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Anti-tumor promoting effect of glycosides from Prunus persica seeds.

Abstract
Four minor components, along with the major cyanogenic glycosides, amygdalin and prunasin, were isolated from Prunus persica seeds (Persicae Semen; Tounin), and characterized as mandelic acid glycosides (beta-gentiobioside and beta-D-glucoside) and benzyl alcohol glycosides (beta-gentiobioside and beta-D-glucoside). The anti-tumor promoting activity of these compounds was examined in both in vitro and in vivo assays. All of the compounds significantly inhibited the Epstein-Barr virus early antigen activation induced by tumor promoter. In addition, they produced a delay of two-stage carcinogenesis on mouse skin that was comparable in potency to (-)-epigallocatechin gallate from green tea. Structure-activity relationships indicated that a substituent at the benzylic position with glycosidic linkage affected the in vitro and in vivo activities with an order of enhancing potency, CN<COOH<H.
AuthorsToshiyuki Fukuda, Hideyuki Ito, Teruo Mukainaka, Harukuni Tokuda, Hoyoku Nishino, Takashi Yoshida
JournalBiological & pharmaceutical bulletin (Biol Pharm Bull) Vol. 26 Issue 2 Pg. 271-3 (Feb 2003) ISSN: 0918-6158 [Print] Japan
PMID12576693 (Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Antigens, Viral
  • Antineoplastic Agents
  • Carcinogens
  • Epstein-Barr virus early antigen
  • Glycosides
  • Plant Extracts
Topics
  • Animals
  • Antigens, Viral (metabolism)
  • Antineoplastic Agents (chemistry, isolation & purification, pharmacology, therapeutic use)
  • Carcinogens (antagonists & inhibitors, metabolism)
  • Female
  • Glycosides (chemistry, isolation & purification, pharmacology, therapeutic use)
  • Humans
  • Mice
  • Mice, Inbred ICR
  • Plant Extracts (chemistry, isolation & purification, pharmacology, therapeutic use)
  • Prunus
  • Seeds
  • Skin Neoplasms (drug therapy, metabolism)

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