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Request The Product List ofBacterial Bacterial

Bacteria constitute a large domain of prokaryoticmicroorganisms. Antibiotics (also called antibacterials) are a type of antimicrobial drug used in the treatment and prevention of bacterial infections, a limited number of antibiotics also possess antiprotozoal activity. Together with vaccination, antibiotics have led to the near eradication of diseases such as tuberculosis in the developed world. However, their effectiveness and easy access have also led to their overuse, prompting bacteria to develop resistance.

A bactericidal activity of antibacterials may depend on the bacterial growth phase, and it often requires ongoing metabolic activity and division of bacterial cells. In vitro characterization of antibacterial activity commonly includes the determination of the minimum inhibitory concentration and minimum bactericidal concentration of an antibacterial. To predict clinical outcome, the antimicrobial activity of an antibacterial is usually combined with its pharmacokinetic profile, and several pharmacological parameters are used as markers of drug efficacy.

 
 

Cat. No. Product Name Information
PC-24403

HilD inhibitor C26

S. Typhimurium HilD inhibitor

HilD inhibitor C26 is a specific small molecule inhibitor of  S. Typhimurium transcriptional regulator HilD with IC50 of 16.9 uM and binds to HilD with an apparent Kd of 30.2 uM, inhibits the secretion of SipA with IC50 of 29.2 uM.
PC-24393

FG-2101

LpxC inhibitor

FG-2101 (FG2101) is a potent, in vivo active, non-hydroxamate inhibitor of LpxC with IC50 of 1 nM, exhibits exquisite selectivity over other bacterial and human metalloenzymes (>10,000-fold).
PC-24388

MBX-4132

Trans-translation inhibitor

MBX-4132 is a trans-translation inhibitor with IC50 of 0.6 uM and 0.4 uM in E. coli luciferase reporter assay and in vitro reconstituted assays respectively, exhibits potent broad-spectrum antibiotic activity against Gram-positive species and many Gram-negative species.
PC-24353

H052

S. aureus α-hemolysin inhibitor

H052 is a highly potent S. aureus α-hemolysin (Hla) inhibitor, protect U937 cells from Hla-induced Ca2+ influx with EC50 of 0.01 uM, restores Hla-induced damage of host cell integrity.
PC-24346

NCBP1

Antibacterial

NCBP1 is a plant-derived, 11 amino acid, noncanonical antibacterial peptide with dual activity against multidrug-resistant bacterial and fungal pathogens, by targeting phosphatidylglycerol and cardiolipin in bacterial membrane, resulting in membrane damage and dysfunction.
PC-24340

DNA gyrase inhibitor 35

2088347-91-3

DNA gyrase inhibitor 35 is potent small molecule DNA gyrase inhibitor with IC50 of 1.2 μM of E.coli DNA gyrase, also shows low micromolar inhibition of E. coli topoisomerase IV and of the respective Staphylococcus aureus homologues.
PC-24339

Astrazeneca Arylaminotriazine

DNA gyrase inhibitor

Astrazeneca Arylaminotriazine is a promising DNA gyrase inhibitor with profound antibacterial activity.
PC-24338

10-F05

FabH/MiaA inhibitor

10-F05 is a covalent small molecule inhibitor of bacterial β-ketoacyl-acyl carrier protein synthase III (FabH) and MiaA tRNA prenyltransferase, demonstrates broad-spectrum antibacterial effectiveness (MIC=2.5 uM, S. flexneri).
PC-24315

Lariocidin

Antibiotic

Lariocidin (LAR) is a novel ribosome-targeting lasso peptide antibiotic inhibit bacterial growth by binding to the ribosome and interfering with protein synthesis.
PC-24305

P2-56-3

Rifampin potentiator

P2-56-3 is small-molecule sensitizer of antibiotic-resistant gram-negative ESKAPE pathogens, potentiates rifampin against antibiotic-resistant strains of Acinetobacter baumannii and Klebsiella pneumoniae, disrupts the outer membrane of A. baumannii.
PC-24304

Rifampin

Antibiotic

Rifampin (Rifampicin) is a potent and broad spectrum antibiotic against bacterial pathogens, also has anti-influenza virus and anti-orthopoxvirus activities.
PC-24301

Fosfomycin sodium

Antibiotic

Fosfomycin (MK-0955) sodium is a blood-brain barrier penetrating, broad-spectrum antibiotic by irreversibly inhibiting an early stage in cell wall synthesis, shows a wide range antibacterial activity, including multidrug-resistant (MDR), extensively drug-resistant (XDR), and pan-drug-resistant (PDR) bacteria.

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