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

Bacterial

Bacterial

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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-W983893
    7-Hydroxytropolone
    		Inhibitor
    7-Hydroxytropolone (3-Hydroxytropolone) is an antibiotic with anti-Gram-positive bacteria, negative bacteria, yeast and fungi activity, and has the effect of inhibiting 2''-O-Adenylyltransferase.
    7-Hydroxytropolone
  • HY-N14752
    Hydroxymycotrienin A
    		Inhibitor
    Hydroxymycotrienin A is an Ansa antibiotic. Hydroxymycotrienin A has the activity of inhibiting human neck tumor cell line, and its inhibitory effect on human papillomavirus (HPV) gene positive neck tumor cells (such as HeLa, CaSKi, SiHa, etc.) is stronger than HPV gene negative cells.
    Hydroxymycotrienin A
  • HY-129804
    Ceforanide (lysine)
    		Inhibitor
    Ceforanide lysine is a second generation cephalosporin administered intravenously or intramuscularly. Ceforanide lysine has a spectrum of in vitro antibacterial activity.
    Ceforanide (lysine)
  • HY-N11778
    Bequinostatin C
    Bequinostatin C is a naphthoquinone originally isolated from Streptomyces and a glutathione S-transferase pi 1 (GSTP1) inhibitor (IC50=40 μg/mL for human GSTP1).
    Bequinostatin C
  • HY-N14782
    10-Decarbomethoxyaclacinomycin A
    		Inhibitor
    10-Decarbomethoxyaclacinomycin A is an anthracycline antibiotic can be produced by Streptomyces galilaeus MA144-Mlt mutant strain KE303. 10-Decarbomethoxyaclacinomycin A has antibacterial activities.
    10-Decarbomethoxyaclacinomycin A
  • HY-117566
    RPR 102341
    RPR 102341 is structurally similar to the fluoroquinolone class of antibiotics.
    RPR 102341
  • HY-W769714
    Favipiravir-13C3
    		Inhibitor
    Favipiravir-13C3 is the 13C labeled isotope of Favipiravir-13C3(HY-14768 ).Favipiravir (T-705) is a potent viral RNA polymerase inhibitor, it is phosphoribosylated by cellular enzymes to its active form, Favipiravir-ribofuranosyl-5′-triphosphate (RTP). Favipiravir-RTP inhibits the influenza viral RNA-dependent RNA polymerase (RdRP) activity with an IC50 of 341 nM.
    Favipiravir-<sup>13</sup>C<sub>3</sub>
  • HY-N14338
    Sannamycin L
    		Inhibitor
    Sannamycin L is an aminoglycoside antibiotic. Sannamycin L has weak antibacterial activity against Gram-positive bacteria and Gram-negative bacteria.
    Sannamycin L
  • HY-N6715R
    Tenuazonic acid (Standard)
    		Inhibitor
    Tenuazonic acid (Standard) is the analytical standard of Tenuazonic acid. This product is intended for research and analytical applications. Tenuazonic acid is a nonhost-selective mycotoxin belonging to the tetramic acids family. Tenuazonic acid inhibits protein biosynthesis on ribosomes by suppressing the release of new protein. Tenuazonic acid is acutely toxic, and oral LD50 is set between 81-186 mg/kg in rats and mice. Tenuazonic acid blocks electron transport beyond the primary quinone receptor (QA) by interacting with the D1 protein and is a photosystem II (PSII) inhibitor. In addition, Tenuazonic acid has antiviral effects on measles virus, enterovirus, respiratory virus and so on. Tenuazonic acid has an inhibitory effect on skin cancer.
    Tenuazonic acid (Standard)
  • HY-N14786
    2-Hydroxy-5-iminoazacyclopent-3-ene
    		Inhibitor
    2-Hydroxy-5-iminoazacyclopent-3-ene is a pyrroline antibiotic. 2-Hydroxy-5-iminoazacyclopent-3-ene has weak anti-Gram-positive and negative bacteria activity.
    2-Hydroxy-5-iminoazacyclopent-3-ene
  • HY-173219
    SrtA-IN-1
    		Inhibitor
    SrtA-IN-1 (Compound T10) is an inhibitor of Streptococcus pyogenes sortase A (SpSrtA), with an IC50 value of 0.7 μM. SrtA-IN-1 can be used in the research of the anti-infection field.
    SrtA-IN-1
  • HY-A0088S
    Cefotaxime-d3 sodium
    		Inhibitor
    Cefotaxime-d3 (sodium) is the deuterium labeled Cefotaxime (sodium salt). Cefotaxime sodium salt, a β-lactamase stable cephalosporin and a third-generation cephalosporin antibiotic, possesses broad-spectrum antibiotic activity against numerous Gram-positive and Gram-negative bacteria.
    Cefotaxime-d<sub>3</sub> sodium
  • HY-N13947
    Pyralomicin 1b
    		Inhibitor
    Pyralomicin 1b is an antibiotic with antibacterial activity.
    Pyralomicin 1b
  • HY-N14866
    Monorden B
    		Inhibitor
    Monorden B has the effect of arresting the cell cycle of Jurket cells in G1 and G2/M phases. Monorden B has anti-Aspergillus niger activity.
    Monorden B
  • HY-W130307R
    Tricosane (Standard)
    		Inhibitor
    Tricosane (Standard) (N-Tricosane (Standard)) is the analytical standard of Tricosane (HY-W130307). This product is intended for research and analytical applications. Tricosane (N-Tricosane) is a straight-chain alkane. Tricosane exhibits a certain degree of antibacterial activity against E. coli.
    Tricosane (Standard)
  • HY-W854341
    Chitotriose
    Chitotriose is a chitooligosaccharide that can be isolated from crab shell chitosan. Chitotriose has antibacterial effect against salmonella.
    Chitotriose
  • HY-N14302
    44-Homooligomycin A
    		Inhibitor
    44-HomooIigomycin A is an antitumor antibiotic. 44-Homooligomycin A has activity against fungi such as Aspergillus, Penicillium and Fusarium, but not against yeast and bacteria. 44-Homooligomycin A has moderate anti-tumor activity against Colon 26 in vivo.
    44-Homooligomycin A
  • HY-B0306R
    Prothionamide (Standard)
    		Inhibitor
    Prothionamide (Standard) is the analytical standard of Prothionamide (HY-B0306). This product is intended for research and analytical applications. Prothionamide is an orally active thioamide antibacterial agent. Prothionamide is a substrate of OCT1 with a Km value of 805.8 μM. Prothionamide reacts with NAD to form a covalent adduct, with the adduct being a tight-binding inhibitor of Mycobacterium tuberculosis and Mycobacterium leprae InhA. Prothionamide can effectively inhibit the growth of Mycobacterium tuberculosis (MIC = ~0.5 µg/mL) and Mycobacterium leprae. Prothionamide is used in the research of tuberculosis and leprosy.
    Prothionamide (Standard)
  • HY-N14150
    Darlucin A
    		Inhibitor
    Darlucin A has antibacterial and fungi activity, and weak cytotoxicity.
    Darlucin A
  • HY-129234
    Mazethramycin
    		Inhibitor
    Mazethramycin is an antitumor antibiotic that exerts its antitumor effect by interfering with cellular DNA replication and RNA synthesis. Mazethramycin can be used in cancer research.
    Mazethramycin
Cat. No. Product Name / Synonyms Application Reactivity