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

Bacterial

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-B0268S2
    Enoxacin-d8 hydrate
    Inhibitor
    Enoxacin-d8 (hydrate) is deuterium labeled Enoxacin. Enoxacin (AT 2266), a fluoroquinolone, interferes with DNA replication and inhibits bacterial DNA gyrase (IC50=126 μg/ml) and topoisomerase IV (IC50=26.5 μg/ml). Enoxacin is a miRNA processing activator and enhances siRNA-mediated mRNA degradation and promotes the biogenesis of endogenous miRNAs. Enoxacin has potent activities against gram-positive and -negative bacteria. Enoxacin is a cancer-specific growth inhibitor that acts by enhancing TAR RNA-binding protein 2 (TRBP)-mediated microRNA processing.
    Enoxacin-d<sub>8</sub> hydrate
  • HY-B0334S
    Sulbactam-d3
    Inhibitor
    Sulbactam-d3 (CP45899-d3) is deuterium labeled Sulbactam. Sulbactam (CP45899) is a competitive, irreversible beta-lactamase inhibitor. Sulbactam shows antimicrobial activity against multidrug-resistant (MDR) acinetobacter calcoaceticus--Acinetobacter baumannii (Acb) complex.
    Sulbactam-d<sub>3</sub>
  • HY-17358R
    Loteprednol Etabonate (Standard)
    Inhibitor
    Loteprednol Etabonate (Standard) is the analytical standard of Loteprednol Etabonate. This product is intended for research and analytical applications. Loteprednol etabonate (LE) is an orally active "soft" steroid belonging to a unique class of glucocorticoids. Loteprednol etabonate (LE) exhibits anti-inflammatory activity and has been used in optometry and ophthalmology.
    Loteprednol Etabonate (Standard)
  • HY-B0512A
    Sulfamerazine sodium salt
    Inhibitor
    Sulfamerazine Sodium is a sulfonamide antibacterial.
    Sulfamerazine sodium salt
  • HY-N14484
    Kigamicin D
    Inhibitor
    Kigamicin D shows activity against Gram-positive bacteria including methicillin-resistant Staphylococcus aureus (MRSA) with MICs of 0.025-0.78 μg/mL. Kigamicin D also shows effect against L-1210 LB32T and other genera tumor cells with IC50 of 1 μg/mL.
    Kigamicin D
  • HY-178800
    Antibacterial agent 296
    Inhibitor
    Antibacterial agent 296 (Compound Q24) is an antibacterial agent. Antibacterial agent 296 inhibits biofilm formation, reduces extracellular polysaccharides. Antibacterial agent 296 shows inhibitory activity against Xanthomonas axonopodis pv. citri (Xac), with an EC50 of 5.13 μg/mL.
    Antibacterial agent 296
  • HY-N13986
    Seldomycin factor 5
    Inhibitor
    Seldomycin factor 5 (XK 88-5) is an aminoglycoside antibiotic. Seldomycin factor 5 has a broad spectrum of antimicrobial activity.
    Seldomycin factor 5
  • HY-N2512R
    1-Monomyristin (Standard)
    Inhibitor
    1-Monomyristin, extracted from Serenoa repens, inhibits the hydrolysis of 2-oleoylglycerol (IC50=32 μM) and fatty acid amide hydrolase (FAAH) activity (IC50=18 μM). 1-Monomyristin shows antibacterial activity against Staphylococcus aureus and Aggregatibacter actinomycetemcomitans and also antifungal activity against Candida albicans.
    1-Monomyristin (Standard)
  • HY-N14457
    Platenomycin W2
    Inhibitor
    Platenomycin W2 is a macrolide antibiotic with anti-Gram-positive bacteria activities.
    Platenomycin W2
  • HY-121173
    1-Aminoacridine
    Inhibitor
    1-Aminoacridine (1-Acridinamine) is a bright fluorescent dye. 1-Aminoacridine acts as an anti-infective agent and mutagen due to its ability to interact with DNA.
    1-Aminoacridine
  • HY-B0771AR
    Cefozopran hydrochloride (Standard)
    Inhibitor
    Cefozopran (hydrochloride) (Standard) is the analytical standard of Cefozopran (hydrochloride). This product is intended for research and analytical applications. Cefozopran (SCE-2787) hydrochloride is a semi-synthetic, parenteral, fourth-generation cephalosporin. Cefozopran hydrochloride, an antibiotic, has a broad spectrum of antibacterial activity, inhibiting most of the gram-negative and gram-positive organisms.
    Cefozopran hydrochloride (Standard)
  • HY-N0827
    Perillene
    Inhibitor
    Perillene is a component of the essential oil, has antibacterial and antitumor effects.
    Perillene
  • HY-122030
    Lithooxazoline
    Inhibitor
    Lithooxazoline is a potent antibacterial agent.
    Lithooxazoline
  • HY-173205
    Antimycobacterial agent-11
    Inhibitor
    Antimycobacterial agent - 11 (Compound QM7) is a bacteriostatic agent with anti-tuberculosis activity. Its minimum inhibitory concentration (MIC) against Mycobacterium tuberculosis (Mtb) is 5.58 μg/mL. Antimycobacterial agent - 11 can be used in the research of the anti - infection field, especially in the field of tuberculosis.
    Antimycobacterial agent-11
  • HY-B0732AS
    Itopride-d6
    Itopride-d6 (HSR803-d6 (free base)) is deuterium labeled Itopride. Itopride (HSR803 free base) is a potent and orally active dopamine-2 antagonist and an acetylcholine esterase (AChE) inhibitor. Itopride enhances gastric motility through both antidopaminergic and anti-acetylcholinesterasic actions, can be used as a gastrointestinal prokinetic agent. Itopride can be used for researching gastro-esophageal reflux disease (GERD).
    Itopride-d<sub>6</sub>
  • HY-16672
    AVX 13616
    Inhibitor
    AVX 13616 shows the potent in vivo antibacterial activity of Avexa’s lead antibacterial candidate; particularly against drug-resistant Staphylococcus pathogens.
    AVX 13616
  • HY-B0545S1
    Probenecid-d7
    Inhibitor
    Probenecid-d7 is deuterium-labeled Probenecid (HY-B0545).
    Probenecid-d<sub>7</sub>
  • HY-N14709
    Kibdelin C2
    Inhibitor
    Kibdelin C2 is resistant to Gram-positive bacteria and has similar effects against Staphylococcus aureus (including methicillin-resistant strains) as Vancomycin (HY-B0671).
    Kibdelin C2
  • HY-168061
    HldA/E-IN-1
    Inhibitor
    HldA/E-IN-1 (compound 8) is a dual inhibitor of HldA/E, with IC50 values ​​of 17.2 μM and 67.8 μM for HldA/E, respectively. HldA/E-IN-1 can be used in the study of anti-bacterial infection.
    HldA/E-IN-1
  • HY-10581R
    Gatifloxacin (Standard)
    Inhibitor
    Gatifloxacin (Standard) is the analytical standard of Gatifloxacin. This product is intended for research and analytical applications. Gatifloxacin (AM-1155; BMS-206584; PD135432) is a potent fluoroquinolone antibiotic with broad-spectrum antibacterial activity. Gatifloxacin inhibits bacterial type II topoisomerases (IC50=13.8 μg/ml for S. aureus topoisomerase IV) and E. coli DNA gyrase (IC50=0.109 μg/ml). Gatifloxacin can be used to treat bacterial conjunctivitis in vivo.
    Gatifloxacin (Standard)
Cat. No. Product Name / Synonyms Application Reactivity