Mandelonitrile β-Glucuronide: Synthesis and Characterization

Mandelonitrile β-glucuronide, the compound patented as Laetrile ®, has been synthesized from rabbit liver uridine diphosphate-glucuronosyl transferase immobilized on beaded sepharose, has been analyzed by thin-layer chromatography, nuclear magnetic resonance, and gas chromatography-mass spectrometry...

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Veröffentlicht in:Science (American Association for the Advancement of Science) 1977-11, Vol.198 (4317), p.625-627
Hauptverfasser: Fenselau, Catherine, Pallante, Sharon, Batzinger, Robert P., Benson, Walter R., Barron, Robert P., Sheinin, Eric B., Maienthal, Millard
Format: Artikel
Sprache:eng
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Zusammenfassung:Mandelonitrile β-glucuronide, the compound patented as Laetrile ®, has been synthesized from rabbit liver uridine diphosphate-glucuronosyl transferase immobilized on beaded sepharose, has been analyzed by thin-layer chromatography, nuclear magnetic resonance, and gas chromatography-mass spectrometry, and has been tested for cytotoxicity and mutagenic activity with Salmonella typhimurium strains TA 98 and TA 100. Several commercial laetrile preparations contained no glucuronide; they contained amygdalin and neoamygdalin instead. Mandelonitrile, mandelonitrile glucuronide, and a mixture of amygdalin and neoamygdalin were each found to be mutagenic.
ISSN:0036-8075
1095-9203
DOI:10.1126/science.335509