SARS-CoV-2 Inhibitors

InformationAtovaquone (Atavaquone) is a medication used to treat or prevent for pneumocystis pneumonia, toxoplasmosis, malaria, and babesia.In vitroAtovaquone (atavaquone) is a chemical compound that belongs to the class of naphthalenes. Atovaquone

InformationAzithromycin (CP-62993, XZ-450) is an antibiotic by inhibiting protein synthesis, used for the treatment of bacterial infections.In vitroAzithromycin reduces about 40% of IL-8 mRNA and protein expression in cystic fibrosis (CF) cells

Bepotastine is a non-sedating, selective antagonist of histamine 1 (H1) receptor with pIC50 of 5.7.Bepotastine Beslilate is a histamine H1 receptor anatagonist.

Bepotastine is a non-sedating, selective antagonist of histamine 1 (H1) receptor with pIC50 of 5.7.Bepotastine Beslilate is a histamine H1 receptor anatagonist.

Bepotastine is a non-sedating, selective antagonist of histamine 1 (H1) receptor with pIC50 of 5.7.Bepotastine Beslilate is a histamine H1 receptor anatagonist.

Bepotastine is a non-sedating, selective antagonist of histamine 1 (H1) receptor with pIC50 of 5.7.Bepotastine Beslilate is a histamine H1 receptor anatagonist.

Bepotastine is a non-sedating, selective antagonist of histamine 1 (H1) receptor with pIC50 of 5.7.Bepotastine Beslilate is a histamine H1 receptor anatagonist.

InformationBepotastine Besilate (TAU 284) is a non-sedating, selective antagonist ofhistamine 1 (H1)receptor withpIC50of 5.7.In vitroThe flux ratios of [14C]Bepotastine (5 μM) in LLC-GA5-COL150 cells are significantly greater than those in LLC-PK1,

InformationCamostat (FOY-305, FOY-S980) is a trypsin-like protease inhibitor, inhibits airway epithelial sodium channel (ENaC) function withIC50of 50 nM, less potent to trpsin, prostasin and matriptase.In vitroCamostat (30 μM) prolongs attenuation

InformationCarfilzomib (PR-171) is an irreversibleproteasomeinhibitor withIC50of &lt:5 nM in ANBL-6 cells, displayed preferential in vitro inhibitory potency against the ChT-L activity in the β5 subunit, but little or no effect on the PGPH and T-L

Chloroquine Phosphate.

Potent NS3/4A protease inhibitor.