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Preclinical characterization of an intravenous coronavirus 3CL protease inhibitor for the potential treatment of COVID19
- Source :
- bioRxiv, Nature Communications, Vol 12, Iss 1, Pp 1-17 (2021)
- Publication Year :
- 2021
-
Abstract
- COVID-19 caused by the SARS-CoV-2 virus has become a global pandemic. 3CL protease is a virally encoded protein that is essential across a broad spectrum of coronaviruses with no close human analogs. PF-00835231, a 3CL protease inhibitor, has exhibited potent in vitro antiviral activity against SARS-CoV-2 as a single agent. Here we report, the design and characterization of a phosphate prodrug PF-07304814 to enable the delivery and projected sustained systemic exposure in human of PF-00835231 to inhibit coronavirus family 3CL protease activity with selectivity over human host protease targets. Furthermore, we show that PF-00835231 has additive/synergistic activity in combination with remdesivir. We present the ADME, safety, in vitro, and in vivo antiviral activity data that supports the clinical evaluation of PF-07304814 as a potential COVID-19 treatment.
- Subjects :
- Indoles
Science
medicine.medical_treatment
viruses
General Physics and Astronomy
Pharmacology
medicine.disease_cause
General Biochemistry, Genetics and Molecular Biology
Virus
Article
Mice
In vivo
Coronavirus 229E, Human
Leucine
Chlorocebus aethiops
medicine
Animals
Humans
Protease inhibitor (pharmacology)
skin and connective tissue diseases
Infusions, Intravenous
Vero Cells
Coronavirus 3C Proteases
Coronavirus
ADME
Multidisciplinary
Protease
Alanine
Chemistry
SARS-CoV-2
fungi
COVID-19
Drug Synergism
General Chemistry
Prodrug
In vitro
Adenosine Monophosphate
Pyrrolidinones
respiratory tract diseases
COVID-19 Drug Treatment
body regions
Disease Models, Animal
Coronavirus Protease Inhibitors
Severe acute respiratory syndrome-related coronavirus
Drug Design
Drug Therapy, Combination
HeLa Cells
Subjects
Details
- ISSN :
- 20411723
- Volume :
- 12
- Issue :
- 1
- Database :
- OpenAIRE
- Journal :
- Nature communications
- Accession number :
- edsair.doi.dedup.....a752e17863847bd64acf1c506536d2c9