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Tempace and troxyl-novel synthesized 2,2,6,6-tetramethylpiperidine derivatives as antioxidants and radioprotectors.

Biochemistry and molecular biology international (1996-12-01)
D Metodiewa, J Skolimowski, S Karolczak
RÉSUMÉ

Two novel 2,2,6,6-tetramethylpiperidine derivatives (Tempace and Troxyl) were synthesized and their capacity to act as scavengers of superoxide, inhibitors of iron and ascorbate-driven Fenton reaction and radioprotectors was tested. The possibility for one-electron oxidation of novel compounds by heme-ferryl species was also examined. The results clearly indicate that Tempace and Troxyl are acting as promising antioxidants and radioprotectors thus providing a base for further investigations and pharmacological applications.

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Sigma-Aldrich
4-Acetamido-TEMPO, free radical, 97%
Sigma-Aldrich
4-Acetamido-2,2,6,6-tetramethylpiperidine 1-oxyl, purum, ≥98.0% (HPLC)