166 results on '"Riabova, Olga"'
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2. The novel drug candidate VOMG kills Mycobacterium abscessus and other pathogens by inhibiting cell division
3. Molecular mechanism of rhinovirus escape from the Pyrazolo[3,4-d]pyrimidine capsid-binding inhibitor OBR-5-340 via mutations distant from the binding pocket: Derivatives that brake resistance
4. Benzothiozinone derivatives with anti-tubercular Activity−Further side chain investigation
5. Efficacy of macozinone in mice with genetically diverse susceptibility to Mycobacterium tuberculosis infection
6. Efficacy of an isoxazole-3-carboxamide analog of pleconaril in mouse models of Enterovirus-D68 and Coxsackie B5
7. Multiple approaches to repurposing drugs for neuroblastoma
8. SCRAPPY - a single cell rapid assay of proteome perturbation in yeast uncovers a joint role of aromatic amino acids and oxidative stress in the toxicity of lipophilic nucleoside analogs
9. Characterization of the dispirotripiperazine derivative PDSTP as antibiotic adjuvant and antivirulence compound against Pseudomonas aeruginosa
10. Determination of alkaloid-inspired molecule vindeburnol in rabbit plasma by UPLC–HRMS and its application to pharmacokinetic studies and preliminary metabolite identification
11. 1-Sulfonyl-3-amino-1H-1,2,4-triazoles as Yellow Fever Virus Inhibitors: Synthesis and Structure–Activity Relationship
12. Benzothiozinone derivatives with anti-tubercular Activity−Further side chain investigation
13. Antiviral Evaluation of Dispirotripiperazines against Hepatitis B Virus
14. Side Chain-Modified Benzothiazinone Derivatives with Anti-Mycobacterial Activity
15. Antidepressant-like Effect of the Eburnamine-Type Molecule Vindeburnol in Rat and Mouse Models of Ultrasound-Induced Depression.
16. Side Chain-modified Benzothiazinone Derivatives with Anti-Mycobacterial Activity
17. N-Phenyl-1-(phenylsulfonyl)-1H-1,2,4-triazol-3-amine as a New Class of HIV-1 Non-nucleoside Reverse Transcriptase Inhibitor
18. Antituberculosis Macozinone Extended-Release Tablets To Enhance Bioavailability: a Pilot Pharmacokinetic Study in Beagle Dogs
19. Thieno[2,3‐ d ]pyrimidine‐Core Compounds Show Activity against Clinically Relevant Gram‐Positive Bacteria
20. A proof-of-concept study for the efficacy of dispirotripiperazine PDSTP in a rabbit model of herpes simplex epithelial keratitis
21. Pyronaridine Protects against SARS-CoV-2 Infection in Mouse
22. Machine Learning Models for Mycobacterium tuberculosis In Vitro Activity: Prediction and Target Visualization
23. Strain dependent structural effects and in vivo efficacy of enterovirus-D68 inhibitors
24. Pyronaridine Protects Against SARS-CoV-2 in Mouse
25. Exposure to nitric oxide drives transition to resuscitation-promoting factor-dependency in mycobacteria
26. Discovery of new diketopiperazines inhibiting Burkholderia cenocepacia quorum sensing in vitro and in vivo
27. Molecular mechanism of a specific capsid binder resistance caused by mutations outside the binding pocket
28. New pleconaril and [(biphenyloxy)propyl]isoxazole derivatives with substitutions in the central ring exhibit antiviral activity against pleconaril-resistant coxsackievirus B3
29. Thieno[2,3‐d]pyrimidine‐Core Compounds Show Activity against Clinically Relevant Gram‐Positive Bacteria.
30. Development of Machine Learning Models and the Discovery of a New Antiviral Compound against Yellow Fever Virus
31. Discovery of 5-Nitro-6-thiocyanatopyrimidines as Inhibitors of Cryptococcus neoformans and Cryptococcus gattii
32. QSAR analysis of [(biphenyloxy)propyl]isoxazoles: agents against coxsackievirus B3
33. 6,11-Dioxobenzo[f]pyrido[1,2-a]indoles Kill Mycobacterium tuberculosis by Targeting Iron–Sulfur Protein Rv0338c (IspQ), A Putative Redox Sensor
34. The past, present and future of RNA respiratory viruses: influenza and coronaviruses
35. Chemical, Metabolic, and Cellular Characterization of a FtsZ Inhibitor Effective Against Burkholderia cenocepacia
36. Rv0579 Is Involved in the Resistance to the TP053 Antitubercular Prodrug
37. Per aspera ad astra: application of Simplex QSAR approach in antiviral research
38. Machine Learning Models for Mycobacterium tuberculosis In Vitro Activity: Prediction and Target Visualization.
39. Influence of Substitutes in the Central Phenyl Ring of Capsid Function Inhibitors on Anti-coxsackievirus B3 Activity: 146
40. Synthesis and antileprosy activity of some dialkyldithiocarbamates
41. Susceptibility of coxsackievirus B3 laboratory strains and clinical isolates to the capsid function inhibitor pleconaril: antiviral studies with virus chimeras demonstrate the crucial role of amino acid 1092 in treatment
42. Novel [(biphenyloxy)propyl]isoxazole derivatives for inhibition of human rhinovirus 2 and coxsackievirus B3 replication
43. New Insights into the Mechanism of Action of the Thienopyrimidine Antitubercular Prodrug TP053
44. Machine Learning Models for Mycobacterium tuberculosisIn VitroActivity: Prediction and Target Visualization
45. Competitive Fitness of Essential Gene Knockdowns Reveals a Broad-Spectrum Antibacterial Inhibitor of the Cell Division Protein FtsZ
46. MOESM1 of Benzoylphenyl thiocyanates are new, effective inhibitors of the mycobacterial resuscitation promoting factor B protein
47. Structure-Based Drug Design and Characterization of Sulfonyl-Piperazine Benzothiazinone Inhibitors of DprE1 from Mycobacterium tuberculosis
48. The Thienopyrimidine TP053 Prodrug Kills Mycobacterium Tuberculosis Cells by Nitric Oxide Release
49. Copper-related toxicity in replicating and dormantMycobacterium tuberculosiscaused by 1-hydroxy-5-R-pyridine-2(1H)-thiones
50. Benzoylphenyl thiocyanates are new, effective inhibitors of the mycobacterial resuscitation promoting factor B protein
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