| Literature DB >> 27162124 |
Mathieu Cassien1, Consuelo Petrocchi1, Sophie Thétiot-Laurent1, Maxime Robin1, Emilie Ricquebourg1, Chouaib Kandouli1, Alice Asteian1, Antal Rockenbauer2, Anne Mercier1, Marcel Culcasi1, Sylvia Pietri3.
Abstract
A series of new hybrid 2-(diethoxyphosphoryl)-N-(benzylidene)propan-2-amine oxide derivatives with different aromatic substitution (PPNs) were synthesized. These molecules were evaluated for their EPR spin trapping potential on eleven different radicals and NO-donation properties in vitro, cytotoxicity and vasoprotective effect on precontracted rat aortic rings. A subfamily of the new PPNs featured an antioxidant moiety occurring in natural phenolic acids. From the experimental screening of these hydroxyphenyl- and methoxyphenyl-substituted PPNs, biocompatible nitrones 4d, and 4g-4i deriving from caffeic, gallic, ferulic and sinapic acids, which combined improved EPR probing of ROS formation, vasorelaxant action and antioxidant potency, might be potential drug candidate alternatives to PBN and its analogues.Entities:
Keywords: Antioxidant; Aortic rings relaxation; EPR spin trapping; NO donors; Phenolic acids; β-Diethoxyphosphoryl nitrones
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Year: 2016 PMID: 27162124 DOI: 10.1016/j.ejmech.2016.04.067
Source DB: PubMed Journal: Eur J Med Chem ISSN: 0223-5234 Impact factor: 6.514