228 results on '"Balzarini Jan"'
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2. Crucial role of the N-glycans on the viral E-envelope glycoprotein in DC-SIGN-mediated dengue virus infection
3. Synthesis and biological evaluation of pyrimidine nucleoside monophosphate prodrugs targeted against influenza virus
4. Selective inhibition of Human Immunodeficiency Virus type 1 (HIV-1) by a novel family of tricyclic nucleosides
5. The rare HIV-1 gp41 mutations 43T and 50V elevate enfuvirtide resistance levels of common enfuvirtide resistance mutations that did not impact susceptibility to sifuvirtide
6. Conservation of antiviral activity and improved selectivity in PMEO-DAPym upon pyrimidine to triazine scaffold hopping
7. Capture and transmission of HIV-1 by the C-type lectin L-SIGN (DC-SIGNR) is inhibited by carbohydrate-binding agents and polyanions
8. Efficient conversion of tetrapeptide-based TSAO prodrugs to the parent drug by dipeptidyl-peptidase IV (DPPIV/CD26)
9. Plant lectins are potent inhibitors of coronaviruses by interfering with two targets in the viral replication cycle
10. Inhibition of feline (FIPV) and human (SARS) coronavirus by semisynthetic derivatives of glycopeptide antibiotics
11. Therapeutic strategies towards HIV-1 infection in macrophages
12. Aryl furano pyrimidines: The most potent and selective anti-VZV agents reported to date
13. Discovery of TSAO derivatives with an unusual HIV-1 activity/resistance profile
14. Synergistic in vitro anti-HIV type 1 activity of tenofovir with carbohydrate-binding agents (CBAs)
15. Identification of a N-linked Glycan on HIV-1 gp120 that is Indispensable for Viral Entry: 20
16. Novel 9-Arylpurines, as Selective Inhibitors of In Vitro Enterovirus Replication: 180
17. Design, Synthesis and Evaluation of Novel Anti-VZV BCNAs: 33
18. Enzyme-triggered CycloSal-Pronucleotides: 27
19. Chemical Stability and Intracellular Metabolism of 1-(S)-[3-Hydroxy-2-(Phosphonomethoxy)Propyl]-5-Azacytosine: 145
20. Properties of Aminoacid Esters Linked to Cyclo Sal-Pronucleotides: 110
21. Design, Synthesis, and Biological Evaluation of Novel Anti-VZV Agents: 108
22. Design and Synthesis of Novel Anti-HCMV Agents: Modifications to the Bicyclic Pyrimidine Base: 106
23. In Vivo Antiviral Activity of 1-(S)-[3-Hydroxy-2-(Phosphonomethoxy)Propyl]-5-Azacytosine and its Cyclic Form: 17
24. Synthesis and Antiviral Activity of 1-(S)-[3-Hydroxy-2-(Phosphonomethoxy)Propyl]-5-Azacytosine and its Ester Prodrugs: 16
25. Introduction to the Special Issue dedicated to Prof. Erik De Clercq for reaching the Professor Emeritus status at the Katholieke Universiteit Leuven
26. HIV-1 Strains Resistant to Mannose- and N-Acetylglucosamine-Binding Proteins Show Mutations at Glycosylation Sites of gp120: 33
27. The Predominant Mechanism by which Ribavirin Exerts its Antiviral Activity In Vitro Against Flaviviruses and Paramyxoviruses is Mediated by Inhibition of Inosine Monophosphate Dehydrogenase: 27
28. Novel "Lock-In" Modified cycloSal Nucleotides (II): Application of the AM- and the POM-Group: 1
29. N-Aminoimidazole Derivatives Inhibit HIV-1 Gene Expression by an Unexploited Mechanism of Action: 39
30. Pre-Clinical Development of the BCNAs: The Most Potent Anti-VZV Agents Reported to Date: 14
31. Chemotherapy of Human Immunodeficiency Virus by Pradimicin A: A Novel Therapeutic Concept for Treatment of Glycosylated Enveloped Viruses: 6
32. Stereoselective Synthesis and Biological Evaluation of d- and L-carba-Nucleosides as Potential Antiviral Agents: 4
33. HIV-1 Strains Resistant to Mannose- and N-Acetylglucosamine-Binding Proteins Show Mutations at Glycosylation Sites of gp120: 33
34. The Predominant Mechanism by which Ribavirin Exerts its Antiviral Activity In Vitro Against Flaviviruses and Paramyxoviruses is Mediated by Inhibition of Inosine Monophosphate Dehydrogenase: 27
35. Novel "Lock-In" Modified cycloSal Nucleotides (II): Application of the AM- and the POM-Group: 1
36. Synthesis and antiviral evaluation of some β- l-2′,3′-dideoxy-5-chloropyrimidine nucleosides and pronucleotides
37. Indolylarylsulfones as HIV-1 Non-Nucleoside Reverse Transcriptase Inhibitors: New Cyclic Substituents at the Indole-2-carboxamide
38. A Novel Family of Multivalent Compounds able to Interact with GP120: Anti-HIV Evaluation and Binding Analysis With Surface Plasmon Resonance
39. Tripartate Prodrugs of Hydroxy-containing Compounds
40. Synthesis and Antiviral Evaluation of N9-[2-(Phosphonomethoxy)ethyl] (PME) Analogues Derived from 8-Substituted Purines
41. Antiviral Activity of Acyclic Nucleoside Phosphonates with Branched 2-(2-Phosphonoethoxy)ethyl Chain
42. First Diastereoselective Synthesis of Pronucleotides
43. Lectins and T-20, but not Neutralizing Antibodies, Inhibit HIV-1 Env-mediated Syncytium Formation between Clone69t1RevEnv and Supt1 Cells Monitored by Fluorescence Microscopy
44. Inhibition of Hepatitis C Virus Replication by Semisynthetic Derivatives of Glycopeptide Antibiotics
45. Synthesis and Antiviral Evaluation of 3-(2,3-Dihydroxypropyl)furo[2,3-d]pyrimidin-2(3H)-ones
46. Lipophilic Nucleoside Diphosphate Prodrugs—Synthesis and Properties
47. A Chemoenzymatic Synthesis of Carbocyclic Nucleosides and Nucleotides
48. Stereoselective Synthetic Strategy to Potentially Antiviral Active Carbocyclic l-Nucleosides and l-Nucleotides
49. Synthesis of Ester Prodrugs of 9-(S)-[3-Hydroxy-2-(phosphonomethoxy)propyl]-2,6-diaminopurine (HPMPDAP) as Anti-Poxvirus Agents
50. Stereoselective Synthesis of Different Types of Nucleotide Prodrugs
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