Literature DB >> 16272727

Superoxide anion-scavenging effect of 2-amino-1,3-selenazoles.

Akihiro Sekiguchi1, Atsuyoshi Nishina, Hirokazu Kimura, Ryo-hei Fukumoto, Koichi Kanoh, Hideharu Ishihara, Mamoru Koketsu.   

Abstract

We investigated the superoxide anion scavenging effects of thirteen 2-amino-1,3-selenazoles using a highly sensitive quantitative chemiluminescence method. At 166 microM, the 2-amino-1,3-selenazoles scavenged in the range of 14.3 to 96.7% of O2-. 2-Piperidino-1,3-selenazole and 4-phenyl-2-piperidino-1,3-selenazole exhibited the strongest superoxide anion-scavenging activity among the 2-amino-1,3-selenazoles. The 50% inhibitory concentrations (IC50) of 2-piperidino-1,3-selenazole and 4-phenyl-2-piperidino-1,3-selenazole were determined to be 4.03 microM and 92.6 microM, respectively. Thus, these compounds acted in vitro as effective O2- scavengers.

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Year:  2005        PMID: 16272727     DOI: 10.1248/cpb.53.1439

Source DB:  PubMed          Journal:  Chem Pharm Bull (Tokyo)        ISSN: 0009-2363            Impact factor:   1.645


  1 in total

1.  Synthesis and Single Crystal Structures of Substituted-1,3-Selenazol-2-amines.

Authors:  Guoxiong Hua; Junyi Du; Alexandra M Z Slawin; J Derek Woollins
Journal:  Molecules       Date:  2016-12-29       Impact factor: 4.411

  1 in total

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