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.
| 製品名 | CAS # | カタログ # | 数量 | 価格 | 引用文献 | レーティング |
|---|---|---|---|---|---|---|
Ciprofloxacin | 85721-33-1 | sc-217900 | 1 g | $42.00 | 8 | |
DNAジャイレースを阻害し、DNAの複製と修復を阻害する。 | ||||||
Rifampicin | 13292-46-1 | sc-200910 sc-200910A sc-200910B sc-200910C | 1 g 5 g 100 g 250 g | $95.00 $322.00 $663.00 $1438.00 | 6 | |
RNAポリメラーゼを阻害し、RNA合成を停止させる。 | ||||||
Trimethoprim | 738-70-5 | sc-203302 sc-203302A sc-203302B sc-203302C sc-203302D | 5 g 25 g 250 g 1 kg 5 kg | $66.00 $158.00 $204.00 $707.00 $3334.00 | 4 | |
ジヒドロ葉酸還元酵素を阻害し、DNA合成を妨げる。 | ||||||
Ampicillin | 69-53-4 | sc-210812 sc-210812A sc-210812B sc-210812C sc-210812D | 100 mg 1 g 5 g 25 g 100 g | $30.00 $99.00 $150.00 $215.00 $400.00 | 11 | |
トランスペプチダーゼを阻害することにより細胞壁合成を阻害する。 | ||||||
Chloramphenicol | 56-75-7 | sc-3594 | 25 g | $53.00 | 10 | |
50Sリボソームサブユニットに結合して細菌のタンパク質合成を阻害する。 | ||||||
Sulfamethoxazole | 723-46-6 | sc-208405 sc-208405A sc-208405B sc-208405C | 10 g 25 g 50 g 100 g | $36.00 $54.00 $68.00 $107.00 | 5 | |
細菌の増殖に不可欠な葉酸の合成を阻害する。 | ||||||
Ceftriaxone, Disodium Salt, Hemiheptahydrate | 104376-79-6 | sc-211050 sc-211050A | 1 g 5 g | $175.00 $440.00 | 1 | |
ペニシリン結合タンパク質に結合して細胞壁合成を阻害する。 | ||||||
Tetracycline | 60-54-8 | sc-205858 sc-205858A sc-205858B sc-205858C sc-205858D | 10 g 25 g 100 g 500 g 1 kg | $62.00 $92.00 $265.00 $409.00 $622.00 | 6 | |
30Sリボソームサブユニットに結合し、タンパク質合成を阻害する。 | ||||||
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 | $55.00 $175.00 $499.00 $720.00 $1800.00 $2600.00 $6125.00 | 3 | |
30Sリボソームサブユニットに結合し、細菌のタンパク質合成を阻害する。 | ||||||
Azithromycin | 83905-01-5 | sc-254949 sc-254949A sc-254949B sc-254949C sc-254949D | 25 mg 50 mg 500 mg 1 g 5 g | $51.00 $101.00 $255.00 $357.00 $714.00 | 17 | |
50Sリボソームサブユニットに結合し、タンパク質合成を阻害する。 | ||||||