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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BA1930 AurothioglucoseSummary: Aurothioglucose (Goldthioglucose) contains monovalent gold ions and is a potent active site inhibitor of (thioredoxin reductase 1). -
BA1931 EmivirineSummary: Emivirine (MKC-442) is a potent inhibitor of non-nucleoside reverse transcriptases with values of 0.20 and 0.01 μM for dTTP- and dGTP-dependent DNA or RNA polymerase activity, respectively. -
BA1932 APOBEC3G-IN-1Summary: APOBEC3G-IN-1 (MN136.0185) is a potent inhibitor. -
BA1934 NSC727447Summary: NSC727447 is a ribonuclease H (RnaseH) inhibitor of -1 and -2. -
BA1935 UlonivirineSummary: Ulonivirine (MK-8507) is an orally active non-nucleoside reverse transcriptase inhibitor with high antiviral activity. -
BA1936 BellidifolinSummary: Bellidifolin is a xanthone (xanthone) compound extracted from the stems of swertia, which has hepatoprotective, hypoglycemic, antioxidant, anti-inflammatory and antitumor effects. -
BA1937 Ingenol-3-palmitateSummary: Ingenol-3-palmitate is a diterpene of Euphorbia, a natural product that can be isolated from the root. -
BA1938 WilfortrineSummary: Wilfortrine is a bioactive sesquiterpene alkaloid. -
BA1939 PseudothymidineSummary: C-nucleoside (C-nucleosid) analogs of thymidine. -
BA1940 PYR01Summary: PYR01 is a potent non-nucleoside reverse transcriptase inhibitor.

