26 results on '"Corona, Angela"'
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2. Drug repurposing screen to identify inhibitors of the RNA polymerase (nsp12) and helicase (nsp13) from SARS-CoV-2 replication and transcription complex
3. Suramin inhibits SARS-CoV-2 nucleocapsid phosphoprotein genome packaging function
4. Diketo acid inhibitors of nsp13 of SARS-CoV-2 block viral replication
5. Naïve antibody library derived monoclonal antibody against VP35 of Ebola virus
6. Versatile anti-infective properties of pyrido- and dihydropyrido[2,3-d]pyrimidine-based compounds
7. Broad-spectrum coronavirus 3C-like protease peptidomimetic inhibitors effectively block SARS-CoV-2 replication in cells: Design, synthesis, biological evaluation, and X-ray structure determination
8. Ebola virus disease: In vivo protection provided by the PAMP restricted TLR3 agonist rintatolimod and its mechanism of action
9. Drug Repurposing Screen to Identify Inhibitors of Sars-Cov-2 Minimal Functional Replication and Transcription Complex
10. Easy access to α-ketoamides as SARS-CoV-2 and MERS Mpro inhibitors via the PADAM oxidation route
11. Cynarin blocks Ebola virus replication by counteracting VP35 inhibition of interferon-beta production
12. Discovery of dihydroxyindole-2-carboxylic acid derivatives as dual allosteric HIV-1 Integrase and Reverse Transcriptase associated Ribonuclease H inhibitors
13. Ribonuclease H, an unexploited target for antiviral intervention against HIV and hepatitis B virus
14. Chromenone derivatives as a versatile scaffold with dual mode of inhibition of HIV-1 reverse transcriptase-associated Ribonuclease H function and integrase activity
15. Meeting report: Fourth Summer School on Innovative Approaches for Identification of Antiviral Agents (IAAASS)
16. Novel natural non-nucleoside inhibitors of HIV-1 reverse transcriptase identified by shape- and structure-based virtual screening techniques
17. Insights into the homo-oligomerization properties of N-terminal coiled-coil domain of Ebola virus VP35 protein
18. Natural product-inspired esters and amides of ferulic and caffeic acid as dual inhibitors of HIV-1 reverse transcriptase
19. Sennoside A, derived from the traditional chinese medicine plant Rheum L., is a new dual HIV-1 inhibitor effective on HIV-1 replication
20. New insights into the interaction between pyrrolyl diketoacids and HIV-1 integrase active site and comparison with RNase H
21. (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
22. Antiretroviral activity of metal-chelating HIV-1 integrase inhibitors
23. Indoleamine 2,3-dioxygenase inhibition attenuates lipopolysaccharide induced persistent microglial activation and depressive-like complications in fractalkine receptor (CX3CR1)-deficient mice
24. Development of a series of 3-hydroxyquinolin-2(1H)-ones as selective inhibitors of HIV-1 reverse transcriptase associated RNase H activity
25. Design and Synthesis of New Isatin Derivatives as HIV-1 Reverse Transcriptase Associated Ribonuclease H Inhibitors
26. Broad-spectrum coronavirus 3C-like protease peptidomimetic inhibitors effectively block SARS-CoV-2 replication in cells: Design, synthesis, biological evaluation, and X-ray structure determination
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