发明名称 |
OLIGODEOXYRIBONUCLEOTIDES COMPRISING O<6>-BENZYLGUANINE AND THEIR USE |
摘要 |
The present invention provides a single-stranded oligodeoxyribonucleotide, which (i) comprises from about 5 to 11 bases, at least one of which is a substituted or an unsubstituted O<6>-benzylguanine, and (ii) inactivates human AGT. The present invention also provides a single-stranded oligodeoxyribonucleotide, which can inactivate a mutant human AGT, which either is not inactivated by O<6>-benzylguanine or is less inactivated by O<6>-benzylguanine than by said single-stranded oligodeoxyribonucleotide. A phosphate of the single-stranded oligodeoxyribonucleotide can be replaced by a methylphosphonate or a phosphorothioate. The present invention also provides a composition comprising such an oligodeoxyribonucleotide. In addition, the present invention provides a method of enhancing the effect of an antineoplastic alkylating agent, which alkylates the O<6> position of guanine residues in DNA, in the chemotherapeutic treatment of cancer in a mammal, which method comprises the co-administration to the mammal of a cancer-treatment effective amount of an antineoplastic alkylating agent and a chemotherapeutic treatment-enhancing amount of a present inventive oligodeoxyribonucleotide or composition thereof.
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申请公布号 |
WO9941269(A1) |
申请公布日期 |
1999.08.19 |
申请号 |
WO1999US02963 |
申请日期 |
1999.02.12 |
申请人 |
THE UNITED STATES OF AMERICA, REPRESENTED BY SECRETARY, DEPARTMENT OF HEALTH AND HUMAN SERVICES;ARCH DEVELOPMENT CORPORATION;THE PENN STATE RESEARCH FOUNDATION |
发明人 |
MOSCHEL, ROBERT, C.;PAULY, GARY, T.;PEGG, ANTHONY, E.;DOLAN, M., EILEEN |
分类号 |
C07H21/04;A61K31/175;A61K31/7115;A61P35/00;A61P43/00;C07H21/00;(IPC1-7):C07H21/00;A61K31/70 |
主分类号 |
C07H21/04 |
代理机构 |
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代理人 |
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主权项 |
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