151166-75-5Relevant articles and documents
Peroxynitrite generation from a NO-releasing nitrobenzene derivative in response to photoirradiation
Ieda, Naoya,Nakagawa, Hidehiko,Horinouchi, Taeko,Peng, Tao,Yang, Dan,Tsumoto, Hiroki,Suzuki, Takayoshi,Fukuhara, Kiyoshi,Miyata, Naoki
supporting information; experimental part, p. 6449 - 6451 (2011/06/27)
Photocontrollable ONOO- generation from a nitrobenzene derivative was demonstrated. The designed compound released NO in response to photoirradiation, and the resulting semiquinone reduced molecular oxygen to generate O2-; reaction of the two generated ONOO -, as confirmed with an ONOO- fluorescent probe, HKGreen-3.
Development of a new class of potential antiatherosclerosis agents: NO-donor antioxidants
Cena, Clara,Boschi, Donatella,Tron, Gian Cesare,Chegaev, Kostantin,Lazzarato, Loretta,Stilo, Antonella Di,Aragno, Manuela,Fruttero, Roberta,Gasco, Alberto
, p. 5971 - 5974 (2007/10/03)
A new class of NO-donor phenol derivatives is described. The products were obtained by joining appropriate phenols with either nitrooxy or 3-phenylsulfonylfuroxan-4-yloxy moieties. All the compounds proved to inhibit the ferrous salt/ascorbate induced lip
3,4,5-trisubstituted aryl nitrone compounds, pharmaceutical compositions containing the same and methods for treating inflammation
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Page column 20-21, (2008/06/13)
Disclosed are 3,4,5-trisubstituted aryl nitrone compounds and pharmaceutical compositions containing such compounds. The 3,4,5-trisubstituted aryl nitrone compounds have the formula: where R1-R4are as defined in the specification. The disclosed compositions are useful as therapeutics for inflammation-related conditions in mammals, such as arthritis, and as analytical reagents for detecting free radicals.
