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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C8753 Ceftolozane sulfateSummary: A time-dependent oxyimino cephalosporin antibacterial agent that inhibits bacterial penicillin-binding proteins (PBP3 as the primary target). -
C8754 KR-12 (human) TFASummary: The smallest antimicrobial active fragment of the human antimicrobial peptide LL-37 (corresponding to amino acids 18–29 of LL-37) -
C8761 Eflornithine hydrochlorideSummary: An irreversible ornithine decarboxylase (ODC) inhibitor -
A9068 ElbasvirSummary: Hepatitis C virus nonstructural protein 5A (HCV NS5A) inhibitor. -
B2125 RibavirinSummary: A broad-spectrum antiviral agent that interferes with viral RNA synthesis and replication. -
B8572 ChlorothalonilSummary: A broad-spectrum foliar fungicide that affects microbial communities and has reproductive toxicity. -
B8594 LipofermataSummary: A fatty acid transport protein 2 inhibitor with zinc-dependent antibacterial activity. -
B8667 CilastatinSummary: A reversible competitive renal dehydropeptidase inhibitor used to prevent imipenem metabolism. -
B8669 Ceftazidime pentahydrateSummary: A broad-spectrum antibiotic effective against Gram-positive and Gram-negative aerobic bacteria. -
B8697 CrotamitonSummary: A topical medication used to treat scabies and relieve skin itching.

