Pyrazolo[1,5-a]pyrimidines as orally available inhibitors of cyclin-dependent kinase 2

Typeset version

 

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  - 
@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}
}
AUTHORSParuch, 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.
YEAR2007
MONTHNovember
JOURNAL_CODEBioorg Med Chem Lettbioorg Med Chem Lett
TITLEPyrazolo[1,5-a]pyrimidines as orally available inhibitors of cyclin-dependent kinase 2
STATUSValidated
TIMES_CITED()
SEARCH_KEYWORD
VOLUME17
ISSUE2222
START_PAGE6220
END_PAGE3
ABSTRACTProperly 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.
PUBLISHER_LOCATION
ISBN_ISSN0960-894X (Print) 0960-89
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