2. Signaling Pathways
  3. Anti-infection
  4. Bacterial

Bacterial

Bacterial

Related Products

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Anything that destroys bacteria or suppresses their growth or their ability to reproduce. Heat, chemicals such as chlorine, and antibiotic drugs all have antibacterial properties. Many antibacterial products for cleaning and handwashing are sold today. Such products do not reduce the risk for symptoms of viral infectious diseases in otherwise healthy persons. This does not preclude the potential contribution of antibacterial products to reducing symptoms of bacterial diseases in the home.

Cat. No. Product Name Effect Purity Chemical Structure
  • HY-N14168
    Ashimycin A
    		Inhibitor
    Ashimycin A is a Streptomycin (HY-B1906) analogue with a broad-spectrum antibacterial activity.
    Ashimycin A
  • HY-B1781S
    Sulfachloropyridazine-13C6
    		Inhibitor
    Sulfachloropyridazine-13C6 is the 13C6 labeled Sulfachloropyridazine. Sulfachloropyridazine is a broad spectrum sulfonamide used against both Gram-positive and Gram-negative aerobic bacteria.
    Sulfachloropyridazine-<sup>13</sup>C<sub>6</sub>
  • HY-B0330S1
    (S)-Ofloxacin-d3
    		Inhibitor 98.0%
    (S)-Ofloxacin-d3 is the deuterium labeled Levofloxacin. Levofloxacin, a synthetic fluoroquinolone, is an antibacterial agent that inhibits the supercoiling activity of bacterial DNA gyrase, halting DNA replication.
    (S)-Ofloxacin-d<sub>3</sub>
  • HY-174263
    PaFabV-IN-1
    		Inhibitor
    PaFabV-IN-1 (Compound 3e) is a selective Pseudomonas aeruginosa enoyl-acyl carrier protein reductase (PaFabV) inhibitor with an IC50 value of 0.25 μM. PaFabV-IN-1 is promising for research of infections caused by P. aeruginosa and other Gram-negative bacteria.
    PaFabV-IN-1
  • HY-184237
    Antibacterial agent 349
    		Inhibitor
    Antibacterial agent 349 is an antibacterial agent. Antibacterial agent 349 impairs reactive oxygen species clearance, disrupts citrate cycle homeostasis and induces metabolic stress. Antibacterial agent 349 compromises bacterial membrane integrity, increases permeability, and causes intracellular component leakage. Antibacterial agent 349 can be used for the research of bacterial leaf streak.
    Antibacterial agent 349
  • HY-W016969R
    2-Undecanone (Standard)
    		Inhibitor
    2-Undecanone (Standard) is the analytical standard of 2-Undecanone (HY-W016969). This product is intended for research and analytical applications. 2-Undecanone is an orally active organic ketone. 2-Undecanone exerts antibacterial effects by inhibiting bacterial chaperone systems and interfering with the refolding of heat-inactivated proteins. 2-Undecanone also ameliorates asthmatic inflammation and airway remodeling by blocking the NF-κB pathway, and activates the Nrf2 pathway to reduce oxidative damage and prevent lung cancer induced by Benzo[a]pyrene (HY-107377). 2-Undecanone can be used in research related to cancer, asthma and infections.
    2-Undecanone (Standard)
  • HY-139654
    α/β-Hydrolase-IN-1
    		Inhibitor
    α/β-Hydrolase-IN-1 exhibits the best-in-class MICs of 50 μM (25 μg/mL) and 16 μM (8.4 μg/mL) against M. smegmatis and M. tuberculosis H37Ra, respectively.
    α/β-Hydrolase-IN-1
  • HY-19421
    Orazamide
    		Inhibitor
    Orazamide is an AICA orotate. Orazamide can prevent anti-TB drug-induced liver damage by downregulating the protein expression of HMGB 1 and RAGE in liver tissue and inhibiting the secretion of inflammatory factors. Orazamide can be used in research on hepatitis and liver cirrhosis.
    Orazamide
  • HY-B0526R
    Flumequine (Standard)
    		Inhibitor
    Flumequine (Standard) is the analytical standard of Flumequine. This product is intended for research and analytical applications. Flumequine (R-802) is a quinolone antibiotic, and acts as a topoisomerase II inhibitor, with an IC50 of 15 μM (3.92 μg/mL).
    Flumequine (Standard)
  • HY-101048
    Synthalin A sulfate
    		Inhibitor
    Synthalin A sulfate is a biguanylated diamine with antibacterial and hypoglycemic properties. Synthalin A sulfate against S. aureus with a MIC of 64 μg/mL.
    Synthalin A sulfate
  • HY-17507CS
    (R)-(+)-Pantoprazole-d6
    (R)-(+)-Pantoprazole-d6 is deuterium labeled (R)-(+)-Pantoprazole.
    (R)-(+)-Pantoprazole-d<sub>6</sub>
  • HY-W794609
    Pinocarveol
    		Inhibitor 98.38%
    Pinocarveol is a monoterpene found in Pistacia atlantica subsp. kurdica hulls’ essential oil. Pinocarveol exhibits antioxidant and antibacterial activities.
    Pinocarveol
  • HY-P5547
    Lynronne-3
    		Inhibitor
    Lynronne-3 is an antimicrobial peptide. Lynronne-1 is active against Gram-positive bacterials, including MDR strains (MIC: 32-128 μg/mL for methicillin-resistant MRSA strains). Lynronne-3 is also effective against P. aeruginosa infection
    Lynronne-3
  • HY-123315
    Sulfaperin
    		Inhibitor 99.87%
    Sulfaperin (Methylsulfadiazin) is an antibacterial agent.
    Sulfaperin
  • HY-N16461
    Albomycin ε
    		Control
    Albomycin ε is a siderophore-antibiotic conjugate targeting bacterial ribosomes (MIC values:>512 μg/mL). Albomycin ε is promising for research of Streptococcus pneumoniae and Staphylococcus aureus infections.
    Albomycin ε
  • HY-158141
    BRD1401
    		Inhibitor
    BRD1401 is a small molecule targeting the outer membrane protein OprH. BRD1401 disrupts the interaction of OprH with LPS. BRD1401 can increase membrane fluidity.
    BRD1401
  • HY-B1466R
    Mezlocillin sodium (Standard)
    		Inhibitor
    Mezlocillin (sodium) (Standard) is the analytical standard of Mezlocillin (sodium). This product is intended for research and analytical applications. Mezlocillin (BAY-f 1353) sodium is a β-lactam antibiotic, a semisynthetic and extended-spectrum antibiotic. Mezlocillin sodium is active against both gram-negative and gram-positive bacteria. Mezlocillin sodium can be used in bacterial infection research[1][2].
    Mezlocillin sodium (Standard)
  • HY-138671
    DprE1-IN-4
    		Inhibitor
    DprE1-IN-4 is a potent and orally active noncovalent DprE1 inhibitor with an IC50 of 0.90 μg/mL. DprE1-IN-4 exhibits potent in vitro activity against M. tuberculosis H37Rv and drug-resistant tuberculosis strain with MIC values of 0.12 μg/mL and 0.24 μg/mL, respectively. DprE1-IN-4 displays acceptable pharmacokinetic property and shows significant bactericidal activity in an acute mouse model of tuberculosis.
    DprE1-IN-4
  • HY-183340
    Antibacterial agent 341
    Antibacterial agent 341 is an anti-bacterial agent. Antibacterial agent 341 shows broad-spectrum Gram-positive antibacterial activity. Antibacterial agent 341 targets phosphatidylglycerol (PG) and cardiolipin (CL) in bacterial cell membranes, induces sustained depolarization of membranes, and disrupts the cell membrane integrity. Antibacterial agent 341 exhibits anti-infection activity against S. aureus-induced subcutaneous abscesses in mice.
    Antibacterial agent 341
  • HY-N6681
    15-Acetoxyscirpenol
    		Inhibitor 99.35%
    15-acetoxyscirpenol, one of acetoxyscirpenol moiety mycotoxins (ASMs), strongly induces apoptosis and inhibits Jurkat T cell growth in a dose-dependent manner by activating other caspases independent of caspase-3.
    15-Acetoxyscirpenol
Cat. No. Product Name / Synonyms Application Reactivity