A combination therapy using auranofin, ouabain, emetine, niclosamide, and fluoxetine suppresses EV71 replication through synergistic activity.
Small-molecule entry inhibitors bind to the SARS-CoV-2 spike receptor binding domain interface to block viral attachment.
OZ418 ozonides suppress cytomegalovirus replication while reducing bone marrow and kidney toxicity associated with standard antiviral therapies.
Formula I compounds disrupt HBV capsid assembly to reduce viral load, overcoming drug resistance and tolerability issues in chronic infection treatment.
Covalent CDK7 inhibitors block host cell machinery to treat resistant herpesvirus and papillomavirus infections without triggering rapid drug resistance.
Modified cyclosporine analogues bind host cyclophilin A to inhibit viral replication while reducing immunosuppressive side effects.
Young barley grass composition increases regulatory T cells while suppressing excessive immune responses to prevent autoimmune diseases.
Small molecule compounds modulate hepatitis B core protein assembly to inhibit viral replication and reduce HBV DNA levels.