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Found 2 publications
Structure-based design of 2,6,7-trisubstituted-7H-pyrrolo[2,3-d]pyrimidines as Aurora kinases inhibitors.
Journal: Bioorganic & medicinal chemistry letters
Published: February 17, 2012
Synthesis, SAR and biological evaluation of 1,6-disubstituted-1H-pyrazolo[3,4-d]pyrimidines as dual inhibitors of Aurora kinases and CDK1.
Journal: Bioorganic & medicinal chemistry letters
Published: October 26, 2011
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Last Updated: 09/26/2026