Dipeptides stabilize antibodies against protease degradation in intestinal fluid, enabling oral delivery.
Nonfucosylated anti-CD70 antibodies deplete cancer cells via enhanced ADCC activity.
Targeting the active GTP-bound state prevents resistance mutations at Y96, H95, and R68 that typically render standard RAS(OFF) inhibitors ineffective.
A humanized IgG1 monoclonal antibody binds to carcinoma antigens and mediates cytotoxicity against tumor cells.
Subcutaneous anti-CD38 antibodies address high toxicity and inconvenient intravenous administration in multiple myeloma therapy.
Proteasome inhibitors accumulate pro-apoptotic proteins in reactivated HIV cells to eliminate the latent reservoir.
Retinylamine derivatives conjugated with amino acids sequester toxic all-trans-retinal to preserve retinal structure.
Combining loperamide with proteasome inhibitors overcomes solid tumor resistance, reducing side effects while maintaining therapeutic impact.
Cysteine derivatives form cyclic thiazolidines with acetaldehyde, resolving blood aldehyde buildup and Asian flushing syndrome.
Dipeptide compounds inhibit TGF-beta activity with enhanced plasma stability, resolving adverse effects from non-specific inhibition.
A sulfomaleimide linker covalently attaches drugs to antibodies via irreversible bonds.
Segmented PROTAC molecules bridge E3 ligases to induce proteasomal degradation, reducing inhibitor concentration and off-target effects.
Modified phenylalanine dipeptides reduce toxic side effects while effectively treating hepatitis B and HIV infections.
Analyzes patient SNPs to tailor RAAS pathway pharmaceuticals, resolving contradictions in ACE2 modulation for pre- and post-infection scenarios.
CD19 binding agents deplete malignant B-cells, reducing relapse rates and improving survival outcomes.