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  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. Nombre del producto Efecto Pureza Chemical Structure
  • HY-B1597R
    Cetalkonium chloride (Standard)
    		Inhibitor
    Cetalkonium (chloride) (Standard) is the analytical standard of Cetalkonium (chloride). This product is intended for research and analytical applications. Cetalkonium chloride is an ammonium antiseptic agent used in many topical agents for infections of mouth, throat and eye. Cetalkonium chloride acts as anti-inflammatory amphiphilic agent. Cetalkonium chloride is a cationic surfactant, that improves the precorneal residence time and bioavailability of drugs. Cetalkonium chloride interacts with the negative charges on the bacterial cell membrane, disrupts the integrity of the cell membrane, causes leakage of cell contents and ultimately leading to bacterial death.
    Cetalkonium chloride (Standard)
  • HY-W108862
    3,3'-Methylenebis[5-methyloxazolidine]
    		Inhibitor
    3,3'-Methylenebis[5-methyloxazolidine] is a bisoxazolidine-based hydrogen sulfide scavenger and fungicide derived from monoisopropanolamine (MIPA). 3,3'-Methylenebis[5-methyloxazolidine] exists as a mixture of structural isomers. 3,3'-Methylenebis[5-methyloxazolidine] is oil-soluble and serves as an oil-soluble alternative to hydrated hexahydrotriazine-based scavengers. 3,3'-Methylenebis[5-methyloxazolidine] can scavenge hydrogen sulfide and methanethiol via chemical reactions, and its scavenging efficiency increases after hydrolysis to MIPA-triazine in water.
    3,3'-Methylenebis[5-methyloxazolidine]
  • HY-178971
    Antimycobacterial agent-13
    		Inhibitor
    Antimycobacterial agent-13 (Compound 3) is an anti tuberculosis agent. Antimycobacterial agent-13 has good antibacterial activity against Mycobacterium tuberculosis (MIC = 3.125 µg/mL) in vitro. Antimycobacterial agent-13 can be used in the research of tuberculosis.
    Antimycobacterial agent-13
  • HY-N14720
    Demethylolivomycin A
    		Inhibitor
    Demethylolivomycin A is an antitumor antibiotic. Demethylolivomycin A has anti-Gram-positive bacteria and anti-leukemia P388 activity.
    Demethylolivomycin A
  • HY-138797
    Griseolutein B
    		Inhibitor
    Griseolutein B shows activitiy against Gram-positive and negative bacteria.
    Griseolutein B
  • HY-159960
    Carbonic anhydrase inhibitor 28
    		Inhibitor
    Carbonic anhydrase inhibitor 28 (Compound 11) is a Pseudomonas aeruginosa carbonic anhydrase inhibitor. Carbonic anhydrase inhibitor 28 exhibits antimicrobial activity, with a MIC of 0.5 μg/mL and a MBC of 1 μg/mL against P. aeruginosa. Carbonic anhydrase inhibitor 28 can be used in anti-infection research.
    Carbonic anhydrase inhibitor 28
  • HY-15597R
    Salinomycin (Standard)
    		Inhibitor
    Salinomycin (Standard) is the analytical standard of Salinomycin. This product is intended for research and analytical applications. Salinomycin (Procoxacin), a polyether potassium ionophore antibiotic, selectively inhibits the growth of gram-positive bacteria. Salinomycin is a potent inhibitor of Wnt/β-catenin signaling, blocks Wnt-induced LRP6 phosphorylation. Salinomycin shows selective activity against human cancer stem cells[1][2][3].
    Salinomycin (Standard)
  • 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-W237019
    3-Ethoxybenzamide
    		Inhibitor
    3-Ethoxybenzamide is an alkoxybenzamide compound with antibacterial activity and a FtsZ inhibitor that can cross the blood-brain barrier. 3-Ethoxybenzamide distributes widely and rapidly in vivo, rapidly reaches equilibrium between various tissues and blood, and is linearly taken up by hepatocytes. 3-Ethoxybenzamide is completely dependent on hepatic microsomal oxidation for clearance, with salicylamide as its major metabolite. 3-Ethoxybenzamide can be used for the study of bacterial infections.
    3-Ethoxybenzamide
  • 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
Cat. No. Nombre del producto / Synonyms Application Reactivity