Title of article
Formation of 8-oxo-7,8-dihydro-2′-deoxyguanosine under anaerobic conditions by reductively activated nitro 5-deazaflavin derivatives
Author/Authors
Yuji Mikata، نويسنده , , Maki Kishigami، نويسنده , , Mamiko Nishida، نويسنده , , Shigenobu Yano، نويسنده , , Tetsuji Kawamoto، نويسنده , , Yoshihiro Ikeuchi، نويسنده , , Fumio Yoneda، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 1999
Pages
4
From page
2141
To page
2144
Abstract
Electrolytically reduced 6- and 8-nitro-5-deazaflavin derivatives have been found to interact to react specifically with guanine base by means of cyclic voltammetry. Electrolytic reductions 6- and 8-nitro-5-deazaflavin derivatives in the presence of the 2′-deoxyguanosine under anaerobic conditions resulted in prominent formation of 8-oxo-7,8-dihydro-2′-deoxyguanosine.
Journal title
Bioorganic & Medicinal Chemistry Letters
Serial Year
1999
Journal title
Bioorganic & Medicinal Chemistry Letters
Record number
790300
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