26 results on '"Cuzzucoli Crucitti, Giuliana"'
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2. Discovery of N-aryl-naphthylamines as in vitro inhibitors of the interaction between HIV integrase and the cofactor LEDGF/p75
3. Pyrrolyl-Hydroxamates for use in the prevention and/or treatment of bacterial infections
4. Diaryl Disulfides as Novel Stabilizers of Tumor Suppressor Pdcd4
5. New Nucleotide-Competitive Non-Nucleoside Inhibitors of Terminal 2 Deoxynucleotidyl Transferase: Discovery, Characterization, and 3 Crystal Structure in Complex with the Target
6. PIRROLIL-IDROSSAMMATI PER USO NELLA PREVENZIONE E/O NEL TRATTAMENTO DI INFEZIONI BATTERICHE
7. Heterocyclic compounds endowed with antiviral activity
8. N-Substituted Quinolinonyl Diketo Acid Derivatives as HIV Integrase Strand Transfer Inhibitors and Their Activity against RNase H Function of Reverse Transcriptase
9. Structure–Activity Relationship of Pyrrolyl Diketo Acid Derivatives as Dual Inhibitors of HIV-1 Integrase and Reverse Transcriptase Ribonuclease H Domain
10. The first potent diphenyl phosphonate KLK4 inhibitors with unexpected binding kinetics
11. Identification of Highly Conserved Residues Involved in Inhibition of HIV-1 RNase H Function by Diketo Acid Derivatives
12. Basic Quinolinonyl Diketo Acid Derivatives as Inhibitors of HIV Integrase and their Activity against RNase H Function of Reverse Transcriptase
13. 6-(1-Benzyl-1H-pyrrol-2-yl)-2,4-dioxo-5-hexenoic Acids as Dual Inhibitors of Recombinant HIV-1 Integrase and Ribonuclease H, Synthesized by a Parallel Synthesis Approach
14. New Nucleotide-Competitive Non-Nucleoside Inhibitors of Terminal Deoxynucleotidyl Transferase: Discovery, Characterization, and Crystal Structure in Complex with the Target
15. ChemInform Abstract: Convenient Route to 2H-Pyrrolo [3,4-b]Quinolin-9(4H)-one Skeleton via TosMIC Reaction.
16. Discovery and Pharmacological Profile of New 1H-Indazole-3-carboxamide and 2H-Pyrrolo[3,4-c]quinoline Derivatives as Selective Serotonin 4 Receptor Ligands
17. Design, Synthesis, and Structure–Activity Relationship ofN-Arylnaphthylamine Derivatives as Amyloid Aggregation Inhibitors
18. Structure–ActivityRelationship of PyrrolylDiketo Acid Derivatives as Dual Inhibitors of HIV-1 Integraseand Reverse Transcriptase Ribonuclease H Domain.
19. Basic Quinolinonyl DiketoAcid Derivatives as Inhibitorsof HIV Integrase andtheir Activity against RNase H Function of Reverse Transcriptase.
20. 6-(1-Benzyl-1H-pyrrol-2-yl)-2,4-dioxo-5-hexenoicAcids as Dual Inhibitors of Recombinant HIV-1 Integrase andRibonuclease H, Synthesized by a Parallel Synthesis Approach.
21. New Nucleotide-CompetitiveNon-Nucleoside Inhibitors of Terminal Deoxynucleotidyl Transferase:Discovery, Characterization, and Crystal Structure in Complex withthe Target.
22. Discovery and PharmacologicalProfile of New 1H-Indazole-3-carboxamide and2H-Pyrrolo[3,4-c]quinolineDerivatives as Selective Serotonin 4 ReceptorLigands.
23. Design, Synthesis, andStructure–Activity Relationship of N-ArylnaphthylamineDerivatives as Amyloid Aggregation Inhibitors.
24. Discovery of N-aryl-naphthylamines as in vitro inhibitors of the interaction between HIV integrase and the cofactor LEDGF/p75
25. N‑substituted quinolinonyl diketo acid derivatives as HIV integrase strand transfer inhibitors and their activity against RNase H function of reverse transcriptase
26. Design, synthesis, and structure-activity relationship of N-arylnaphthylamine derivatives as amyloid aggregation inhibitors.
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