Ivermectin inhibits importin-α/β-dependent nuclear import of viral proteins
69,71,72,78, shows spike-ACE2 disruption at 1nM with microfluidic diffusional sizing
36, binds to glycan sites on the SARS-CoV-2 spike protein preventing interaction with blood and epithelial cells and inhibiting hemagglutination
39,79, shows dose-dependent inhibition of wildtype and omicron variants
34, exhibits dose-dependent inhibition of lung injury
59,64, may inhibit SARS-CoV-2 via IMPase inhibition
35, may inhibit SARS-CoV-2 induced formation of fibrin clots resistant to degradation
8, inhibits SARS-CoV-2 3CL
pro52, may inhibit SARS-CoV-2 RdRp activity
27, may minimize viral myocarditis by inhibiting NF-κB/p65-mediated inflammation in macrophages
58, may be beneficial for COVID-19 ARDS by blocking GSDMD and NET formation
80, may interfere with SARS-CoV-2's immune evasion via ORF8 binding
3, may inhibit SARS-CoV-2 by disrupting CD147 interaction
81-84, shows protection against inflammation, cytokine storm, and mortality in an LPS mouse model sharing key pathological features of severe COVID-19
57,85, may be beneficial in severe COVID-19 by binding IGF1 to inhibit the promotion of inflammation, fibrosis, and cell proliferation that leads to lung damage
7, may minimize SARS-CoV-2 induced cardiac damage
38,46, increases Bifidobacteria which play a key role in the immune system
86, has immunomodulatory
49 and anti-inflammatory
68,87 properties, and has an extensive and very positive safety profile
88.