17 results on '"Golub, Andriy G."'
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2. Discovery of potent anti-tuberculosis agents targeting leucyl-tRNA synthetase
3. Identification of apoptosis signal-regulating kinase 1 (ASK1) inhibitors among the derivatives of benzothiazol-2-yl-3-hydroxy-5-phenyl-1,5-dihydro-pyrrol-2-one
4. Discovery and characterization of synthetic 4′-hydroxyflavones—New CK2 inhibitors from flavone family
5. Rational design of apoptosis signal-regulating kinase 1 inhibitors: Discovering novel structural scaffold
6. Synthesis and biological evaluation of substituted (thieno[2,3-d]pyrimidin-4-ylthio)carboxylic acids as inhibitors of human protein kinase CK2
7. Structure-based discovery of novel flavonol inhibitors of human protein kinase CK2
8. ASK1 pharmacophore model derived from diverse classes of inhibitors
9. Identification of novel PARP-1 inhibitors by structure-based virtual screening
10. Identification of Mycobacterium tuberculosis leucyl-tRNA synthetase (LeuRS) inhibitors among the derivatives of 5-phenylamino-2H-[1,2,4]triazin-3-one
11. Discovery of new scaffolds for rational design of HCV NS5B polymerase inhibitors
12. A Note of Caution on the Role of Halogen Bonds for Protein Kinase/Inhibitor Recognition Suggested by High- And Low-Salt CK2α Complex Structures
13. Structural Hypervariability of the Two Human Protein Kinase CK2 Catalytic Subunit Paralogs Revealed by Complex Structures with a Flavonoland a Thieno[2,3-d]pyrimidine-Based Inhibitor.
14. In vitro Activation of heme oxygenase-2 by menadione and its analogs
15. Identification of 3H-Naphtho[1,2,3-de]quinoline-2,7-diones as Inhibitors of Apoptosis Signal-Regulating Kinase 1 (ASK1)
16. Evaluation of 3-Carboxy-4(1H)-quinolones as Inhibitors of Human Protein Kinase CK2
17. Structural Hypervariability of the Two Human Protein Kinase CK2 Catalytic Subunit Paralogs Revealed by Complex Structures with a Flavonol- and a Thieno[2,3-d]pyrimidine-Based Inhibitor.
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