Date published: 2025-9-11

021-6093-6350

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Salmonella typhimurium 0-4 抑制因子

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.

产品名称CAS #产品编号数量价格应用排名

Ciprofloxacin

85721-33-1sc-217900
1 g
¥474.00
8
(1)

抑制 DNA 回旋酶,阻碍 DNA 复制和修复。

Rifampicin

13292-46-1sc-200910
sc-200910A
sc-200910B
sc-200910C
1 g
5 g
100 g
250 g
¥1072.00
¥3633.00
¥7480.00
¥16224.00
6
(1)

抑制 RNA 聚合酶,停止 RNA 合成。

Trimethoprim

738-70-5sc-203302
sc-203302A
sc-203302B
sc-203302C
sc-203302D
5 g
25 g
250 g
1 kg
5 kg
¥745.00
¥1783.00
¥2302.00
¥7976.00
¥37614.00
4
(1)

阻断二氢叶酸还原酶,干扰 DNA 合成。

Ampicillin

69-53-4sc-210812
sc-210812A
sc-210812B
sc-210812C
sc-210812D
100 mg
1 g
5 g
25 g
100 g
¥338.00
¥1117.00
¥1692.00
¥2426.00
¥4513.00
11
(0)

通过抑制转肽酶破坏细胞壁合成。

Chloramphenicol

56-75-7sc-3594
25 g
¥598.00
10
(1)

通过与 50S 核糖体亚基结合抑制细菌蛋白质合成。

Sulfamethoxazole

723-46-6sc-208405
sc-208405A
sc-208405B
sc-208405C
10 g
25 g
50 g
100 g
¥406.00
¥609.00
¥767.00
¥1207.00
5
(0)

干扰细菌生长所必需的叶酸合成。

Ceftriaxone, Disodium Salt, Hemiheptahydrate

104376-79-6sc-211050
sc-211050A
1 g
5 g
¥1974.00
¥4964.00
1
(1)

通过与青霉素结合蛋白结合阻止细胞壁合成。

Tetracycline

60-54-8sc-205858
sc-205858A
sc-205858B
sc-205858C
sc-205858D
10 g
25 g
100 g
500 g
1 kg
¥699.00
¥1038.00
¥2990.00
¥4614.00
¥7017.00
6
(1)

通过与 30S 核糖体亚基结合抑制蛋白质合成。

Gentamicin sulfate

1405-41-0sc-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
¥621.00
¥1974.00
¥5630.00
¥8123.00
¥20308.00
¥29333.00
¥69102.00
3
(1)

通过与 30S 核糖体亚基结合破坏细菌蛋白质合成。

Azithromycin

83905-01-5sc-254949
sc-254949A
sc-254949B
sc-254949C
sc-254949D
25 mg
50 mg
500 mg
1 g
5 g
¥575.00
¥1139.00
¥2877.00
¥4028.00
¥8055.00
17
(1)

与 50S 核糖体亚基结合,抑制蛋白质合成。