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Anti-infection

Anti-infectives are agents that eliminate or inhibit the spread of infectious organisms, encompassing antibiotics, antifungals, antivirals, and antiprotozoals.

Antibiotics are a class of antimicrobial agents specifically designed to target bacterial pathogens. They exert their effects by interfering with essential bacterial processes such as cell wall synthesis, protein synthesis, nucleic acid replication, and metabolic pathways, thereby either inhibiting bacterial growth or inducing bacterial death.

Antifungals are antimicrobial agents employed to combat fungal infections (mycoses) in humans and animals. Common antifungal classes include azoles, polyenes, echinocandins, and allylamines, which function by disrupting unique fungal structures or pathways, such as the synthesis or integrity of ergosterol-containing cell membranes and β-glucan-based cell walls, or by interfering with nucleic acid or protein synthesis.

Antivirals are compounds developed to inhibit the replication and spread of viruses within host organisms. Antivirals typically act by blocking viral entry, genome replication, protein processing, or virion assembly and release. Representative examples include nucleoside analogs, protease inhibitors, and neuraminidase inhibitors.

Antiprotozoals are drugs used to treat infections caused by protozoan parasites, including malaria, amebiasis, giardiasis, and trypanosomiasis. They act through a variety of mechanisms, including inhibition of nucleic acid synthesis, interference with mitochondrial function, and disruption of heme detoxification pathways in susceptible parasites.

Items 1681-1690 of 1844

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  1. Urolithin M5
    C8591 Urolithin M5
    Summary: A natural neuraminidase (NA) inhibitor isolated from olive leaves
      ≥40.2 mg/mL
  2. Antimycin A4
    C8711 Antimycin A4
    Summary: An inhibitor of ATP-citrate lyase
      Soluble in DMSO
  3. Faropenem sodium
    C8712 Faropenem sodium
    Summary: A penem antibiotic
      ≥51.7 mg/mL
  4. Grazoprevir hydrate
    C8713 Grazoprevir hydrate
    Summary: A HCV protease inhibitor
      ≥51.1 mg/mL
  5. Neticonazole hydrochloride
    C8715 Neticonazole hydrochloride
    Summary: An imidazole antifungal
      ≥46.5 mg/mL
  6. Sodium dicloxacillin monohydrate
    C8716 Sodium dicloxacillin monohydrate
    Summary: A narrow-spectrum β-lactam antibiotic of the penicillin class, which can inhibit the growth of Gram-positive bacteria such as methicillin-sensitive Staphylococcus aureus (MSSA), with bacterial penicillin-binding proteins (PBPs) as its target of action.
  7. Acetylsalicylic acid lithium
    C8731 Acetylsalicylic acid lithium
    Summary: An orally active, irreversible cyclooxygenase (COX-1 and COX-2) inhibitor, also commonly used to induce gastric ulcer models.
  8. (+)-Ofloxacin
    C8735 (+)-Ofloxacin
    Summary: The R-enantiomer of the fluoroquinolone antibacterial drug ofloxacin; forms a complex by binding bacterial DNA and DNA topoisomerase II (DNA gyrase), inhibiting DNA strand annealing and bacterial replication
      insoluble in DMSO; insoluble in EtOH; ≥25.35 mg/mL
  9. 8-Epidiosbulbin E acetate
    N2890 8-Epidiosbulbin E acetate
    Summary: A furan compound with broad-spectrum plasmid-curing activity against multiple multidrug-resistant bacteria, including vancomycin-resistant enterococci
      ≥50.5 mg/mL
  10. Doxycycline hydrochloride
    C8734 Doxycycline hydrochloride
    Summary: A broad-spectrum tetracycline antibiotic that primarily inhibits the bacterial ribosomal 30S subunit, thereby blocking protein synthesis

Items 1681-1690 of 1844

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