213 results on '"Yarovaya, Olga I."'
Search Results
2. Global LC-MS/MS targeted metabolomics using a combination of HILIC and RP LC separation modes on an organic monolithic column based on 1-vinyl-1,2,4-triazole
3. Development of an LC-MS/MS-based method for quantification and pharmacokinetics study on SCID mice of a dehydroabietylamine-adamantylamine conjugate, a promising inhibitor of the DNA repair enzyme
4. Synthesis and antiviral properties of tricyclic amides derived from α-humulene and β-caryophyllene
5. 1,3-Dipolar Cycloaddition of Nitrile Oxides and Nitrilimines to (−)-β-Caryophyllene: Stereoselective Synthesis of Polycyclic Derivatives and Their Biological Testing.
6. 2-Aryl-1-hydroxyimidazoles possessing antiviral activity against a wide range of orthopoxviruses, including the variola virus.
7. Nitrogen-Containing Heterocyclic Compounds Obtained from Monoterpenes or Their Derivatives: Synthesis and Properties
8. Biostability study, quantitation method and preliminary pharmacokinetics of a new antifilovirus agent based on borneol and 3-(piperidin-1-yl)propanoic acid
9. Quaternary ammonium salts based on (-)-borneol as effective inhibitors of influenza virus
10. Monoterpenoid-based inhibitors of filoviruses targeting the glycoprotein-mediated entry process
11. Synthesis and antiviral activity of novel 3-substituted pyrazolinium salts
12. Synthesis and Antiviral Activity of N-Heterocyclic Hydrazine Derivatives of Camphor and Fenchone
13. Halosulfonamidation of camphene: chemo and stereoselectivity, rearrangement, solvent interception, heterocyclization.
14. Development and validation of an LC-MS/MS method for the quantitative analysis of the anti-influenza agent camphecene in rat plasma and its application to study the blood-to-plasma distribution of the agent
15. The Potential of Usnic-Acid-Based Thiazolo-Thiophenes as Inhibitors of the Main Protease of SARS-CoV-2 Viruses
16. Single-stage synthesis of heterocyclic alkaloid-like compounds from (+)-camphoric acid and their antiviral activity
17. Design, synthesis and antiviral evaluation of novel conjugates of the 1,7,7‐trimethylbicyclo[2.2.1]heptane scaffold and saturated N‐heterocycles via 1,2,3‐triazole linker.
18. Synthesis of Norabietyl and Nordehydroabietyl Imidazolidine-2,4,5-Triones and Their Activity against Tyrosyl-DNA Phosphodiesterase 1
19. Corrigendum: The main protease 3CLpro of the SARS-CoV-2 virus: how to turn an enemy into a helper
20. Facile Stereoselective Synthesis and Structural Study of Camphor‐ and Fenchone‐Based Spirocyclic 1,3,4‐Oxadiazolines
21. Untargeted search and identification of metabolites of antiviral agent camphecene in rat urine by liquid chromatography and mass spectrometry and studying their distribution in organs following peroral administration of the compound
22. The main protease 3CLpro of the SARS-CoV-2 virus: how to turn an enemy into a helper
23. Molecular Modeling of Viral Type I Fusion Proteins: Inhibitors of Influenza Virus Hemagglutinin and the Spike Protein of Coronavirus
24. Development and validation of ultrafast LC–MS/MS method for quantification of anti-influenza agent camphecene in whole rat blood using dried blood spots and its application to pharmacokinetic studies
25. 2-Aryl-1-hydroxyimidazoles possessing antiviral activity against a wide range of orthopoxviruses, including the variola virusElectronic supplementary information (ESI) available. CCDC 2331158, 2331165, 2336792, 2340418, 2340435and 2340465–2340467. For ESI and crystallographic data in CIF or other electronic format see DOI: https://doi.org/10.1039/d4md00181h
26. Usnic acid based thiazole-hydrazones as multi-targeting inhibitors of a wide spectrum of SARS-CoV-2 viruses.
27. Inhibitors of the RBD-ACE-2 Found among a Wide Range of Dyes by the Immunoassay Method
28. Discovery of a new class of antiviral compounds: Camphor imine derivatives
29. Triterpenic Acid Amides as Potential Inhibitors of the SARS-CoV-2 Main Protease
30. Structure-Based Design, Synthesis, and Biological Evaluation of the Cage–Amide Derived Orthopox Virus Replication Inhibitors
31. Synthesis and biological activity of heterocyclic borneol derivatives
32. Synthesis of new heterocyclic dehydroabietylamine derivatives and their biological activity
33. Discovery of N-Containing (-)-Borneol Esters as Respiratory Syncytial Virus Fusion Inhibitors
34. (+)-Usnic Acid and Its Derivatives as Inhibitors of a Wide Spectrum of SARS-CoV-2 Viruses
35. Stability Study, Quantification Method and Pharmacokinetics Investigation of a Coumarin–Monoterpene Conjugate Possessing Antiviral Properties against Respiratory Syncytial Virus
36. Synthesis and Antiviral Properties of Camphor-Derived Iminothiazolidine-4-Ones and 2,3-Dihydrothiazoles
37. Borneol Ester Derivatives as Entry Inhibitors of a Wide Spectrum of SARS-CoV-2 Viruses
38. Design, Synthesis, and Biological Evaluation of (+)‐Camphor‐ and (−)‐Fenchone‐Based Derivatives as Potent Orthopoxvirus Inhibitors
39. Novel O-acylated amidoximes and substituted 1,2,4-oxadiazoles synthesised from (+)-ketopinic acid possessing potent virus-inhibiting activity against phylogenetically distinct influenza A viruses
40. Optimization of application schedule of camphecene, a novel anti‐influenza compound, based on its pharmacokinetic characteristics
41. Simulation of Molecular Dynamics of SARS-CoV-2 S-Protein in the Presence of Multiple Arbidol Molecules: Interactions and Binding Mode Insights
42. Synthesis and In Vitro Study of Antiviral Activity of Glycyrrhizin Nicotinate Derivatives against HIV-1 Pseudoviruses and SARS-CoV-2 Viruses
43. Triterpenic Acid Amides as Potential Inhibitors of the SARS-CoV-2 Main Protease.
44. Structure-Based Design, Synthesis, and Biological Evaluation of the Cage–Amide Derived Orthopox Virus Replication Inhibitors.
45. Discovery of New Ginsenol-Like Compounds with High Antiviral Activity
46. New class of hantaan virus inhibitors based on conjugation of the isoindole fragment to (+)-camphor or (−)-fenchone hydrazonesv
47. Stability study of the antiviral agent camphecene in dried blood spots at different temperatures
48. Synthesis and Antiviral Activity of Camphene Derivatives against Different Types of Viruses
49. Mono- and sesquiterpenes as a starting platform for the development of antiviral drugs
50. (+)‐Camphor and (−)‐borneol derivatives as potential anti‐orthopoxvirus agents
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