See how psychrophilic protease enzymes embedded in fabric inactivate viruses and bacteria on co
A bictegravir, emtricitabine, and tenofovir alafenamide regimen addresses limited HIV prophylaxis options with timed post-exposure protection.
Compounds targeting SARS-CoV-2 Mpro and PLpro inhibit viral replication and immune suppression, supporting COVID-19 treatment or prevention.
A multi-herb extract targets severe COVID-19 complications by improving blood oxygen, easing pleural effusion, and supporting vital organ stability.
A nucleoside phosphate prodrug improves in vivo phosphorylation, boosting coronavirus inhibition and speeding viral clearance in COVID-19 treatment.
Nitroxoline-based cysteine protease inhibitors block coronavirus entry and replication while limiting host cell toxicity through selective cathepsin B inhibition.
Overlapping peptide libraries and antigen-presenting cells enable safe expansion of HPV-specific T cells from naive donors without live viruses.
A modified herbal composition blocks spike-ACE2 binding and 3CL protease while reducing inflammation, thrombosis, and lung damage.
A ten-herb TCM composition inhibits spike-ACE2 binding, reduces cytokine release, and slows pulmonary embolism and fibrosis progression.
Combining NS5B and NS5A inhibitors in one fixed-dose therapy improves pan-genotypic HCV suppression while limiting resistance and treatment complexity.
A Neurolaena lobata leaf tincture blocks DHODH and viral pyrimidine supply while avoiding the cytotoxicity seen with synthetic inhibitors.
Small-molecule protease inhibitors use targeted structural tuning to balance potency, selectivity, and oral bioavailability for cancer and viral therapy.
Substituted nucleoside compounds inhibit SARS-CoV-2 RNA polymerase to treat or prevent infection while broadening usable drug forms.
An intranasal peptide conjugate blocks viral entry and reduces SARS-CoV-2 or paramyxovirus transmission without prolonged isolation.
A WS-635 composition case showing how broad coronavirus inhibition can improve treatment effectiveness against SARS-CoV-2 and related infections.
Dose-adjusted maribavir regimens help treat CMV in transplant recipients while managing interactions with CYP3A4 inducers and co-medications.
Computationally identified EC-CREs boost endothelial-specific gene expression, enabling lower vector doses and safer gene therapy.
A five-herb composition is formulated to inhibit SARS-CoV-2 replication in Vero cells and support coronavirus treatment research.
Combining an HIV-1 integrase inhibitor with other anti-HIV agents helps treat resistant HIV strains while addressing side effects and cross-resistance.
Botanical extracts with extracellular and intracellular antiviral action are combined to boost HSV-1 inhibition and reduce resistance risk.
A multi-herb composition inhibits spike-ACE2 binding to block wild-type and variant SARS-CoV-2 entry with minimal cytotoxicity.
Pharmaceutical combinations target RNA viral infection while lowering lung viral titers, neutrophil density, and necrotized cell counts.
Standardized nasturtium and horseradish powders improve oral RSV inhibition while reducing side-effect risks of supportive care.
Cationized nucleases paired with dendrimers improve cell entry and RNase inhibitor evasion to disrupt viral RNA replication.
Dose adjustment and drug-level monitoring help maribavir maintain CMV treatment efficacy while limiting interactions with inducers and co-medications.
An NKG2D CAR with 4-1BB and CD3-zeta domains helps engineered T cells target resistant solid tumors more effectively.
A defined monolayer culture platform replaces embryoid body and serum-based steps to scale homogeneous hematopoietic cell production.