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-N5127R
    Nonacosane (Standard)
    Inhibitor
    Nonacosane (Standard) is the analytical standard of Nonacosane. This product is intended for research and analytical applications. Nonacosane, isolated from Baphia massaiensis, exhibits weak activities against E. coli, B. subtilis, P. aeruginosa and S. aureus.
    Nonacosane (Standard)
  • HY-N14397
    8"-Hydroxypactamycin
    Inhibitor
    8''-Hydroxypactamycin is an antibiotic found in Streptomyces SIPI-A-3-0121.
    8
  • HY-N13287
    Ayapin
    Inhibitor
    Ayapin is a major phytoalexin found in sunflower. Ayapin inhibits the growth of S. scerorotiorum (IC50 of 0.16 mM for 50% inhibition). Ayapin can be used in anti-sclerotinia research.
    Ayapin
  • HY-N14906
    4-Diazo-3-methoxy-2,5-cyclohexadien-1-one
    Inhibitor
    4-Diazo-3-methoxy-2,5-cyclohexadien-1-one has favourable anti-anaerobe activity. MIC: 0.4 μg/mL for Clostridium and Bacterioids, 0.2 μg/mL for Haemophilus.
    4-Diazo-3-methoxy-2,5-cyclohexadien-1-one
  • HY-P5551
    TLN-58
    Inhibitor
    TLN-58 is an antimicrobial peptide. TLN-58 has antibacterial activity against S. aureus, S. epidermidis, and group A Streptococcus. TLN-58 also induces inflammatory cytokine mRNAs upregulation in normal human keratinocytes and NCL-SG3 cells.
    TLN-58
  • HY-N14503
    Mycinamicin Ⅳ
    Inhibitor
    Monamycin IV is an ester peptide antibiotic. Monamycin IV has activity against Gram-positive bacteria.
    Mycinamicin Ⅳ
  • HY-N0916
    Monomelittoside
    Inhibitor
    Monomelittoside is a iridoid glycoside with antibacterial activity. Monomelittoside inhibits dental caries pathogen Streptococcus.
    Monomelittoside
  • HY-186108
    ZY38
    Inhibitor
    ZY38 is a SaClpP agonist that activates SaClpP-mediated α-casein hydrolysis with an EC50 of 1.52 μM. ZY38 exhibits bactericidal activity against Staphylococcus aureus. ZY38 is applicable to studies related to Staphylococcus aureus infections, such as peritonitis.
    ZY38
  • HY-116558
    E-4441
    Inhibitor
    E-4441 is an orally active Antibacterial agent. E-4441 exerts broad-spectrum in vitro antibacterial activity against Gram-positive bacteria and aerobic bacteria. E-4441 exhibits protective effects against Staphylococcus aureus, Escherichia coli, and Pseudomonas aeruginosa infections. E-4441 can be used in the research of systemic bacterial infections (Staphylococcus aureus, Escherichia coli, and Pseudomonas aeruginosa infections).
    E-4441
  • HY-W740764
    Isopropyl 4-hydroxybenzoate-d7
    Inhibitor
    Isopropyl 4-hydroxybenzoate-d7 is the deuterium labeled Isopropyl 4-hydroxybenzoate (HY-W016491). Isopropyl 4-hydroxybenzoate (Isopropylparaben) is an antimicrobial and antioxidant agent.
    Isopropyl 4-hydroxybenzoate-d<sub>7</sub>
  • HY-B0944R
    Pidotimod (Standard)
    Inhibitor
    Pidotimod (Standard) is the analytical standard of Pidotimod. This product is intended for research and analytical applications. Pidotimod is an orally active dipeptide immunostimulant with immunomodulatory properties on the adaptive and the innate immune responses. Pidotimod increases macrophage activity and humoral immune functions. Pidotimod can be used for the research of chronic bronchitis, chronic obstructive pulmonary disease (COPD), bronchiectasis, and chronic idiopathic urticaria,et al.
    Pidotimod (Standard)
  • HY-17025S1
    Rifabutin-d6
    Inhibitor
    Rifabutin-d6 (Ansamycin-d6) is deuterium labeled Rifabutin. Rifabutin (Ansamycin) is a semisynthetic ansamycin antibiotic with potent antimycobacterial properties. Rifabutin inhibits DNA-dependent RNA polymerase.
    Rifabutin-d<sub>6</sub>
  • HY-W928623
    2-Acetylthiophene thiosemicarbazone
    Inhibitor
    2-Acetylthiophene thiosemicarbazone is an antibacterial agent. 2-Acetylthiophene thiosemicarbazone exhibits anticancer activity, with an IC50 value of 8.6 μM against HT-29 cells.
    2-Acetylthiophene thiosemicarbazone
  • HY-118234
    (Rac)-PD 138312
    Inhibitor
    (Rac)-PD 138312 is the racemate of PD 138312. PD 138312 is a potent and orally active antibacterial agent against Gram-positive bacteria.
    (Rac)-PD 138312
  • HY-N8519
    Urdamycin B
    Inhibitor
    Urdamycin B is an antibiotic that effectively inhibits fungi and bacteria. Urdamycin B also exhibits anti-proliferative activity against mouse leukemia cells L1210. Urdamycin B can be obtained from the metabolic products of Streptomyces fradiae. Urdamycin B can be used for research on cancer as well as bacterial and fungal infections.
    Urdamycin B
  • HY-W028039
    4,4-Dimethyloxazolidine
    Inhibitor
    4,4-Dimethyloxazolidine is an antimicrobial agent used in industrial processing chemicals and specialty industrial products to inhibit the growth of bacterial and fungal.
    4,4-Dimethyloxazolidine
  • HY-W741062
    15-Methylhexadeca Sphinganine
    Inhibitor
    Sphinganine (d16:0 branched) is an iso-branched sphingolipid. It has been found as a component of ceramide-containing phospholipids in bacteria.
    15-Methylhexadeca Sphinganine
  • HY-N14090
    Chrysospermin C
    Inhibitor
    Chrysospermin C has antibacterial activities against individual Gram-positive bacteria (Staphylococcus aureus, Bacillus subtilis), Klebsiella pneumoniae and individual yeasts (Ocher echinoderma, saccharomyces cerevisiae).
    Chrysospermin C
  • HY-B1190S2
    Cefadroxil-13C6
    Inhibitor
    Cefadroxil-13C6 (BL-S 578-13C6) is 13C labeled Cefadroxil (HY-B1190). Cefadroxil is an orally active broad-spectrum cephalosporin antibiotic. Cefadroxil inhibits bacterial cell wall synthesis and enhances the expression of glutamate transporter-1. Cefadroxil is dependent on the intestinal peptide transporter PepT1 for small intestinal absorption. Cefadroxil has inhibitory and bactericidal activity against a variety of Gram-positive and Gram-negative bacteria and has analgesic effects on neuropathic pain.
    Cefadroxil-<sup>13</sup>C<sub>6</sub>
  • HY-19071
    BK-218
    Inhibitor
    BK-218 is an orally active cephalosporin antibiotic that binds to penicillin-binding proteins (PBPs) and has a greater inhibitory effect than Cephalexin (HY-B0200) and Cefoxitin (HY-B1825). BK-218 has similar antibacterial activity to Cefamandole (HY-B1128) and can be used in the development of antibacterial drugs.
    BK-218
Cat. No. Product Name / Synonyms Application Reactivity