Bacterial compound (inhibitors, antagonists)-ProbeChem.com

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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-28495	Kasugamycin hydrochloride Antibiotic	Kasugamycin hydrochloride (Ksg) is a small ribosomal subunit-targeting antibiotic, binds to the bacterial 30S ribosomal subunit and inhibits canonical translation initiation, possesses anti-infective activity.
PC-28494	Kasugamycin Antibiotic	Kasugamycin (Ksg) is a small ribosomal subunit-targeting antibiotic, binds to the bacterial 30S ribosomal subunit and inhibits canonical translation initiation, possesses anti-infective activity.
PC-28393	NDM-552 PBP2 inhibitor	NDM-552 is a Gram-positive selective antibacterial agent that potentially targets penicillin-binding protein 2 (PBP2)-associated cell wall biosynthesis, exhibits activity against Gram-positive pathogens including S. aureus, Enterococcus faecium, and Staphylococcus epidermidis with MIC of 1-2 ug/mL.
PC-28263	Murepavadin TFA Antibiotic, MRGPRX2 agonist	Murepavadin TFA (POL7080) is a highly potent, specific, macrocycle Pseudomonas antibiotic, activates mast cells via MRGPRX2 and MrgprB2.
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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