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-186107
    ZY36
    		Inhibitor
    ZY36 is a SaClpP agonist with an EC50 of 1.01 μM against Staphylococcus aureus. ZY36 activates SaClpP-mediated proteolysis. ZY36 inhibits the growth of Staphylococcus aureus. ZY36 is applicable to studies related to Staphylococcus aureus infections, such as peritonitis.
    ZY36
  • HY-122174
    ME-1036
    		Inhibitor
    ME-1036 (CP-5609) is a carbapenem antibiotic. ME-1036 against resistant Gram-positive organisms, including Methicillin-resistant Staphylococcus aureus (MRSA), and vancomycin-resistant Enterococci (VRE), and ESBL-producing E. coli and K. pneumoniae but is not effective against P. aeruginosa.
    ME-1036
  • HY-P5720
    Peptide 5e
    		Inhibitor
    Peptide 5e is an antimicrobial peptide. Peptide 5e inhibits E. coli, S. aureus, and C. albicans with MIC values of 30, 5, 25 μg/mL respectively.
    Peptide 5e
  • HY-N12149
    Axinysone B
    		Inhibitor
    Axinysone B can be isolated from Laurencia similis. Axinysone B has antibacterial activity against Staphylococcus sp..
    Axinysone B
  • HY-N14042
    Arizonin B2
    		Inhibitor
    Arizonin B2 is a microbial metabolite with anti-Gram-positive bacterial activities.
    Arizonin B2
  • HY-W654567
    N,N-Dimethyl-N-(3-(trimethoxysilyl)propyl)tetradecan-1-aminium chloride
    		Inhibitor
    N,N-Dimethyl-N-(3-(trimethoxysilyl)propyl)tetradecan-1-aminium chloride is a cationic surfactant of the silylated quaternary ammonium salt type, possessing dual functions of antibacterial activity and silane coupling. N,N-Dimethyl-N-(3-(trimethoxysilyl)propyl)tetradecan-1-aminium chloride can be used as a cationic silane coupling agent, antibacterial surface treatment agent, and disinfectant.
    N,N-Dimethyl-N-(3-(trimethoxysilyl)propyl)tetradecan-1-aminium chloride
  • HY-182684
    MMV675968
    		Inhibitor
    MMV675968 is an inhibitor of Acinetobacter baumannii dihydrofolate reductase (AbDHFR) with an IC50 of 8.5 nM, and it exhibits selectivity against human DHFR. MMV675968 inhibits dihydrofolate reductase in Cryptosporidium, Plasmodium, and Escherichia coli, disrupting the thymidylate cycle and folate biosynthesis pathway. MMV675968 inhibits the growth of multiple A. baumannii strains, including clinical isolates and environmental isolates. MMV675968 is applicable to research related to A. baumannii infections.
    MMV675968
  • HY-N14819
    Defucogilvocarcin V
    		Inhibitor
    Defucogilvocarcin V is a gilvocarcin antibiotic with activity against Gram-positive bacteria.
    Defucogilvocarcin V
  • HY-163107
    Antimycobacterial agent-7
    		Inhibitor
    Antimycobacterial agent-7 (compound 4) is a 1,2,4-triazole anti-tuberculosis agent (MIC: 2 μg/mL). Antimycobacterial agent-7 inhibits Mtb KatG and causes the accumulation of ROS in Mtb cells. ROS produces oxidative damage, leading to the death of Mtb.
    Antimycobacterial agent-7
  • HY-185308
    Trisaccharides 3
    		Inhibitor
    Trisaccharides 3 (compoudn 3) is a GlfT2 acceptor substrate with a 50 μM Ka. Trisaccharides 3 acts as an acceptor substrate for the β-(1→6) galactofuranosyl transferase activity of GlfT2, binds competitively at GlfT2’s single active site pocket, and undergoes galactosylation by GlfT2 with UDP-Galf to form a tetrasaccharide product. Trisaccharides 3 can be used for the research of tuberculosis, hiv-associated Mycobacterium avium infections.
    Trisaccharides 3
  • HY-157142
    Antibacterial agent 165
    		Inhibitor
    Antibacterial agent 165 (compound 3), a hydroxyquinoline derivative, is a potent bacterial inhibitor. Antibacterial agent 165 inhibits methicillin-resistant Staphylococcus aureus (MRSA).
    Antibacterial agent 165
  • HY-W014316R
    5-Bromo-5-nitro-1,3-dioxane (Standard)
    		Inhibitor
    5-Bromo-5-nitro-1,3-dioxane (Standard) is the analytical standard of 5-Bromo-5-nitro-1,3-dioxane (HY-W014316). This product is intended for research and analytical applications. 5-Bromo-5-nitro-1,3-dioxane is a broad-spectrum antimicrobial agent active against Gram-positive bacteria, Gram-negative bacteria and fungi. 5-Bromo-5-nitro-1,3-dioxane oxidizes free thiol groups to their corresponding disulfides. 5-Bromo-5-nitro-1,3-dioxane induces intracellular substance leakage in Escherichia coli and Staphylococcus aureus. 5-Bromo-5-nitro-1,3-dioxane modulates the oxygen consumption of Escherichia coli and Staphylococcus aureus.
    5-Bromo-5-nitro-1,3-dioxane (Standard)
  • HY-W811579
    Bensuldazic acid
    		Inhibitor
    Bensuldazic acid (compound 4f) is a lipophilic 3,5-disubstituted tetrahydro-2H-1,3,5-thiadiazine-2-thione (THTT) derivative that can be used as a prodrug model. Bensuldazic acid has antifungal activity.
    Bensuldazic acid
  • HY-B0644R
    Sucralfate (Standard)
    		Inhibitor
    Sucralfate (Standard) is the analytical standard of Sucralfate. This product is intended for research and analytical applications. Sucralfate (Sucrose octasulfate-aluminum complex) is a potent and orally active gastroprotectant with no systemic effects. Sucralfate inhibits peptic activity and binds to negatively charged subepithelial proteins exposed during mucosal injury, forming a viscous layer that protects the vascular bed and proliferative zone. Sucralfate is used for prevention and research of several gastrointestinal diseases in vivo.
    Sucralfate (Standard)
  • HY-169811
    CPW-86-363
    		Inhibitor
    CPW-86-363 is a novel broad-spectrum cephalosporin with antibacterial activity.
    CPW-86-363
  • HY-N14731
    7-Demethylpiericidin A1
    		Inhibitor
    7-Demethylpiericidin A1 is a pierceridin antibiotic. 7-Demethylpiericidin A1 has antifungal and Gram-negative bacteria activity.
    7-Demethylpiericidin A1
  • HY-116611
    IMB-YH-8
    		Inhibitor
    IMB-YH-8 is a serine/threonine protein kinase (PknB) inhibitor. IMB-YH-8 has strong antibacterial activity against Mycobacterium tuberculosis (MIC = 0.25 µg/mL). IMB-YH-8 can be used in the research of tuberculosis.
    IMB-YH-8
  • HY-W108875R
    Mupirocin lithium (Standard)
    		Inhibitor
    Mupirocin (lithium) (Standard) is the analytical standard of Mupirocin lithium (HY-W108875). This product is intended for research and analytical applications. Mupirocin lithium is an antibiotic. Mupirocin lithium inhibits bacterial isoleucyl-tRNA synthetase, blocking protein synthesis. Mupirocin lithium has high activity against Gram-positive bacteria such as Staphylococcus and Streptococcus, as well as some Gram-negative bacteria (such as Haemophilus influenzae). Mupirocin lithium can be used in the research of diseases such as skin infections (such as MRSA infections) and chronic sinusitis.
    Mupirocin lithium (Standard)
  • HY-N14613
    Rhodomycin B
    		Inhibitor
    Rhodomycin B has the activity of anti-Gram-positive bacteria and weak effect on anti-Gram-negative bacteria and fungi.
    Rhodomycin B
  • HY-N13905
    Alliacol A
    		Inhibitor
    Alliacol A is an antibiotic shows weak antibacterial and antifungal activity. Alliacol A inhibits DNA synthesis in cells of the ascitic form of Ehrlich carcinoma.
    Alliacol A
Cat. No. Product Name / Synonyms Application Reactivity