| Literature DB >> 21500796 |
Toshihide Yamasaki1, Yuko Ito, Fumiya Mito, Kana Kitagawa, Yuta Matsuoka, Mayumi Yamato, Ken-ichi Yamada.
Abstract
Nitroxides have antioxidative activities toward lipid peroxidation, but the influence of steric factors is not known. We synthesized alkyl-substituted nitroxides at the α-position of the N-O moiety to enhance lipophilicity and the bulk effect. There was good correlation between the IC(50) and lipophilicity (log P(o/w)) of nitroxides with use of the thiobarbituric acid-reactive substances (TBARS) assay. Furthermore, an inhibitory effect on the TBARS assay was dependent upon the number and length of alkyl groups, though nitroxides had almost identical lipophilicity.Entities:
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Year: 2011 PMID: 21500796 DOI: 10.1021/jo200361p
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354