专利号:US-6531477-B1 优先权日:1998-10-13 标 题:6-substituted pyrazolo [3,4-d] pyrimidin-4-ones useful as cyclin dependent kinase inhibitors 发明人:MARKWALDER JAY A; SEITZ STEVEN P; SHERK SUSAN R 权利人:DU PONT PHARM CO 摘要:The present invention relates to the synthesis of a novel class of pyrazolo[3,4-d]pyrimidin-4-ones of formula (I), alternatively represented by the tautomer (II):that are potent inhibitors of the class of enzymes known as cyclin dependent kinases, which relate to the catalytic subunits cyclin dependent kinase 1-8 and their regulatory subunits know as cyclins A-H, K, N, and T.This invention also provides a novel method of treating cancer or other proliferative diseases by administering a therapeutically effective amount of one of these compounds or a pharmaceutically acceptable salt form thereof. Alternatively, one can treat cancer or other proliferative diseases by administering a therapeutically effective combination of one of the compounds of the present invention and one or more other known anti-cancer or anti-proliferative agents.
专利号:US-6559152-B2 优先权日:1998-10-13 标 题 :6-substituted pyrazolo[3,4-d]pyrimidin-4-ones useful as cyclin dependent kinase inhibitors 发明人:MARKWALDER JAY A; SEITZ STEVEN P; SHERK SUSAN R 权利人:DU PONT PHARM CO 摘要:The present invention relates to the synthesis of a novel class of pyrazolo[3,4-d]pyrimidin-4-ones of formula (I), alternatively represented by the tautomer (II):that are potent inhibitors of the class of enzymes known as cyclin dependent kinases, which relate to the catalytic subunits cyclin dependent kinase 1-8 and their regulatory subunits know as cyclins A-H, K, N, and T.This invention also provides a novel method of treating cancer or other proliferative diseases by administering a therapeutically effective amount of one of these compounds or a pharmaceutically acceptable salt form thereof. Alternatively, one can treat cancer or other proliferative diseases by administering a therapeutically effective combination of one of the compounds of the present invention and one or more other known anti-cancer or anti-proliferative agents.
参考文献:10.1055/s-0034-1378274 摘要:Yoshimura F, Tanino K, Abe T. Nucleophilic Addition Reactions of Nitriles to Nitrones under Mild Silylation Conditions. Synlett. 2014 Jun 24;25(13):1863–8. doi: 10.1055/s-0034-1378274. 参考文献:10.1007/s11426-024-2000-3 摘要:Pan M, Zhang G, Ma H, Cheng X, Li J, Zhang W. In situ thermoresponsive supramolecular assembly for switchable circularly polarized luminescence. Sci. China Chem. 2024 May 27;67(7):2362–72. doi: 10.1007/s11426-024-2000-3.