Salmonella typhimurium O-4 inhibitors are a class of chemical compounds that specifically target Salmonella enterica serovar Typhimurium, focusing on its O-antigen structure, particularly the O-4 antigen. The O-antigen is part of the lipopolysaccharide (LPS) layer in the outer membrane of Gram-negative bacteria like Salmonella, and it plays a crucial role in bacterial virulence, surface recognition, and immune evasion. The O-4 antigen is a specific polysaccharide structure that distinguishes this serovar from other Salmonella strains. Inhibitors of Salmonella typhimurium O-4 are designed to disrupt the biosynthesis, assembly, or function of the O-antigen, thereby impairing the bacterium's ability to interact with its environment, survive host defenses, or colonize specific niches. These inhibitors are valuable tools for studying the structure and function of bacterial outer membranes and the role of surface antigens in pathogenicity.
Salmonella typhimurium O-4 inhibitors may interfere with various stages of O-antigen biosynthesis, including the enzymes responsible for assembling sugar monomers into the polysaccharide chain or those involved in linking the O-antigen to the LPS core. Some inhibitors are designed to mimic substrate molecules, competitively blocking enzyme active sites, while others might act by destabilizing the overall LPS structure. By inhibiting the production or function of the O-4 antigen, these compounds allow researchers to explore how Salmonella Typhimurium adapts to its host environment and how its surface structures contribute to bacterial physiology and virulence. Such studies are critical for understanding the molecular mechanisms of bacterial survival and may provide insights into how outer membrane components regulate bacterial behavior in different environmental contexts, including host interactions and immune responses.
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Ciprofloxacin | 85721-33-1 | sc-217900 | 1 g | $43.00 | 8 | |
Inhibits DNA gyrase, blocking DNA replication and repair. | ||||||
Rifampicin | 13292-46-1 | sc-200910 sc-200910A sc-200910B sc-200910C | 1 g 5 g 100 g 250 g | $97.00 $328.00 $676.00 $1467.00 | 6 | |
Inhibits RNA polymerase, halting RNA synthesis. | ||||||
Trimethoprim | 738-70-5 | sc-203302 sc-203302A sc-203302B sc-203302C sc-203302D | 5 g 25 g 250 g 1 kg 5 kg | $67.00 $161.00 $255.00 $721.00 $3401.00 | 4 | |
Blocks dihydrofolate reductase, interfering with DNA synthesis. | ||||||
Ampicillin | 69-53-4 | sc-210812 sc-210812A sc-210812B sc-210812C sc-210812D | 100 mg 1 g 5 g 25 g 100 g | $31.00 $101.00 $153.00 $115.00 $408.00 | 11 | |
Disrupts cell wall synthesis by inhibiting transpeptidases. | ||||||
Chloramphenicol | 56-75-7 | sc-3594 | 25 g | $90.00 | 10 | |
Inhibits bacterial protein synthesis by binding to 50S ribosome subunit. | ||||||
Sulfamethoxazole | 723-46-6 | sc-208405 sc-208405A sc-208405B sc-208405C | 10 g 25 g 50 g 100 g | $37.00 $55.00 $69.00 $109.00 | 5 | |
Interferes with folate synthesis, essential for bacterial growth. | ||||||
Ceftriaxone, Disodium Salt, Hemiheptahydrate | 104376-79-6 | sc-211050 sc-211050A | 1 g 5 g | $179.00 $449.00 | 1 | |
Blocks cell wall synthesis by binding to penicillin-binding proteins. | ||||||
Tetracycline | 60-54-8 | sc-205858 sc-205858A sc-205858B sc-205858C sc-205858D | 10 g 25 g 100 g 500 g 1 kg | $63.00 $94.00 $270.00 $417.00 $634.00 | 6 | |
Inhibits protein synthesis by binding to 30S ribosome subunit. | ||||||
Gentamicin sulfate | 1405-41-0 | sc-203334 sc-203334A sc-203334F sc-203334B sc-203334C sc-203334D sc-203334E | 1 g 5 g 50 g 100 g 1 kg 2.5 kg 7.5 kg | $56.00 $179.00 $509.00 $725.00 $1836.00 $2652.00 $6248.00 | 3 | |
Disrupts bacterial protein synthesis by binding to 30S ribosome subunit. | ||||||
Azithromycin | 83905-01-5 | sc-254949 sc-254949A sc-254949B sc-254949C sc-254949D | 25 mg 50 mg 500 mg 1 g 5 g | $52.00 $103.00 $260.00 $364.00 $728.00 | 17 | |
Binds to 50S ribosome subunit, inhibiting protein synthesis. | ||||||