2.23
[]. A W Girotti, et al. Lipid peroxidation in erythrocyte membranes: cholesterol product analysis in photosensitized and xanthine oxidase-catalyzed reactions. Lipids. 87 Jun;22(6):4-8.
[2]. Alfred O Inman, et al. Percutaneous absorption of 2,6-di-tert-butyl-4-nitrophenol (DBNP) in isolated perfused porcine skin. Toxicol In Vitro. 23 Jun;7(3):28-2.
[3]. Cynthia D Selassie, et al. Cellular apoptosis and cytotoxicity of phenolic compounds: a quantitative structure-activity relationship study. J Med Chem. 25 Nov 7;48(23):7234-42.
[4]. G Haeseler, et al. High-affinity block of voltage-operated rat IIA neuronal sodium channels by 2,6 di-tert-butylphenol, a propofol analogue. Eur J Anaesthesiol. 23 Mar;2(3):22-4.
[5]. Masahiro Ogata, et al. Antioxidant activity of propofol and related monomeric and dimeric compounds. Chem Pharm Bull (Tokyo). 25 Mar;53(3):344-6.
H35-H4
P264-P273-P28-P32+P352-P362+P364
GHS7,GHS
377