17 Results for "

Campylobacter jejuni

" in MedChemExpress (MCE) Product Catalog:
Products (17)

17 Results for "Campylobacter jejuni" in MCE Product Catalog:

1
1 Cited Publications
Cat. No.: HY-B1244
CAS No.: 551-92-8
Synonyms: 1,2-Dimethyl-5-nitroimidazole
Dimetridazole is a nitroimidazole antibiotic. Dimetridazole inhibits protein synthesis in cultures of Campylobacter jejuni. Dimetridazole is genotoxic. Dimetridazole can be used in the research of protozoal and bacterial infections .
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1
1 Cited Publications
Cat. No.: HY-B1244S
CAS No.: 64678-69-9
Synonyms: 1,2-Dimethyl-5-nitroimidazole-d3
Dimetridazole-d3 (1,2-Dimethyl-5-nitroimidazole-d3) is a deuterium labeled Dimetridazole (HY-B1244). Dimetridazole is a nitroimidazole antibiotic. Dimetridazole inhibits protein synthesis in cultures of Campylobacter jejuni. Dimetridazole is genotoxic. Dimetridazole can be used in the research of protozoal and bacterial infections .
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Cat. No.: HY-B0396
CAS No.: 161715-24-8
Synonyms: L084
Target:  

Antibiotic Bacterial OAT

Research Areas:  

Infection

Tebipenem pivoxil (L084 hydrobromide) is an orally active carbapenem Antibiotic. Tebipenem pivoxil acts as a substrate of OATP1A2 with high affinity for this transporter (Km = 41.1 μM) . Tebipenem pivoxil achieves intestinal absorption via carrier-mediated uptake and simple diffusion. Tebipenem pivoxil inhibits the growth of Gram-positive bacteria, Gram-negative bacteria, multidrug-resistant bacteria, and pathogens producing extended-spectrum β-lactamases. Tebipenem pivoxil eliminates intestinal infection pathogens and reduces mortality in septic mice. Tebipenem pivoxil can be used in research related to bacterial pneumonia, severe gastrointestinal infections, bacterial sepsis, complicated urinary tract infections, and acute pyelonephritis .
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Cat. No.: HY-N10530
CAS No.: 20768-11-0
Synonyms: Difucosyllactose ; 2′,3-Difucosyllactose
Lactodifucotetraose is a difucosylated human milk oligosaccharide. Lactodifucotetraose inhibits platelet function and the release of inflammatory factors. Lactodifucotetraose can be used for the research of *Campylobacter jejuni*-associated diarrhea and platelet-induced inflammatory processes .
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Cat. No.: HY-W007416
CAS No.: 26153-38-8
Target:  

Glycosidase Bacterial

Research Areas:  

Infection Metabolic Disease

3,5-Dihydroxybenzaldehyde is an α-glucosidase inhibitor with an IC50 of 0.47 μg/mL. 3,5-Dihydroxybenzaldehyde exerts bactericidal activity against Campylobacter jejuni, Escherichia coli O157:H7, Listeria monocytogenes and Salmonella enterica. 3,5-Dihydroxybenzaldehyde can be used in glucose metabolism-related research .
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Cat. No.: HY-B1894A
CAS No.: 111696-23-2
Synonyms: Ro 15-8075
Target:  

Antibiotic Bacterial

Research Areas:  

Infection Inflammation/Immunology

Cefetamet pivoxyl hydrochloride (Ro 15-8075) is an orally active cephalosporin Antibiotic and a prodrug of Cefetamet (HY-A0111). After ingestion, Cefetamet pivoxyl hydrochloride is hydrolyzed by gastrointestinal esterases to form Cefetamet. Cefetamet pivoxyl hydrochloride is primarily active against aerobic Gram-negative bacteria (such as Enterobacteriaceae, Neisseria, Haemophilus) and some Gram-positive bacteria (such as non-enterococcal streptococci). Cefetamet pivoxyl hydrochloride exhibits potent in vivo antibacterial activity against strains of Gram-positive bacteria (S. pyogenes) and Gram-negative bacteria (E. coli, K. pneumoniae, S. marcescens, P. vulgaris, P. mirabilis, H. influenzae) .
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Cat. No.: HY-E71216
Research Areas:  

Others

α-2,3/8-Sialyltransferase, Campylobacter jejuni (EC 2.4.99.-) is an enzyme that transfers sialic acid to nascent oligosaccharides. α-2,3/8-Sialyltransferase, Campylobacter jejuni (EC 2.4.99.-) adds sialic acid to the terminal of sialylated glycolipids (gangliosides) or to the N- or O-linked sugar chain of glycoproteins.
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Cat. No.: HY-B0396A
CAS No.: 211558-19-9
Synonyms: L084 hydrochloride
Target:  

Antibiotic Bacterial OAT

Research Areas:  

Infection

Tebipenem pivoxil hydrochloride (L084 hydrochloride) is an orally active carbapenem Antibiotic. Tebipenem pivoxil hydrochloride acts as a substrate of OATP1A2 with high affinity for this transporter (Km = 41.1 μM) . Tebipenem pivoxil hydrochloride achieves intestinal absorption via carrier-mediated uptake and simple diffusion. Tebipenem pivoxil hydrochloride inhibits the growth of Gram-positive bacteria, Gram-negative bacteria, multidrug-resistant bacteria, and pathogens producing extended-spectrum β-lactamases. Tebipenem pivoxil hydrochloride eliminates intestinal infection pathogens and reduces mortality in septic mice. Tebipenem pivoxil hydrochloride can be used in research related to bacterial pneumonia, severe gastrointestinal infections, bacterial sepsis, complicated urinary tract infections, and acute pyelonephritis .
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Cat. No.: HY-123354
CAS No.: 115812-74-3
Target:  

Bacterial

Research Areas:  

Infection

SC 44914 is a quinoxaline compound with antibacterial effects. SC-44914 has activity against Campylobacter jejuni, C. coli, and Clostridium difficile .
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Cat. No.: HY-B1244R
CAS No.: 551-92-8
Synonyms: 1,2-Dimethyl-5-nitroimidazole (Standard)
Research Areas:  

Infection

Dimetridazole (Standard) is the analytical standard of Dimetridazole (HY-B1244). This product is intended for research and analytical applications. Dimetridazole is a nitroimidazole antibiotic. Dimetridazole inhibits protein synthesis in cultures of Campylobacter jejuni. Dimetridazole is genotoxic. Dimetridazole can be used in the research of protozoal and bacterial infections .
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Cat. No.: HY-B0396R
CAS No.: 161715-24-8
Synonyms: L084 (Standard)
Research Areas:  

Infection

Tebipenem pivoxil (Standard) (L084 (Standard)) is the analytical standard of Tebipenem pivoxil (HY-B0396). This product is intended for research and analytical applications. Tebipenem pivoxil (L084 hydrobromide) is an orally active carbapenem Antibiotic. Tebipenem pivoxil acts as a substrate of OATP1A2 with high affinity for this transporter (Km = 41.1 μM) . Tebipenem pivoxil achieves intestinal absorption via carrier-mediated uptake and simple diffusion. Tebipenem pivoxil inhibits the growth of Gram-positive bacteria, Gram-negative bacteria, multidrug-resistant bacteria, and pathogens producing extended-spectrum β-lactamases. Tebipenem pivoxil eliminates intestinal infection pathogens and reduces mortality in septic mice. Tebipenem pivoxil can be used in research related to bacterial pneumonia, severe gastrointestinal infections, bacterial sepsis, complicated urinary tract infections, and acute pyelonephritis .
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Cat. No.: HY-B1894
CAS No.: 65243-33-6
Synonyms: Ro 15-8075 free base
Target:  

Antibiotic Bacterial

Research Areas:  

Infection Inflammation/Immunology

Cefetamet pivoxyl (Ro 15-8075 free base) is an orally active cephalosporin Antibiotic and a prodrug of Cefetamet (HY-A0111). After ingestion, Cefetamet pivoxyl is hydrolyzed by gastrointestinal esterases to form Cefetamet. Cefetamet pivoxyl is primarily active against aerobic Gram-negative bacteria (such as Enterobacteriaceae, Neisseria, Haemophilus) and some Gram-positive bacteria (such as non-enterococcal streptococci). Cefetamet pivoxyl exhibits potent in vivo antibacterial activity against strains of Gram-positive bacteria (S. pyogenes) and Gram-negative bacteria (E. coli, K. pneumoniae, S. marcescens, P. vulgaris, P. mirabilis, H. influenzae) .
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Cat. No.: HY-B1894AR
CAS No.: 111696-23-2
Synonyms: Ro 15-8075 (Standard)
Cefetamet pivoxil (hydrochloride) (Standard) (Ro 15-8075 (Standard)) is the analytical standard of Cefetamet pivoxil (hydrochloride) (HY-B1894A). This product is intended for research and analytical applications. Cefetamet pivoxyl hydrochloride (Ro 15-8075) is an orally active cephalosporin Antibiotic and a prodrug of Cefetamet (HY-A0111). After ingestion, Cefetamet pivoxyl hydrochloride is hydrolyzed by gastrointestinal esterases to form Cefetamet. Cefetamet pivoxyl hydrochloride is primarily active against aerobic Gram-negative bacteria (such as Enterobacteriaceae, Neisseria, Haemophilus) and some Gram-positive bacteria (such as non-enterococcal streptococci). Cefetamet pivoxyl hydrochloride exhibits potent in vivo antibacterial activity against strains of Gram-positive bacteria (S. pyogenes) and Gram-negative bacteria (E. coli, K. pneumoniae, S. marcescens, P. vulgaris, P. mirabilis, H. influenzae) .
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Cat. No.: HY-B1894R
CAS No.: 65243-33-6
Synonyms: Ro 15-8075 free base (Standard)
Cefetamet pivoxyl (Standard) (Ro 15-8075 (free base) (Standard)) is the analytical standard of Cefetamet pivoxyl (HY-B1894). This product is intended for research and analytical applications. Cefetamet pivoxyl (Ro 15-8075 free base) is an orally active cephalosporin Antibiotic and a prodrug of Cefetamet (HY-A0111). After ingestion, Cefetamet pivoxyl is hydrolyzed by gastrointestinal esterases to form Cefetamet. Cefetamet pivoxyl is primarily active against aerobic Gram-negative bacteria (such as Enterobacteriaceae, Neisseria, Haemophilus) and some Gram-positive bacteria (such as non-enterococcal streptococci). Cefetamet pivoxyl exhibits potent in vivo antibacterial activity against strains of Gram-positive bacteria (S. pyogenes) and Gram-negative bacteria (E. coli, K. pneumoniae, S. marcescens, P. vulgaris, P. mirabilis, H. influenzae) .
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Cat. No.: HY-187837
CAS No.: 1426216-93-4
Synonyms: OPS-2071
Abimufloxacin (OPS-2071) is a broad-spectrum quinolone antibacterial agent. Abimufloxacin inhibits the supercoiling activity of DNA gyrase, the decatenation activity of topoisomerase IV, the activation and proliferation of T cells, macrophage activity, as well as the production of TNF-α and IFN-γ. Abimufloxacin exhibits activity against enteropathogenic Gram-positive bacteria, Gram-negative bacteria, quinolone-resistant bacteria, and Crohn's disease-associated bacteria (including Clostridioides difficile and Campylobacter jejuni). Abimufloxacin alleviates colonic inflammation in a mouse model of T cell-mediated colitis. Abimufloxacin can be used in research related to diseases such as intestinal infections and Crohn's disease .
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Cat. No.: HY-B0396B
CAS No.: 1381788-20-0
Synonyms: L084 hydrobromide
Target:  

Antibiotic Bacterial OAT

Research Areas:  

Infection

Tebipenem pivoxil hydrobromide (L084 hydrobromide) is an orally active carbapenem Antibiotic. Tebipenem pivoxil hydrobromide acts as a substrate of OATP1A2 with high affinity for this transporter (Km = 41.1 μM) . Tebipenem pivoxil hydrobromide achieves intestinal absorption via carrier-mediated uptake and simple diffusion. Tebipenem pivoxil hydrobromide inhibits the growth of Gram-positive bacteria, Gram-negative bacteria, multidrug-resistant bacteria, and pathogens producing extended-spectrum β-lactamases. Tebipenem pivoxil hydrobromide eliminates intestinal infection pathogens and reduces mortality in septic mice. Tebipenem pivoxil hydrobromide can be used in research related to bacterial pneumonia, severe gastrointestinal infections, bacterial sepsis, complicated urinary tract infections, and acute pyelonephritis .
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Cat. No.: HY-184868
CAS No.: 18903-23-6
Target:  

Bacterial Herbicide

Research Areas:  

Infection

NSC116565 is an Antibacterial agent, Herbicide, and competitive Ketol-acid reductoisomerase inhibitor, with a Ki of 95.4 nM against Mycobacterium tuberculosis MtKARI. NSC116565 inhibits the growth of mycobacteria by disrupting the branched-chain amino acid biosynthesis pathway, and also inhibits the growth of weeds and brassicas. NSC116565 can be used in tuberculosis-related research .
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