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Synthesis, molecular docking, and in silico ADME/Tox profiling studies of new 1-aryl-5-(3-azidopropyl)indol-4-ones: Potential inhibitors of SARS CoV-2 main protease

Francisco Xavier Domínguez-Villa, Noemi Angeles Durán-Iturbide, José Gustavo Ávila‐Zárraga

2020Bioorganic Chemistry119 citationsDOIOpen Access PDF

Topics & Concepts

ADMEIn silicoChemistryPharmacologyDocking (animal)Lipinski's rule of fivePharmacokineticsBioavailabilityProteaseSevere acute respiratory syndrome coronavirus 2 (SARS-CoV-2)Computational biologyDrugCoronavirus disease 2019 (COVID-19)BiochemistryEnzymeBiologyVeterinary medicineGeneMedicineDiseaseInfectious disease (medical specialty)PathologyComputational Drug Discovery MethodsSynthesis and biological activityClick Chemistry and Applications
Synthesis, molecular docking, and in silico ADME/Tox profiling studies of new 1-aryl-5-(3-azidopropyl)indol-4-ones: Potential inhibitors of SARS CoV-2 main protease | Litcius