49 results on '"Parhi, Ajit"'
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2. Combination with a FtsZ inhibitor potentiates the in vivo efficacy of oxacillin against methicillin-resistant Staphylococcus aureus
3. Evaluation of 2,6-difluoro-3-(oxazol-2-ylmethoxy)benzamide chemotypes as Gram-negative FtsZ inhibitors
4. Structure-activity relationships of potentiators of the antibiotic activity of clarithromycin against Escherichia coli
5. Advances in the structural studies of antibiotic potentiators against Escherichia coli
6. Inhibition of RND-type efflux pumps confers the FtsZ-directed prodrug TXY436 with activity against Gram-negative bacteria
7. Pharmacokinetics and in vivo antistaphylococcal efficacy of TXY541, a 1-methylpiperidine-4-carboxamide prodrug of PC190723
8. Phenyl substituted 3-hydroxypyridin-2(1H)-ones: Inhibitors of influenza A endonuclease
9. Enterococcal and streptococcal resistance to PC190723 and related compounds: Molecular insights from a FtsZ mutational analysis
10. Antimicrobial activity of various 4- and 5-substituted 1-phenylnaphthalenes
11. 3-Phenyl substituted 6,7-dimethoxyisoquinoline derivatives as FtsZ-targeting antibacterial agents
12. Evaluation of A22 Analogs as Gram-negative Antimicrobial Agents
13. Novel MreB Inhibitors with Antibacterial Activity Against Gram (-) Bacteria
14. Evaluation of a Conformationally Constrained Indole Carboxamide as a Potential Efflux Pump Inhibitor in Pseudomonas aeruginosa
15. TXH11106: A Third-Generation MreB Inhibitor with Enhanced Activity against a Broad Range of Gram-Negative Bacterial Pathogens
16. In vivo studies of the SERT-selective [ 18F]FPBM and VMAT2-selective [ 18F]AV-133 radiotracers in a rat model of Parkinson's disease
17. Evaluation of Heterocyclic Carboxamides as Potential Efflux Pump Inhibitors in Pseudomonas aeruginosa
18. 2-(2′-((Dimethylamino)methyl)-4′-(3-[ 18F]fluoropropoxy)-phenylthio)benzenamine for positron emission tomography imaging of serotonin transporters
19. Synthesis of the mixed acetal segment of S-glyceroplasmalopsychosine
20. TXA497 as a topical antibacterial agent: Comparative antistaphylococcal, skin deposition, and skin permeation studies with mupirocin
21. Medium effects on the reactions of coordination complexes: Base hydrolysisof(αβS)(p-hydroxybenzoato)(tetraethylenepentamine) cobalt(III) in iso-propanol–water, tert-butanol–water and dimethyl sulfoxide–water media
22. The Ramberg-Bäcklund Way to C-Glycosides
23. Medium effect on the reactions of complexes: kinetics and mechanism of the base hydrolysis of cis-[(salicylato)(amine)bis(ethylenediamine)cobalt(III)] compounds in methanol-water
24. β-Lactam Antibiotics with a High Affinity for PBP2 Act Synergistically with the FtsZ-Targeting Agent TXA707 against Methicillin-Resistant Staphylococcus aureus
25. Structural Flexibility of an Inhibitor Overcomes Drug Resistance Mutations in Staphylococcus aureus FtsZ
26. Antibacterial activity of quinoxalines, quinazolines, and 1,5-naphthyridines
27. Substituted 1,6-diphenylnaphthalenes as FtsZ-targeting antibacterial agents
28. Combining the FtsZ-Targeting Prodrug TXA709 and the Cephalosporin Cefdinir Confers Synergy and Reduces the Frequency of Resistance in Methicillin-Resistant Staphylococcus aureus
29. Antibacterial activity of substituted 5-methylbenzo[c]phenanthridinium derivatives
30. Antibacterial activity of substituted dibenzo[a,g]quinolizin-7-ium derivatives
31. In Vivo Pharmacodynamic Evaluation of an FtsZ Inhibitor, TXA-709, and Its Active Metabolite, TXA-707, in a Murine Neutropenic Thigh Infection Model
32. TXA709, an FtsZ-Targeting Benzamide Prodrug with Improved Pharmacokinetics and Enhanced In Vivo Efficacy against Methicillin-Resistant Staphylococcus aureus
33. Comparison of the SERT-selective [18F]FPBM and VMAT2-selective [18F]AV-133 radiotracers in a rat model of Parkinson’s Disease
34. An FtsZ-Targeting Prodrug with Oral Antistaphylococcal Efficacy In Vivo
35. Crystallographic Fragment Screening and Structure-Based Optimization Yields a New Class of Influenza Endonuclease Inhibitors
36. 3-Hydroxyquinolin-2(1H)-ones As Inhibitors of Influenza A Endonuclease
37. Synthesis of fluorescent probes based on stilbenes and diphenylacetylenes targeting β-amyloid plaques
38. A Bactericidal Guanidinomethyl Biaryl That Alters the Dynamics of Bacterial FtsZ Polymerization
39. In Vivo Characterization of a Series of 18F-Diaryl Sulfides (18F-2-(2′-((Dimethylamino)Methyl)-4′-(Fluoroalkoxy)Phenylthio)Benzenamine) for PET Imaging of the Serotonin Transporter
40. 2-(2′-((Dimethylamino)methyl)-4′-(fluoroalkoxy)-phenylthio)benzenamine Derivatives as Serotonin Transporter Imaging Agents
41. The Ramberg—Baecklund Way to C‐Glycosides
42. A Weinreb Nitrile Oxide and Nitrone for Cycloaddition.
43. In VivoPharmacodynamic Evaluation of an FtsZ Inhibitor, TXA-709, and Its Active Metabolite, TXA-707, in a Murine Neutropenic Thigh Infection Model
44. TXA709, an FtsZ-Targeting Benzamide Prodrug with Improved Pharmacokinetics and Enhanced In VivoEfficacy against Methicillin-Resistant Staphylococcus aureus
45. A Bactericidal GuanidinomethylBiaryl That Altersthe Dynamics of Bacterial FtsZ Polymerization.
46. In Vivo Characterization of a Series of 18F-Diaryl Sulfides (18F-2-(2'-((Dimethylamino)Methyl)-49-(Fluoroalkoxy) Phenylthio)Benzenamine) for PET Imaging of the Serotonin Transporter.
47. Evaluation of Heterocyclic Carboxamides as Potential Efflux Pump Inhibitors in Pseudomonas aeruginosa.
48. Medium effect on the reactions of complexes: kinetics and mechanism of the base hydrolysis of cis-[(salicylato)(amine) bis(ethylenediamine)cobalt(III)] compounds in methanol-water.
49. A Weinreb nitrile oxide and nitrone for cycloaddition.
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