21 results on '"Chudinov, Mikhail"'
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2. Scaffold hopping in the oxadiazole antibiotic structure leads to more active compounds
3. Molecular Periphery Design Allows Control of the New Nitrofurans Antimicrobial Selectivity.
4. The Nitrofuran-Warhead-Equipped Spirocyclic Azetidines Show Excellent Activity against Mycobacterium tuberculosis.
5. Parallel synthesis of derivatives of 1H-1,2,4-triazole-3-carboxylic acids with heterocyclic substituents at position 5
6. 5-Nitrofuran-Tagged Oxazolyl Pyrazolopiperidines: Synthesis and Activity against ESKAPE Pathogens
7. Novel 5-alkyl(aryl)-substituted ribavirine analogues: synthesis and antiviral evaluation
8. Chemo-enzymatic synthesis of 5-substituted ribavirin analogs: Unexpected cooperative effect in the interaction of 5-alkyloxymethyl 1,2,4-triazol-3-carboxamides with E. coli purine nucleoside phosphorylase active site
9. Exploration of Spirocyclic Derivatives of Ciprofloxacin as Antibacterial Agents
10. Chemo-Enzymatic Synthesis of 5-Substituted Ribavirin Analogs: Unexpected Cooperative Effect in the Interaction of 5-Alkyloxymethyl 1,2,4-Triazol-3-Carboxamides with E. Coli Purine Nucleoside Phosphorylase Active Site
11. 5‐Substituted 1,2,4‐Triazole‐3‐Carboxylates and 5‐Substituted Ribavirin Analogs Synthesis
12. Progress in the medicinal chemistry of organoboron compounds
13. Strained contacts with the cell membrane may influence ligand affinity to G protein coupled receptors: a case of free fatty acid receptor 1 agonists
14. Nucleoside Analogs with Fleximer Nucleobase
15. 5-Nitrofuran-2-yl Thiohydrazones as Double Antibacterial Agents Synthesis and In Vitro Evaluation
16. 5-alkylvinyl-1,2,4-triazole nucleosides: Synthesis and biological evaluation
17. Isosteric ribavirin analogues: Synthesis and antiviral activities
18. Chemical ribosylation of 5-substituted 1,2,4-triazole-3-carboxylates
19. An alternative route to the arylvinyltriazole nucleosides
20. Optimization of Antiviral Prodrug Properties Using Combinatorial Methods
21. Optimization of Antiviral Prodrug Properties Using Combinatorial Methods
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