Date published: 2025-11-7

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Salmonella typhimurium 0-4 Inhibidores

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.

Nombre del productoNÚMERO DE CAS #Número de catálogoCantidadPrecioMENCIONESClasificación

Ciprofloxacin

85721-33-1sc-217900
1 g
¥474.00
8
(1)

Inhibe la ADN girasa, bloqueando la replicación y reparación del ADN.

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)

Inhibe la ARN polimerasa, deteniendo la síntesis de ARN.

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)

Bloquea la dihidrofolato reductasa, interfiriendo en la síntesis de ADN.

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)

Altera la síntesis de la pared celular inhibiendo las transpeptidasas.

Chloramphenicol

56-75-7sc-3594
25 g
¥598.00
10
(1)

Inhibe la síntesis de proteínas bacterianas al unirse a la subunidad 50S del ribosoma.

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)

Interfiere en la síntesis del folato, esencial para el crecimiento bacteriano.

Ceftriaxone, Disodium Salt, Hemiheptahydrate

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

Bloquea la síntesis de la pared celular uniéndose a las proteínas de unión a la penicilina.

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)

Inhibe la síntesis de proteínas al unirse a la subunidad 30S del ribosoma.

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)

Interrumpe la síntesis de proteínas bacterianas al unirse a la subunidad 30S del ribosoma.

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)

Se une a la subunidad 50S del ribosoma, inhibiendo la síntesis de proteínas.