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2. Potent Long-Acting Inhibitors Targeting the HIV-1 Capsid Based on a Versatile Quinazolin-4-one Scaffold

3. Scaffold modifications to the 4-(4,4-dimethylpiperidinyl) 2,6-dimethylpyridinyl class of HIV-1 allosteric integrase inhibitors

4. Discovery and Preclinical Profiling of GSK3839919, a Potent HIV-1 Allosteric Integrase Inhibitor

10. Development of the Large-Scale Synthesis of Tetrahydropyran Glycine, a Precursor to the HCV NS5A Inhibitor BMS-986097

11. Synergistic Activity of Combined NS5A Inhibitors

12. Resensitizing daclatasvir-resistant hepatitis C variants by allosteric modulation of NS5A

14. Hepatitis C Virus NS5A Replication Complex Inhibitors: The Discovery of Daclatasvir

15. Discovery and Development of Hepatitis C Virus NS5A Replication Complex Inhibitors

16. Hepatitis C Virus NS5A Replication Complex Inhibitors. Part 6: Discovery of a Novel and Highly Potent Biarylimidazole Chemotype with Inhibitory Activity Toward Genotypes 1a and 1b Replicons

18. Characterizations of HCV NS5A replication complex inhibitors

19. HCV NS5A replication complex inhibitors. Part 5: Discovery of potent and pan-genotypic glycinamide cap derivatives

20. HCV NS5A Replication Complex Inhibitors. Part 4.1 Optimization for Genotype 1a Replicon Inhibitory Activity

21. Antiviral Drug Discovery

22. HCV NS5A replication complex inhibitors. Part 3: discovery of potent analogs with distinct core topologies

23. HCV NS5A replication complex inhibitors. Part 2: Investigation of stilbene prolinamides

24. The effects of NS5A inhibitors on NS5A phosphorylation, polyprotein processing and localization

25. Chemical genetics strategy identifies an HCV NS5A inhibitor with a potent clinical effect

26. Synthesis and structure–activity relationship of imidazo(1,2-a)thieno(3,2-e)pyrazines as IKK-β inhibitors

27. Synthesis and biological evaluation of 4-amino derivatives of benzimidazoquinoxaline, benzimidazoquinoline, and benzopyrazoloquinazoline as potent IKK inhibitors

28. Developments in Antiviral Drug Design, Discovery and Development in 2004

32. Triethyl Orthoacetate

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