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Inhibitory effects of 6-O-acylated L-ascorbic acids possessing a straight- or branched-acyl chain on Epstein-Barr virus activation.
Uesato, S; Kitagawa, Y; Kaijima, T; Tokuda, H; Okuda, M; Mou, X Y; Mukainaka, T; Nishino, H.
Affiliation
  • Uesato S; Department of Biotechnology, Faculty of Engineering, Kansai University, Suita, 564-8680, Osaka, Japan. uesato@ipcku.kansai-u.ac.jp
Cancer Lett ; 166(2): 143-6, 2001 May 26.
Article in En | MEDLINE | ID: mdl-11311486
6-O-Acylated L-ascorbic acids possessing a straight- or branched-acyl chain of varying length from C(4) to C(18) have been synthesized and evaluated their anti-tumor promoting effects on the activation of the Epstein-Barr virus early antigen. The derivatives having a straight- or branched-acyl chain of C(6) to C(11) carbon atoms exhibited marked effects.
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Collection: 01-internacional Database: MEDLINE Main subject: Ascorbic Acid / Anticarcinogenic Agents / Herpesvirus 4, Human / Antioxidants Language: En Journal: Cancer Lett Year: 2001 Document type: Article Affiliation country: Japan Country of publication: Ireland
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Collection: 01-internacional Database: MEDLINE Main subject: Ascorbic Acid / Anticarcinogenic Agents / Herpesvirus 4, Human / Antioxidants Language: En Journal: Cancer Lett Year: 2001 Document type: Article Affiliation country: Japan Country of publication: Ireland