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.
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C8715 Neticonazole hydrochlorideSummary: An imidazole antifungal -
C8716 Sodium dicloxacillin monohydrateSummary: 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. -
C8731 Acetylsalicylic acid lithiumSummary: An orally active, irreversible cyclooxygenase (COX-1 and COX-2) inhibitor, also commonly used to induce gastric ulcer models. -
C8735 (+)-OfloxacinSummary: 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 -
N2890 8-Epidiosbulbin E acetateSummary: A furan compound with broad-spectrum plasmid-curing activity against multiple multidrug-resistant bacteria, including vancomycin-resistant enterococci -
C8734 Doxycycline hydrochlorideSummary: A broad-spectrum tetracycline antibiotic that primarily inhibits the bacterial ribosomal 30S subunit, thereby blocking protein synthesis -
N2889 HexadecanamideSummary: A fatty acid amide derived from palmitic acid, commonly used to study its anti-inflammatory and neuroprotective effects -
C3816 PentoxifyllineSummary: A phosphodiesterase (PDE, especially PDE IV) inhibitor

