Larisch B, Pischetsrieder M, Severin T (1997)
Publication Type: Journal article
Publication year: 1997
Publisher: Elsevier
Book Volume: 7
Pages Range: 2681-2686
DOI: 10.1016/S0960-894X(97)10056-7
L-Ascorbic acid (AA) was incubated with guanosine under physiological conditions and the reaction was monitored by HPLC-DAD. Four reaction products were isolated and identified as two pairs of diastereomers of N2-(1-Carboxyethyl)-guanosine and N2-(1-Carboxy-3-hydroxypropyl)-guanosine respectively. They were formed from AA in the presence of oxygen as well as from its degradation products L-dehydroascorbic acid and L-xylosone.
APA:
Larisch, B., Pischetsrieder, M., & Severin, T. (1997). Formation of Guanosine Adducts from L-Ascorbic Acid under Oxidative Conditions. Bioorganic & Medicinal Chemistry Letters, 7, 2681-2686. https://dx.doi.org/10.1016/S0960-894X(97)10056-7
MLA:
Larisch, Bernd, Monika Pischetsrieder, and Theodor Severin. "Formation of Guanosine Adducts from L-Ascorbic Acid under Oxidative Conditions." Bioorganic & Medicinal Chemistry Letters 7 (1997): 2681-2686.
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