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首页-小分子抑制剂&激动剂-Antibiotics and Antivirals-Bacterial

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-45925

Moxifloxacin hydrochloride

Antibiotic, DNA gyrase inhibitor

Moxifloxacin hydrochloride (BAY 12-8039) is a fourth-generation synthetic fluoroquinolone, broad-spectrum antibacterial agent that is active against both Gram-positive and Gram-negative bacteria, inhibits DNA gyrase and topoisomerase IV.
PC-42665

Gatifloxacin

Bacterial DNA gyrase inhibitor

Gatifloxacin (PD 135432, AM1155) is a fourth-generation fluoroquinolone antibiotic that inhibits the bacterial DNA gyrase and topoisomerase IV.
PC-42048

Faropenem daloxate

Beta-lactam antibiotic

Faropenem daloxate (Faropenem medoxil) is a daloxate ester prodrug of Faropenem with broad-spectrum antibacterial activity against many gram-positive and gram-negative aerobes and anaerobes, a beta-lactam antibiotic.
PC-42714

Pretomanid

Mtb inhibitor

Pretomanid (PA-824) is an anti-tuberculosis agent that inhibits the synthesis of protein and cell wall lipid.
PC-28185

MtbIMPDH inhibitor 31

Mtb GuaB inhibitor

MtbIMPDH inhibitor 31 is a potent, specific inhibitor of Mycobacterium tuberculosis inosine 5'-monophosphate dehydrogenase (Mtb GuaB, MtbIMPDH) with IC50 of 0.52 uM.
PC-28184

MtbIMPDH2 inhibitor P41

GuaB2 inhibitor

MtbIMPDH2 inhibitor P41 is a potent, specific inhibitor of Mycobacterium tuberculosis inosine 5'-monophosphate dehydrogenase (Mtb GuaB, MtbIMPDH) with Ki app of 17 nM for MtbIMPDH2ΔCBS, displays significant activity against Mtb strain H37Rv in minimal BSA-free medium with MIC of 5 uM.
PC-28181

Mtb GuaB-IN-2

Mtb GuaB inhibitor

Mtb GuaB-IN-2 is a potent, specific inhibitor of Mycobacterium tuberculosis inosine 5'-monophosphate dehydrogenase (Mtb GuaB, IMPDH) with IC50 of 0.2 nM.
PC-28180

Mtb GuaB-IN-1

Mtb GuaB inhibitor

Mtb GuaB-IN-1 (Compound 15) is a potent, specific inhibitor of Mycobacterium tuberculosis inosine 5'-monophosphate dehydrogenase (Mtb GuaB2, IMPDH) with IC50 of 1.7 nM, and MIC of0.26 uM for M.tb H37Ra.
PC-28120

Sulfamethoxazole

Antibiotic, DHPS inhibitor

Sulfamethoxazole (Ro 4-2130) is a sulfonamide antibiotic for various bacterial, interferes with folic acid synthesis in susceptible bacteria, is a competitive dihydropteroate synthase (DHPS) inhibitor.
PC-27825

TrmD-IN-4

TrmD inhibitor

TrmD-IN-4 is a potent, covalent inhibitor of bacterial tRNA (m1G37) methyltransferase (TrmD) with IC50 of 4.43 uM, with minimal inhibition of human Trm5, shows selective growth inhibition in bacteria expressing TrmD.
PC-27824

TrmD-IN-3

TrmD inhibitor

TrmD-IN-3 is a potent, covalent inhibitor of bacterial tRNA (m1G37) methyltransferase (TrmD) with IC50 of 1.17 uM for E. coli TrmD, with minimal inhibition of human Trm5 (IC50=2.17 mM), shows selective growth inhibition in bacteria expressing TrmD.
PC-27823

TrmD-IN-2

TrmD inhibitor

TrmD-IN-2 is a potent, covalent inhibitor of bacterial tRNA (m1G37) methyltransferase (TrmD) with IC50 of 0.85 uM for E. coli TrmD, with minimal inhibition of human Trm5 (IC50=1.88 mM), shows selective growth inhibition in bacteria expressing TrmD.

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