β-Lactam–cannabinoid molecules combine antibacterial action with oxidative-stress control.
This case uses recombinant YidR protein with aluminum hydroxide to reduce Klebsiella and E. coli mastitis in dairy cows.
Western blot and ELISA detect commensal bacteria-specific antibodies for earlier B cell malignancy diagnosis and relapse detection.
Combining nitroimidazole or nitrofuran prodrugs with low-MIC antibiotics helps eradicate hypoxic biofilms and reduce infection recurrence.
Omadacycline combines modified minocycline chemistry with IV-to-oral dosing to target resistant CABP while limiting adverse events.
See how Lactococcus lactis JCM5805 supports skin resistance by suppressing pathogens and increasing antibacterial gene expression.
The combination targets B-cell activity and CNS protein synthesis to interrupt amyloid and prion formation.
Linked heterologous subunits enable precise non-palindromic DNA cleavage for targeted recombination with less genome-wide toxicity.
PD1 and LAG3 binders reduce pre-existing antibody binding and support T-cell activation.
This case uses the MEK-inhibitor metabolite PD-0184264 to extend treatment to 72 hours against resistant viral and bacterial infections.
This case uses substituted mannosides to bind FimH, disrupt bacterial adhesion, and address antibiotic-resistant UTIs.
This case combines three to twenty bacterial species, led by L. crispatus, to restore the vaginal microbiome and reduce BV recurrence.
A localized dimethylpropylamino substitution creates a minocycline analogue with at least 93.7% clinical success in resistant infections.
Recombinant domain merging improves Staphylococcus killing and protein stability while limiting effects on beneficial microflora.
Electrostatic API binding and ion-triggered release help deliver therapeutic antimicrobial concentrations to chronic wound biofilms.
This case combines antigen delivery with LMP1 and IPS1 fusion sequences to strengthen cellular immunity against cancer and infection.
This case uses α- and β-amyrin pentacyclic triterpenes to inhibit furin, limiting pathogen activation without fragile peptidic inhibitors.
This case uses heterocyclic and sulfonamide structure changes to support STAT3 inhibition with improved solubility and cellular uptake.