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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-27136

SmcR inhibitor PTSP

SmcR inhibitor

PTSP is a specific and potent inhibitor of Vibrio LuxR/HapR proteins and LuxR homolog SmcR in Vibrio vulnificus, inhibits quorum sensing in multiple strains of V. vulnificus, V. parahaemolyticus, and V. campbellii.
PC-27134

ZN148

Metallo-β-lactamase inhibitor

ZN148 (APC148) is a specific, irreversible, zinc-chelating metallo-β-lactamase (MBL) inhibitor with broad activity against Ambler class B enzymes, including NDM, VIM, and IMP, restores the in vitro and in vivo activity of meropenem against multidrug-resistant MBL-producing Enterobacterales.
PC-27116

Cap5-IN-1

Bacterial Cap5 inhibitor

Cap5-IN-1 is a competitive, cellulo active inhibitor of bacterial cyclic oligonucleotide-based anti-phage signaling system (CBASS) effector nuclease Cap5, effectively blocks phage defenses in bacteria.
PC-27101

MP20

N. gonorrhoeae inhibitor

MP20 is a small molecule antibiotic effective against Neisseria gonorrhoeae with MIC of 4 ug/mL for N. gonorrhoeae ATCC 49226, shows in vitro efficacy against multidrug-resistant N. gonorrhoeae strains
PC-27035

Linezolid

Antibacterial

Linezolid (PNU-100766) is an oxazolidone antibiotic for staphylococcal and streptococcal infections, also has certain activity against gram-negative bacteria and anaerobes, also is a selective inhibitor of JAK2 V617F mutation but not with wild-type JAK2 protein.
PC-26865

AIP-II

AgrC inhibitor

AIP-II is a peptidomimetic inhibitor of staphylococcus aureus AgrC quorum sensing receptors, inhibits AgrC-III in methicillin-resistant type III Staphylococcus aureus strain AH1747 with IC50 of 0.532 nM, binds to the AgrC-II receptor and regulates virulence gene expression in Staphylococcus aureus.
PC-26828

MRL-494 hydrochloride

BamA inhibitor

MRL-494 hydrochloride (MRL494) is an antimicrobial small molecule that inhibits assembly of outer membrane proteins (OMPs) by the β-barrel assembly machine (BAM complex), inhibits the insertion of OMPs into the OM by targeting BamA.
PC-26808

BRD1554

Mtb Pks13 inhibitor

BRD1554 is a selective inhibitor of Mycobacterium tuberculosis polyketide synthase 13 (Pks13).
PC-26780

Fluorothiazinone

T3SS inhibitor, Anti-virulence

Fluorothiazinone is a small molecule antivirulent compound that suppresses the formation of biofilms, inhibits the type III secretion system (T3SS) in Gram-negative bacteria.
PC-26720

KGDI-109

PgDPP7 inhibitor

KGDI-109 is the first substrate-mimetic dipeptide inhibitor of P. gingivalis dipeptidyl peptidase 7 (PgDPP7) with IC50 of 53.8 uM and Ki of 25.1 uM, exerts an inhibitory effect against P. gingivalis growth with MIC of 1.56 uM.
PC-26708

BDM91531

AcrB efflux pump inhibitor

BDM91531 is a potent AcrB efflux pump inhibitor, binds to the TMD of the L state and O state protomers of AcrB, exhibits potent potentiation of pyridomycin activity with EC90 of 0.24 uM.
PC-26671

Funobactam

β-lactamase inhibitor

Funobactam (XNW4107) is a novel β-lactamase inhibitor that possesses broad activity against serine-β-lactamases, displays in vitro activity against Ambler class A, C, and D β-lactamases.

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