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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BA1855 AlisporivirSummary: Alisporivir (Debio-025) is a procyclin inhibitor. -
BA1856 OmbitasvirSummary: Ombitasvir is an inhibitor. -
BA1857 EIDD-2749Summary: EIDD-2749 (4'-Fluorouridine) is an orally effective inhibitor. -
BA1858 GSK-A1Summary: GSK-A1 is a selective type III phosphatidylinositol 4-kinase PI4KA inhibitor. -
BA1859 PeretinoinSummary: Peretinoin is an orally administered non-cyclic retinoid with a vitamin A-like structure that targets retinoid nuclear receptors, such as and ... -
BA1860 2-C-MethyladenosineSummary: 2'-C-Methyladenosine is an inhibitor of hepatitis C virus replication. -
BA1861 OglufanideSummary: Oglufanide (H-Glu-Trp-OH) is a dipeptide immunomodulator isolated from calf thymus that inhibits vascular endothelial growth factor. -
BA1862 NM107Summary: NM107 (2'-C-Methylcytidine) is a nucleoside inhibitor of hepatitis C virus NS5B polymerase. -
BA1863 ITX5061Summary: The ITX5061 is a Type II inhibitor. -
BA1864 R-1479Summary: R-1479 (4'-Azidocytidine) is a nucleoside analog that is a specific RNA-dependent RNA polymerase inhibitor.

