145 results on '"Meleddu, Rita"'
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2. Privileged Scaffold Hybridization in the Design of Carbonic Anhydrase Inhibitors.
3. Suppression of lipopolysaccharide-induced COX-2 expression via p38MAPK, JNK, and C/EBPβ phosphorylation inhibition by furomagydarin A, a benzofuran glycoside from Magydaris pastinacea
4. 2H-chromene and 7H-furo-chromene derivatives selectively inhibit tumour associated human carbonic anhydrase IX and XII isoforms
5. 5-Nitro-3-(2-(4-phenylthiazol-2-yl)hydrazineylidene)indolin-2-one derivatives inhibit HIV-1 replication by a multitarget mechanism of action
6. Natural product-inspired esters and amides of ferulic and caffeic acid as dual inhibitors of HIV-1 reverse transcriptase
7. Drug design, synthesis, in vitro and in silico evaluation of selective monoaminoxidase B inhibitors based on 3-acetyl-2-dichlorophenyl-5-aryl-2,3-dihydro-1,3,4-oxadiazole chemical scaffold
8. (3Z)-3-(2-[4-(aryl)-1,3-thiazol-2-yl]hydrazin-1-ylidene)-2,3-dihydro-1H-indol-2-one derivatives as dual inhibitors of HIV-1 reverse transcriptase
9. Synthesis and biological assessment of novel 2-thiazolylhydrazones and computational analysis of their recognition by monoamine oxidase B
10. 2-Acylhydrazino-5-arylpyrrole derivatives: Synthesis and antifungal activity evaluation
11. Synthesis, biological evaluation, and SAR study of novel pyrazole analogues as inhibitors of Mycobacterium tuberculosis: Part 2. Synthesis of rigid pyrazolones
12. Exploring New Scaffolds for the Dual Inhibition of HIV-1 RT Polymerase and Ribonuclease Associated Functions
13. Synthesis, biological evaluation and SAR study of novel pyrazole analogues as inhibitors of Mycobacterium tuberculosis
14. Flavonoids and Acid-Hydrolysis derivatives of Neo-Clerodane diterpenes from Teucrium flavum subsp. glaucum as inhibitors of the HIV-1 reverse transcriptase–associated RNase H function
15. Selective inhibition of carbonic anhydrase IX and XII by coumarin and psoralen derivatives
16. New Dihydrothiazole Benzensulfonamides: Looking for Selectivity toward Carbonic Anhydrase Isoforms I, II, IX, and XII
17. Coumarins fromMagydaris pastinaceaas inhibitors of the tumour-associated carbonic anhydrases IX and XII: isolation, biological studies and in silico evaluation
18. Ferulic Acid Esters and Withanolides: In Search of Withania somnifera GABAA Receptor Modulators
19. Exploring new structural features of the 4-[(3-methyl-4-aryl-2,3-dihydro-1,3-thiazol-2-ylidene)amino]benzenesulphonamide scaffold for the inhibition of human carbonic anhydrases
20. Investigating the Anticancer Activity of Isatin/Dihydropyrazole Hybrids
21. Coumarins from Magydaris pastinacea as inhibitors of the tumour-associated carbonic anhydrases IX and XII: isolation, biological studies and in silico evaluation.
22. Tuning the Dual Inhibition of Carbonic Anhydrase and Cyclooxygenase by Dihydrothiazole Benzensulfonamides
23. Targeting Tumor Associated Carbonic Anhydrases IX and XII: Highly Isozyme Selective Coumarin and Psoralen Inhibitors
24. Through scaffold modification to 3,5-diaryl-4,5-dihydroisoxazoles: new potent and selective inhibitors of monoamine oxidase B
25. New 4-[(3-cyclohexyl-4-aryl-2,3-dihydro-1,3-thiazol-2-ylidene)amino]benzene-1-sulfonamides, synthesis and inhibitory activity toward carbonic anhydrase I, II, IX, XII
26. Phenylpropenoids from Bupleurum fruticosum as Anti-Human Rhinovirus Species A Selective Capsid Binders
27. N-Acylbenzenesulfonamide Dihydro-1,3,4-oxadiazole Hybrids: Seeking Selectivity toward Carbonic Anhydrase Isoforms
28. Through scaffold modification to 3,5-diaryl-4,5-dihydroisoxazoles: new potent and selective inhibitors of monoamine oxidase B
29. Ferulic Acid Esters and Withanolides: In Search of Withania somnifera GABAA Receptor Modulators.
30. Investigating the Anticancer Activity of Isatin/Dihydropyrazole Hybrids.
31. Ferulic Acid Esters and Withanolides: In Search of Withania somniferaGABAAReceptor Modulators
32. Isatin: a privileged scaffold for the design of carbonic anhydrase inhibitors
33. Isatin thiazoline hybrids as dual inhibitors of HIV-1 reverse transcriptase
34. Ribonuclease H/DNA Polymerase HIV-1 Reverse Transcriptase Dual Inhibitor: Mechanistic Studies on the Allosteric Mode of Action of Isatin-Based Compound RMNC6
35. Exploring the thiazole scaffold for the identification of new agents for the treatment of fluconazole resistant Candida
36. Synthesis of different series of small molecules targeting HIV-1 RT, Candida albicans, MAO and G-Quadruplex
37. Isatin: a privileged scaffold for the design of carbonic anhydrase inhibitors.
38. Isatin thiazoline hybrids as dual inhibitors of HIV-1 reverse transcriptase.
39. Design, Synthesis, and Biological Evaluation of 1,3-Diarylpropenones as Dual Inhibitors of HIV-1 Reverse Transcriptase
40. 1,5-Diaryl-2-ethyl pyrrole derivatives as antimycobacterial agents: Design, synthesis, and microbiological evaluation
41. Synthesis and biological evaluation of new enantiomerically pure azole derivatives as inhibitors of Mycobacterium tuberculosis
42. Site directed mutagenesis studies on HIV-1 reverse transcriptase (RT) shed light on the mechanism of action of a new Ribonuclease H/ DNA polymerase RT dual inhibitor
43. A Novel Series of 3,4‐Disubstituted Dihydropyrazoles: Synthesis and Evaluation for MAO Enzyme Inhibition
44. Molecular Aspects of the RT/drug Interactions. Perspective of Dual Inhibitors
45. Phenylpropenoids from Bupleurum fruticosumas Anti-Human Rhinovirus Species A Selective Capsid Binders
46. 3-Acetyl-2,5-diaryl-2,3-dihydro-1,3,4-oxadiazoles: A New Scaffold for the Selective Inhibition of Monoamine Oxidase B
47. Semicarbazide-sensitive amine oxidase/vascular adhesion protein-1: a patent survey
48. Design and Synthesis of New Isatin Derivatives as HIV-1 Reverse Transcriptase Associated Ribonuclease H Inhibitors
49. ChemInform Abstract: Synthesis and Biological Evaluation of New Enantiomerically Pure Azole Derivatives as Inhibitors of Mycobacterium tuberculosis.
50. Novel N-aryl- and N-heteryl phenazine-1-carboxamides as potential agents for the treatment of infections sustained by drug-resistant and multidrug-resistant Mycobacterium tuberculosis
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