole-based inhibitors substituted at N-1 with an arylethanone chain as interesting inhibitors of neuronal nitric oxide synthase (nNOS), endowed with good selectivity vs endothelial nitric oxide synthase (eNOS). As a follow up of these studies, several analogs characterized by the presence of substituted imidazoles or other mono or bicyclic nitrogen-containing heterocycles instead of simple imidazole were synthesized, and their biological evaluation as in vitro inhibitors of both nNOS and eNOS is described herein. Most of these compounds showed improved nNOS and eNOS inhibitory activity with respect to reference inhibitors. Selected compounds were also tested to analyze their antioxidant properties. Some of them displayed good capacity to scavenge free radicals and ability to reduce lipid peroxidation. Copyright ÂEntities:
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Year: 2012 PMID: 22280820 DOI: 10.1016/j.ejmech.2012.01.002
Source DB: PubMed Journal: Eur J Med Chem ISSN: 0223-5234 Impact factor: 6.514