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-113590
    FR295389
    Inhibitor
    FR295389 is a dihydroimidazopyrazolium cephalosporin with antibacterial activity. FR295389 shows activity against IMP-type metallo-β-lactamases (MBL)-producing Klebsiella pneumoniae, Acinetobacter baumanii and Pseudomonas putida with MIC values ranging from 4 to 32 mg/mL.
    FR295389
  • HY-B1046R
    Clofazimine (Standard)
    Inhibitor
    Clofazimine (Standard) is the analytical standard of Clofazimine. This product is intended for research and analytical applications. Clofazimine is an orally-active anti-mycobacterial agent with a wide range of anti-mycobacterial activity including leprosy and tuberculosis. Clofazimine exerts anti-inflammatory activities and anti-tumor activities by interfering DNA replication and inhibiting IL2 (IC50 = 1.10 ± 0.26 μM, Jurkat T) production. Clofazimine can be used in mycobacterial and cancer research.
    Clofazimine (Standard)
  • HY-N14519
    Pacidamycin 7
    Inhibitor
    Pacidamycin 7 has inhibitory effect on Pseudomonas aeruginosa. Pacidamycin 7 also has effect on a few strains of bacteria such as suppurative staphylococcus and Escherichia coli. Serum can reduce its antibacterial activity, pH also affects its antibacterial activity.
    Pacidamycin 7
  • HY-N14708
    Kibdelin C1
    Inhibitor
    Kibdelin C1 is resistant to Gram-positive bacteria and has similar effects against Staphylococcus aureus (including methicillin-resistant strains) as Vancomycin (HY-B0671).
    Kibdelin C1
  • HY-N15026
    13-Hydroxyglucopiericidin A
    Inhibitor
    13-Hydroxyglucopiericidin A is an antibiotic. 13-Hydroxyglucopiericidin A has strong anti-tumor cell activity.
    13-Hydroxyglucopiericidin A
  • HY-N1181R
    Tamarixetin (Standard)
    Inhibitor
    Tamarixetin (Standard) is the analytical standard of Tamarixetin. This product is intended for research and analytical applications. Tamarixetin (4'-O-Methyl Quercetin) is an orally active natural flavonoid derivative of quercetin and caseinolytic protease p (ClpP) inhibitor with anti-inflammatory, antioxidant and antitumor effects. Tamarixetin inhibits the hydrolytic activity of ClpP to the fluorescent substrate Suc-LY-AMC with an IC50 of 49.73 μM, which can be used for the study of Staphylococcus aureus infection. Tamarixetin inhibits tumor cell growth, induces apoptosis, and cell cycle arrest. Tamarixetin prevents cardiac hypertrophy by inhibiting the NFAT and AKT pathways.
    Tamarixetin (Standard)
  • HY-N5200
    4"-Demethylgentamicin C1a
    Inhibitor
    4"-Demethylgentamicin C1a has anti-Gram-positive and negative bacteria activity.
    4
  • HY-W000800R
    cis,cis-Muconic acid (Standard)
    cis,cis-Muconic acid (Standard) is an analytical standard for cis,cis-Muconic acid (HY-W000800). This product is used for research and analytical applications. cis,cis-Muconic acid is a dicarboxylic acid produced by Saccharomyces cerevisiae. cis,cis-Muconic acid shows pH-dependent toxicity against Saccharomyces cerevisiae CEN.PK113-7D. cis,cis-Muconic acid can be used as intermediate for the production of various plastics and polymers.
    cis,cis-Muconic acid (Standard)
  • HY-N14912
    β-Prumycin hydrochloride
    Inhibitor
    β-Prumycin hydrochloride is a carbohydrate antibiotic. β-Prumycin hydrochloride has anti-fungal activity and weak anti-individual bacterial activity.
    β-Prumycin hydrochloride
  • HY-N15353
    1-Palmitoyl-2-linoleoyl-sn-glycerol
    1-Palmitoyl-2-linoleoyl-sn-glycerol is a diacylglycerol (DAG)-type lipid signaling molecule found in the coralloid roots of Cycas revoluta, and serves as a major active component of the plant-secreted hormogonium-inducing factor (HIF). At a concentration of 1 nmol/disc (approximately 0.6 µg), 1-palmitoyl-2-linoleoyl-sn-glycerol can significantly induce the differentiation of filamentous aggregates of Nostoc into motile hormogonia, thereby promoting chemotaxis toward host roots and the establishment of symbiosis. This compound holds significant research and application potential in areas such as plant–microbe interactions, rhizosphere signaling pathways, and nitrogen-fixing symbiosis.
    1-Palmitoyl-2-linoleoyl-sn-glycerol
  • HY-15025S3
    Sildenafil-d5
    Sildenafil-d5 (UK-92480-d5) is deuterium labeled Sildenafil. Sildenafil (UK-92480) is a potent phosphodiesterase type 5 (PDE5) inhibitor with an IC50 of 5.22 nM.
    Sildenafil-d<sub>5</sub>
  • HY-119771
    Schizokinen
    Schizokinen is an iron-transport agent. Schizokinen can be obtained from Bacillus megaterium. Schizokinen possesses a higher affinity for iron(III) than Desferrioxamine B. Schizokinen reduces the division lag of bacteria.
    Schizokinen
  • HY-175596
    ACP1-01
    Inhibitor
    ACP1-01 is a bacterial ClpP activator with EC50s of 3.4 and 2.6  μM for Neisseria meningitides ClpP (NmClpP) and Escherichia coli ClpP (EcClpP). ACP1-01 noncovalently binds to ClpP C sites and activates the protease. ACP1-01 has antibacterial activity. ACP1-01 can be used for bacterial infections research.
    ACP1-01
  • HY-N14529
    Oganomycin B
    Inhibitor
    Oganomycin B is more stable than cephalosporin and resistant to Gram-positive and negative bacteria. And it is more effective against Gram-negative bacteria than Gram-positive bacteria.
    Oganomycin B
  • HY-N15019
    Glycothiohexide α
    Inhibitor
    Glycothiohexide α is a peptide antibiotic. Glycothiohexide α has strong activity against Gram-positive bacteria including methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin resistant enterococcus (VREF), MIC values of 0.03-0.06 μg/mL.
    Glycothiohexide α
  • HY-138870
    Enzyme-IN-3 disodium
    Inhibitor
    Enzyme-IN-3 disodium (compound 7) is a selective inhibitor of Mycobacterium tuberculosis shikimate kinase with an IC50 of 1.6 μM. Enzyme-IN-3 disodium has antibacterial activity.
    Enzyme-IN-3 disodium
  • HY-B0656S1
    Rabeprazole-13C,d3
    Rabeprazole-13C,d3 is a deuterated labeled Rabeprazole. Rabeprazole (LY307640) is a second-generation proton pump inhibitor (PPI) that irreversibly inactivates gastric H+/K+-ATPase. Rabeprazole induces apoptosis. Rabeprazole acts as an uridine nucleoside ribohydrolase (UNH) inhibitor with an IC50 of 0.3 μM. Rabeprazole can be used for the research of gastric ulcerations and gastroesophageal reflux.
    Rabeprazole-<sup>13</sup>C,d<sub>3</sub>
  • HY-106852A
    KP 736 sodium
    Inhibitor
    KP 736 sodium is a broad-spectrum antibacterial agent. KP 736 sodium exhibits excellent broad-spectrum anti Gram negative bacterial activity in vitro, especially effective against Pseudomonas aeruginosa and multiple drug-resistant bacteria. KP 736 sodium can be used for research on bacterial infections.
    KP 736 sodium
  • HY-N14835
    Formadicin C
    Inhibitor
    Formadicin C has the strongest activity against some pseudomonas, Proteus and alkali producing bacilli.
    Formadicin C
  • HY-105180
    Lenapenem
    Inhibitor
    Lenapenem (BO-2727 free acid), a carbapenem antibiotic, has potent antibacterial activity against Gram-positive and Gram-negative bacteria including P. aeruginosa.
    Lenapenem
Cat. No. Product Name / Synonyms Application Reactivity