209 results on '"Bretner, Maria"'
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2. Synthesis of novel proxyphylline derivatives with dual Anti-Candida albicans and anticancer activity
3. Synthesis of novel polybrominated benzimidazole derivatives—potential CK2 inhibitors with anticancer and proapoptotic activity
4. Synthesis of novel chiral TBBt derivatives with hydroxyl moiety. Studies on inhibition of human protein kinase CK2α and cytotoxicity properties
5. Synthesis of polybrominated benzimidazole and benzotriazole derivatives containing a tetrazole ring and their cytotoxic activity
6. Studies on the chemoenzymatic synthesis of (R)- and (S)-methyl 3-aryl-3-hydroxypropionates: the influence of toluene-pretreatment of lipase preparations on enantioselective transesterifications
7. Chemical proteomics and functional proteomics strategies for protein kinase inhibitor validation and protein kinase substrate identification: Applications to protein kinase CK2
8. Functional proteomics strategy for validation of protein kinase inhibitors reveals new targets for a TBB-derived inhibitor of protein kinase CK2
9. Synthesis of new optically pure tetrabromobenzotriazole derivatives via lipase-catalyzed transesterification
10. Casein kinase II-mediated phosphorylation of general repressor Maf1 triggers RNA polymerase III activation
11. Interaction with 2(4)-Thio-5-Fluoro-dUMP of Thymidylate Synthases with Differing Sensitivities to 5-Fluoro-dUMP
12. Studies on the anti-hepatitis C virus activity of newly synthesized tropolone derivatives: Identification of NS3 helicase inhibitors that specifically inhibit subgenomic HCV replication
13. Synthesis of new analogs of benzotriazole, benzimidazole and phthalimide—potential inhibitors of human protein kinase CK2
14. Synthesis of Novel Acyl Derivatives of 3-(4,5,6,7-Tetrabromo-1H-benzimidazol-1-yl)propan-1-ols—Intracellular TBBi-Based CK2 Inhibitors with Proapoptotic Properties
15. Design and synthesis of CK2 inhibitors
16. Enzymatic activity with an incomplete catalytic spine: insights from a comparative structural analysis of human CK2α and its paralogous isoform CK2α′
17. Isoform specific inhibition of human protein kinase CK2α and CK2α’ by an indenoindole derivative
18. New insight into nucleo α-amino acids – Synthesis and SAR studies on cytotoxic activity of β-pyrimidine alanines
19. A competition between hydrophobic and electrostatic interactions in protein–ligand systems. Binding of heterogeneously halogenated benzotriazoles by the catalytic subunit of human protein kinase CK2
20. Formylation of a metathesis-derivedansa[4]-ferrocene: a simple route to anticancer organometallics
21. New inhibitors of protein kinase CK2, analogues of benzimidazole and benzotriazole
22. Tetrabromobenzotriazole (TBBt) and tetrabromobenzimidazole (TBBz) as selective inhibitors of protein kinase CK2: Evaluation of their effects on cells and different molecular forms of human CK2
23. Synthesis and activity of 1 H-benzimidazole and 1 H-benzotriazole derivatives as inhibitors of Acanthamoeba castellanii
24. Diacritic Binding of an Indenoindole Inhibitor by CK2 alpha Paralogs Explored by a Reliable Path to Atomic Resolution CK2 alpha ' Structures
25. Halogenated benzimidazoles and benzotriazoles as inhibitors of the NTPase/helicase activities of hepatitis C and related viruses
26. Simultaneous Inhibition of Protein Kinase CK2 and Dihydrofolate Reductase Results in Synergistic Effect on Acute Lymphoblastic Leukemia Cells
27. Human dihydrofolate reductase is a substrate of protein kinase CK2α
28. Diacritic Binding of an Indenoindole Inhibitor by CK2α Paralogs Explored by a Reliable Path to Atomic Resolution CK2α′ Structures
29. Potential bioisosteres of β-uracilalanines derived from 1H-1,2,3-triazole-C-carboxylic acids
30. Formylation of a metathesis-derived ansa[4]-ferrocene: a simple route to anticancer organometallics.
31. Effect of Simultaneous Inhibition of Protein Kinase CK2 and Thymidylate Synthase in Leukemia and Breast Cancer Cells
32. Experimental ([super 13]C NMR) and theoretical (ab initio molecular orbital calculations) studies on the prototropic tautomerism of benzotriazole and some derivatives symmetrically substituted on the benzene ring
33. Synthesis, in vitro antiproliferative activity and kinase profile of new benzimidazole and benzotriazole derivatives
34. Lipase-Catalyzed Kinetic Resolution of Novel Antifungal N -Substituted Benzimidazole Derivatives
35. Thermodynamic parameters for binding of some halogenated inhibitors of human protein kinase CK2
36. An Unbiased Evaluation of CK2 Inhibitors by Chemoproteomics: Characterization of Inhibitor Effects on CK2 and Identification of Novel Inhibitor Targets
37. Synthesis of 4,5,6,7-Tetrabromo-1H-benzimidazole Derivatives
38. Enzymatic activity with an incomplete catalytic spine: insights from a comparative structural analysis of human CK2 alpha and its paralogous isoform CK2 alpha'
39. Synthesis and in vitro Antibacterial Activity of 5-Halogenomethylsulfonyl- Benzimidazole and Benzotriazole Derivatives
40. Unbiased Functional Proteomics Strategy for Protein Kinase Inhibitor Validation and Identification of bona fide Protein Kinase Substrates: Application to Identification of EEF1D as a Substrate for CK2
41. Structure of the Human Protein Kinase CK2 Catalytic Subunit CK2α′ and Interaction Thermodynamics with the Regulatory Subunit CK2β
42. An Unbiased Evaluation of CK2 Inhibitors by Chemoproteomics
43. Experimental (13C NMR) and Theoretical (ab Initio Molecular Orbital Calculations) Studies on the Prototropic Tautomerism of Benzotriazole and Some Derivatives Symmetrically Substituted on the Benzene Ring
44. Synthesis of 4,5,6,7-Tetrabromo-1 H-benzimidazole Derivatives.
45. Nuclear Export of S6K1 II Is Regulated by Protein Kinase CK2 Phosphorylation at Ser-17
46. Searching for a new anti-HCV therapy: Synthesis and properties of tropolone derivatives
47. Different properties of four molecular forms of protein kinase CK2 from Saccharomyces cerevisiae.
48. Synthesis and Biological Activity of 1H-benzotriazole and 1H-benzimidazole Analogues — Inhibitors of the NTPase/Helicase of HCV and of Some Related Flaviviridae
49. Corrigendum to “Synthesis and activity of 1H-benzimidazole and 1H-benzotriazole derivatives as inhibitors of Acanthamoeba castellanii” [Bioorg. Med. Chem. 12 (2004) 2617]
50. Existing and future therapeutic options for hepatitis C virus infection.
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