12 articles for A Uri
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
Data
Article Title
Organization
Fluorescent photoaffinity probes for mitotic protein kinase Aurora A.
University of Tartu
Conjugates of 5-isoquinolinesulfonylamides and oligo-D-arginine possess high affinity and selectivity towards Rho kinase (ROCK).
University of Tartu
Adenosine-5'-carboxylic acid peptidyl derivatives as inhibitors of protein kinases.
Tartu University
Effect of the structure of adenosine mimic of bisubstrate-analog inhibitors on their activity towards basophilic protein kinases.
University of Tartu
Carbocyclic 3'-deoxyadenosine-based highly potent bisubstrate-analog inhibitor of basophilic protein kinases.
University of Tartu
Conjugation of adenosine and hexa-(D-arginine) leads to a nanomolar bisubstrate-analog inhibitor of basophilic protein kinases.
Institute of Organic and Bioorganic Chemistry
Construction of Covalent Bisubstrate Inhibitor of Protein Kinase Reacting with Cysteine Residue at Substrate-Binding Site.
University of Tartu
Thiazole- and selenazole-comprising high-affinity inhibitors possess bright microsecond-scale photoluminescence in complex with protein kinase CK2.
University of Tartu
Oligo-aspartic acid conjugates with benzo[c][2,6]naphthyridine-8-carboxylic acid scaffold as picomolar inhibitors of CK2.
University of Tartu
Structural determinants of CDK4 inhibition and design of selective ATP competitive inhibitors.
Cyclacel