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J Oleo Sci ; 62(3): 181-6, 2013.
Article in English | MEDLINE | ID: mdl-23470446

ABSTRACT

Anti-oxidative, anti-tumor-promoting, and anti-carcinogenic activities of adonirubin and adonixanthin, which are biosynthetic intermediates from ß-carotene to astaxanthin, were investigated. Both adonirubin and adonixanthin showed almost the same activities for inhibition of lipid peroxidation and quenching of singlet oxygen as those of astaxanthin. Furthermore, adonirubin and adonixanthin exhibited an inhibitory effect on Epstein-Barr virus early antigen activation in Raji cells and carcinogensis of mouse skin tumors initiated by 7,12-dimethylbenz[a]anthracene and promoted by 12-O-tetradecanoylphorbol-13-acetate.


Subject(s)
Anticarcinogenic Agents/pharmacology , Antineoplastic Agents/pharmacology , Antioxidants/pharmacology , Canthaxanthin/analogs & derivatives , Carotenoids/pharmacology , Skin Neoplasms/drug therapy , Viral Matrix Proteins/antagonists & inhibitors , 9,10-Dimethyl-1,2-benzanthracene/antagonists & inhibitors , Animals , Anticarcinogenic Agents/chemistry , Anticarcinogenic Agents/metabolism , Antineoplastic Agents/chemistry , Antineoplastic Agents/metabolism , Antioxidants/chemistry , Antioxidants/metabolism , Canthaxanthin/biosynthesis , Canthaxanthin/chemistry , Canthaxanthin/pharmacology , Carotenoids/biosynthesis , Carotenoids/chemistry , Cell Line, Tumor , Dose-Response Relationship, Drug , Drug Screening Assays, Antitumor , Female , Humans , Lipid Peroxidation/drug effects , Mice , Mice, Inbred ICR , Molecular Structure , Paracoccus/chemistry , Paracoccus/metabolism , Singlet Oxygen/chemistry , Skin Neoplasms/chemically induced , Structure-Activity Relationship , Tetradecanoylphorbol Acetate/antagonists & inhibitors
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