Handlon A L, Oppenheimer N J
Department of Pharmaceutical Chemistry, University of California, San Francisco 94143.
Pharm Res. 1988 May;5(5):297-9. doi: 10.1023/a:1015926720740.
The ability of thiols to reduce 3'-azidothymidine (AZT) to 3'-aminothymidine has been investigated. Incubation with glutathione, dithiothreitol (DTT), or mercaptoethanol at pH 7.2 and 37 degrees C leads to quantitative reduction of the azido moiety to an amine. The reaction is first order in AZT and first order in reducing agent (mono- or dithiol). The second-order rate constants are 2.77 x 10(-3), 6.55 x 10(-5), and 6.35 x 10(-6) M-1 sec-1 for the dithiothreitol, glutathione, and mercaptoethanol reductions, respectively. The thiol reduction of alkyl azide to amine under mild conditions is a synthetic method particularly suitable for water-soluble azido compounds that are sensitive to catalytic hydrogenation. The potential for the mono- or dithiol-mediated reduction of alkyl azides under biological conditions must be considered when conducting studies of azido drugs.
