Synthesis, SARS-CoV-2 main protease inhibition, molecular docking and in silico ADME studies of furanochromene-quinoline hydrazone derivatives-Reference-Cited by-同舟云学术

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Synthesis, SARS-CoV-2 main protease inhibition, molecular docking and in silico ADME studies of furanochromene-quinoline hydrazone derivatives

Published:2024-04 Issue: Volume:102 Page:129679
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Shellenberger Blake M.,Basile Olivia N.,Cassel Joel^ORCID,Olsen Morgan R.,Salvino Joseph M.,Montaner Luis J.,Tietjen Ian^ORCID,Henry Geneive E.

Funder

Canadian Institutes of Health Research

Publisher

Elsevier BV

Reference55 articles.

1. A review of SARS-CoV-2 disease (COVID-19): pandemic in our time;Al-Awwal;Pathogens,2022

2. Characteristics of SARS-CoV-2 and COVID-19;Hu;Nat Rev Microbiol,2021

3. The inclusive review on SARS–CoV–2 biology, epidemiology, diagnosis, and potential management options;Parikhani;Curr Microbiol,2021

4. Therapeutic advances in COVID-19;Murakami;Nat Rev Nephrol,2023

5. Therapeutic strategies for COVID-19: progress and lessons learned;Li;Nat Rev Drug Discov,2023

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Synthetic approaches for quinoline heterocycles fused at face b: A review;Synthetic Communications;2024-08-19

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