| 摘要 |
<p>O6-Benzylated guanine guanosine and 2'-deoxyguanosine compounds of formula (I), wherein Z is hydrogen, (α) or (β), and R is a benzyl group or a substituted benzyl group, cause a depletion of O6-alkylguanine-DNA alkyltransferase (AGT) activity in mammalian cells. These compounds may be administered to a host so as to reduce AGT levels in tumor cells of the host in order to increase host responsiveness to anti-neoplastic alkylating agents, including chloroethylating agents, such as chloroethylnitrosoureas, for chemotherapeutic treatment of a number of neoplasms.</p> |
