about
Solid-phase synthesis of trisubstituted benzo[1,4]-diazepin-5-one derivatives.Trisubstituted pyrazolopyrimidines as novel angiogenesis inhibitors.2,6,9-Trisubstituted purines as CRK3 kinase inhibitors with antileishmanial activity in vitro.Characterization of a Pyrazolo[4,3-d]pyrimidine Inhibitor of Cyclin-Dependent Kinases 2 and 5 and Aurora A With Pro-Apoptotic and Anti-Angiogenic Activity In Vitro.A novel series of highly potent 2,6,9-trisubstituted purine cyclin-dependent kinase inhibitors.A Stepwise Approach for the Synthesis of Folic Acid Conjugates with Protein Kinase Inhibitors.Trisubstituted purine inhibitors of PDGFRα and their antileukemic activity in the human eosinophilic cell line EOL-1.Synthesis and kinase inhibitory activity of new sulfonamide derivatives of pyrazolo[4,3-e][1,2,4]triazines.Preparation, characterization and biological activity of C8-substituted cytokinins.Discovery of N2-(4-Amino-cyclohexyl)-9-cyclopentyl- N6-(4-morpholin-4-ylmethyl-phenyl)- 9H-purine-2,6-diamine as a Potent FLT3 Kinase Inhibitor for Acute Myeloid Leukemia with FLT3 Mutations.Synthesis and in vitro biological evaluation of 2,6,9-trisubstituted purines targeting multiple cyclin-dependent kinases.LC-MS/MS method for determination of cyclin-dependent kinase inhibitors, BP-14 and BP-20, and its application in pharmacokinetic study in rat.
P50
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P50
name
Tomáš Gucký
@ast
Tomáš Gucký
@en
Tomáš Gucký
@nl
type
label
Tomáš Gucký
@ast
Tomáš Gucký
@en
Tomáš Gucký
@nl
prefLabel
Tomáš Gucký
@ast
Tomáš Gucký
@en
Tomáš Gucký
@nl