IRIS publication 280546817
Pyrazolo[1,5-a]pyrimidines as orally available inhibitors of cyclin-dependent kinase 2
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TY - JOUR - Paruch, K.,Dwyer, M. P.,Alvarez, C.,Brown, C.,Chan, T. Y.,Doll, R. J.,Keertikar, K.,Knutson, C.,McKittrick, B.,Rivera, J.,Rossman, R.,Tucker, G.,Fischmann, T. O.,Hruza, A.,Madison, V.,Nomeir, A. A.,Wang, Y.,Lees, E.,Parry, D.,Sgambellone, N.,Seghezzi, W.,Schultz, L.,Shanahan, F.,Wiswell, D.,Xu, X.,Zhou, Q.,James, R. A.,Paradkar, V. M.,Park, H.,Rokosz, L. R.,Stauffer, T. M.,Guzi, T. J. - 2007 - November - Bioorg Med Chem Lettbioorg Med Chem Lett - Pyrazolo[1,5-a]pyrimidines as orally available inhibitors of cyclin-dependent kinase 2 - Validated - () - 17 - 2222 - 6220 - 3 - Properly substituted pyrazolo[1,5-a]pyrimidines are potent and selective CDK2 inhibitors. Compound 15j is orally available and showed efficacy in a mouse A2780 xenograft model.Properly substituted pyrazolo[1,5-a]pyrimidines are potent and selective CDK2 inhibitors. Compound 15j is orally available and showed efficacy in a mouse A2780 xenograft model. - 0960-894X (Print) 0960-89 DA - 2007/11 ER -
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@article{V280546817, = {Paruch, K. and Dwyer, M. P. and Alvarez, C. and Brown, C. and Chan, T. Y. and Doll, R. J. and Keertikar, K. and Knutson, C. and McKittrick, B. and Rivera, J. and Rossman, R. and Tucker, G. and Fischmann, T. O. and Hruza, A. and Madison, V. and Nomeir, A. A. and Wang, Y. and Lees, E. and Parry, D. and Sgambellone, N. and Seghezzi, W. and Schultz, L. and Shanahan, F. and Wiswell, D. and Xu, X. and Zhou, Q. and James, R. A. and Paradkar, V. M. and Park, H. and Rokosz, L. R. and Stauffer, T. M. and Guzi, T. J. }, = {2007}, = {November}, = {Bioorg Med Chem Lettbioorg Med Chem Lett}, = {Pyrazolo[1,5-a]pyrimidines as orally available inhibitors of cyclin-dependent kinase 2}, = {Validated}, = {()}, = {17}, = {2222}, pages = {6220--3}, = {{Properly substituted pyrazolo[1,5-a]pyrimidines are potent and selective CDK2 inhibitors. Compound 15j is orally available and showed efficacy in a mouse A2780 xenograft model.Properly substituted pyrazolo[1,5-a]pyrimidines are potent and selective CDK2 inhibitors. Compound 15j is orally available and showed efficacy in a mouse A2780 xenograft model.}}, issn = {0960-894X (Print) 0960-89}, source = {IRIS} }
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AUTHORS | Paruch, K.,Dwyer, M. P.,Alvarez, C.,Brown, C.,Chan, T. Y.,Doll, R. J.,Keertikar, K.,Knutson, C.,McKittrick, B.,Rivera, J.,Rossman, R.,Tucker, G.,Fischmann, T. O.,Hruza, A.,Madison, V.,Nomeir, A. A.,Wang, Y.,Lees, E.,Parry, D.,Sgambellone, N.,Seghezzi, W.,Schultz, L.,Shanahan, F.,Wiswell, D.,Xu, X.,Zhou, Q.,James, R. A.,Paradkar, V. M.,Park, H.,Rokosz, L. R.,Stauffer, T. M.,Guzi, T. J. | ||
YEAR | 2007 | ||
MONTH | November | ||
JOURNAL_CODE | Bioorg Med Chem Lettbioorg Med Chem Lett | ||
TITLE | Pyrazolo[1,5-a]pyrimidines as orally available inhibitors of cyclin-dependent kinase 2 | ||
STATUS | Validated | ||
TIMES_CITED | () | ||
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VOLUME | 17 | ||
ISSUE | 2222 | ||
START_PAGE | 6220 | ||
END_PAGE | 3 | ||
ABSTRACT | Properly substituted pyrazolo[1,5-a]pyrimidines are potent and selective CDK2 inhibitors. Compound 15j is orally available and showed efficacy in a mouse A2780 xenograft model.Properly substituted pyrazolo[1,5-a]pyrimidines are potent and selective CDK2 inhibitors. Compound 15j is orally available and showed efficacy in a mouse A2780 xenograft model. | ||
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ISBN_ISSN | 0960-894X (Print) 0960-89 | ||
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