Antibacterial
Antibacterial inhibitors are compounds that target bacterial cells, inhibiting their growth or killing them outright. These inhibitors are essential in the development of treatments for bacterial infections and are widely used in research to study bacterial physiology, resistance mechanisms, and the efficacy of new antibacterial agents. At CymitQuimica, we offer a range of antibacterial inhibitors to support your research in microbiology, infectious diseases, and drug development.
Found 3318 products for "Antibacterial".
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CHEMBL1276927
CAS:CHEMBL1276927 (N-(3-(1H-benzo[d]imidazol-2-yl)phenyl)-3-methylbenzamide) shows antibacterial and antiparasitic activities against Chlamydia pneumoniae andFormula:C21H17N3OPurity:99.86%Color and Shape:White SolidMolecular weight:327.38SYNV-cyclo(CGGYF) TFA
SYNV-cyclo(CGGYF) TFA: a S. hominis autoinducer that inhibits S. aureus, may help research into S. aureus-related damage.Formula:C48H59F3N10O15SColor and Shape:SolidMolecular weight:1105.1Temporin A acetate
Temporin A acetate is a natural short α-helical antimicrobial peptide against Gram-positive bacteria and fungi.Formula:C70H121N17O16Purity:99.96%Color and Shape:White SolidMolecular weight:1456.84Cefoperazone dihydrate
CAS:Cefoperazone dihydrate, a semi-synthetic cephalosporin, exhibits a wide range of antibacterial properties.Formula:C25H27N9O8S2Color and Shape:SolidMolecular weight:645.67Voxvoganan trihydrochloride
Voxvoganan (LTX-109) trihydrochloride, a topical antimicrobial, demonstrates a high efficacy against S.Formula:C43H72Cl3N11O3Color and Shape:SolidMolecular weight:897.46Urease-IN-21
Urease-IN-21 (Compound 11b) is a urease inhibitor with an IC50 of 0.12 μM. It exhibits potent antibacterial activity against Helicobacter pylori (H. pylori) and inhibits P450 enzymes (CYP2C19, CYP2C9, and CYP3A4). Urease-IN-21 is applicable in research related to H. pylori infections.Color and Shape:Odour SolidVineomycin A1
CAS:Vineomycin A1 (OS-4742 A1) is an antibiotic effective against Gram-positive bacteria, identified in *Streptomyces matensis* subsp. vineus. It has also demonstrated antitumor activity in mice and holds potential for research in skin fibrosis.Formula:C49H58O18Color and Shape:SolidMolecular weight:934.974SPR206
SPR206 is a polymyxin analogue and an important class of antibiotic for the treatment of bacterial infections due to multidrug resistant Gram-negative pathogen.Formula:C52H82ClN15O12Purity:98%Color and Shape:SolidMolecular weight:1144.75Anti-MRSA agent 9
Anti-MRSA agent 9 (compound 39) exhibits antibacterial activity against methicillin-resistant Staphylococcus aureus (MRSA) isolated from clinical samples, with a minimum inhibitory concentration (MIC) of 1 μg/ml. Additionally, Anti-MRSA agent 9 demonstrates anti-MRSA efficacy in vivo.Formula:C39H44BrCl2N2O6PColor and Shape:SolidMolecular weight:816.149741-Ethylnaphthalene
CAS:1-Ethylnaphthalene exhibits antibacterial activity and can be used in biochemical experiments and drug synthesis.Formula:C12H12Color and Shape:SolidMolecular weight:156.22Maximin 8
CAS:Maximin 8, an antimicrobial peptide, is identifiable in B. maxima [1].Formula:C122H213N33O35Color and Shape:SolidMolecular weight:2702.2H-Trp-Trp-Trp-OH
CAS:H-Trp-Trp-Trp-OH is a tripeptide composed of tryptophan residues and exhibits antibacterial activity [1].Formula:C33H32N6O4Color and Shape:SolidMolecular weight:576.64Alendronate prodrug-1
Alendronate prodrug-1 (compound 2) is an inhibitor of farnesyl diphosphate synthase (FPPS) and exhibits antiproliferative activity with an IC50 value of 34.0 μM.Formula:C22H31N3O15P2Color and Shape:SolidMolecular weight:639.12304Vitamin K5
CAS:Vitamin K5, a photosensitizer & antimicrobial, inhibits PKM2, PKM1 & PKL, induces apoptosis in colon cells, and preserves food & medicine.Formula:C11H11NOColor and Shape:SolidMolecular weight:173.21Mtb-IN-12
Mtb-IN-12 (Compound 5m) is a dual-target inhibitor that acts on the Mycobacterium tuberculosis enzymes CYP125 with a dissociation constant (KD) of 40 nM and an inhibition constant (KI) of 0.1 μM, and CYP142 with a KD of 160 nM and a KI of 0.05 μM. It effectively inhibits both drug-sensitive and multidrug-resistant strains of the tuberculosis bacterium, with low toxicity to macrophages, making it useful for studying anti-tuberculosis treatments.Color and Shape:Odour SolidAvibactam Tetrabutylammonium
CAS:Avibactam Tetrabutylammonium is a non-β-lactam β-lactamase inhibitor that inhibits TEM-1, P99, and KPC-2 β-lactamases covalent and reversible.Formula:C23H46N4O6SPurity:99.61%Color and Shape:SolidMolecular weight:506.7LL-37 GKE
CAS:LL-37 GKE, an active domain of LL-37, exhibits antibacterial activity and possesses potential for antibiotic applications [1] [2].Formula:C119H202N38O28Color and Shape:SolidMolecular weight:2613.11MBL-IN-4
MBL-IN-4 (compound 4b) is an MBL inhibitor with IC50 values of 4.81 μM for IMP-1 and 33 μM for NDM-1.Formula:C27H36N2O2Color and Shape:SolidMolecular weight:420.27768Retrocyclin-3
CAS:Retrocyclin-3 is an antimicrobial peptide that exhibits activity against human immunodeficiency virus (HIV), influenza A, and herpes simplex virus (HSV) [1].Formula:C82H146N36O18S6Color and Shape:SolidMolecular weight:2116.66Ethambutol-D10
CAS:Ethambutol-D10 is the deuterated form of Ethambutol. Ethambutol (T7062) acts as an antimycobacterial agent by inhibiting the activity of arabinosyl transferase, thereby preventing the formation of the bacterial cell wall.Formula:C10H24N2O2Color and Shape:SolidMolecular weight:214.37
