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

Bacterial

Bacterial

Related Products

PDF 14.26 MB

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-W714837
    5-Phenyllevulinic acid
    		Inhibitor
    5-Phenyllevulinic acid (4-Oxo-5-phenylpentanoic acid) is an endogenous fungal metabolite with inhibitory activity against the bacterium B. megaterium, the plant pathogenic fungus S. tritici, and the alga C. fusca. 5-Phenyllevulinic acid is also an intermediate in the synthesis of σ receptor ligands. 5-Phenyllevulinic acid holds potential for research in the field of anti-infection studies .
    5-Phenyllevulinic acid
  • HY-N14711
    Himalomycin A
    		Inhibitor
    Himalomycin A is an anthraquinone antibiotic with strong activity against Staphylococcus aureus, Escherichia coli and Streptomyces vuridochromogenes.
    Himalomycin A
  • HY-121245
    Capoamycin
    		Inhibitor
    Capoamycin is an antibiotic. Capoamycin shows antimicrobial and antitumor activity.
    Capoamycin
  • HY-N9492
    (+)-2-Carene
    		Control
    4497-92-1
    (+)-2-Carene
  • HY-N14545
    Oxamicetin
    		Inhibitor
    Oxamicetin is a nucleoside antibiotic. Oxamicetin has anti-bacterial, mycobacterium effects.
    Oxamicetin
  • HY-N14946
    5-Deoxygentamicin C1
    		Inhibitor
    5-Deoxygentamicin C1 has anti-Gram-positive and anti-Gram-negative activities.
    5-Deoxygentamicin C1
  • HY-B0455R
    Lomefloxacin hydrochloride (Standard)
    		Inhibitor
    Lomefloxacin (hydrochloride) (Standard) is the analytical standard of Lomefloxacin hydrochloride (HY-B0455). This product is intended for research and analytical applications. Lomefloxacin hydrochloride (NY-198 hydrochloride) is an orally active difluoroquinolone antibiotic. Lomefloxacin hydrochloride prevents DNA supercoiling and replication by inhibiting bacterial topoisomerase II. Lomefloxacin hydrochloride induces ROS production and Apoptosis. Lomefloxacin hydrochloride has broad-spectrum bactericidal activity against Gram-positive and Gram-negative bacteria. Lomefloxacin hydrochloride has anticancer effects against melanoma. Lomefloxacin hydrochloride can be used in the study of systemic bacterial infections (such as Salmonella typhimurium infections), skin and melanoma .
    Lomefloxacin hydrochloride (Standard)
  • HY-P1708
    Enopeptin A
    Enopeptin A, originally isolated from a culture broth of Streptomyces sp. RK-1051, is a depsipeptide antibiotic that contains two unusual amino acids (N-methylalanine and 4-methylproline) and features a pentaenone side chain. It is effective against Gram-positive bacteria, including methicillin-resistant S. aureus (MIC=25 μg/mL), and Gram-negative bacteria, including mutant forms of E. coli and P. aeruginosa (MICs=200 μg/mL); however, it is not inhibitory to fungi.
    Enopeptin A
  • HY-N13150
    Norvancomycin
    		Inhibitor
    N-Demethylvancomycin is a glycopeptide antibiotic which can be extracted from Nocardia orientalis and active against several strains of S. aureus and S. epidermidis. N-Demethylvancomycin can be used for infection research.
    Norvancomycin
  • HY-N15359
    Germicidin C
    		Inhibitor
    Germicidin C is a microbial metabolite with antibacterial activity, which is found in the marine sponge-derived fungus Aspergillus niger. Germicidin C can inhibit the growth of various pathogenic bacteria such as Staphylococcus aureus, Escherichia coli, and Bacillus subtilis with MIC values ranging from 32 to 64 µg/mL.
    Germicidin C
  • HY-N14080
    Monamycin G2
    		Inhibitor
    Monamycin G2 is an ester peptide antibiotic. Monamycin G2 has activity against Gram-positive bacteria.
    Monamycin G2
  • HY-144071
    MurB-IN-1
    MurB-IN-1 is an inhibitor of Pseudomonas aeruginosa UDP-N-acetylmuramic acid enolpyruvyl reductase (MurB) with a Kd value of 3.57 μM. MurB-IN-1 is applicable to the research of Pseudomonas aeruginosa infections (cystic fibrosis-associated).
    MurB-IN-1
  • HY-B0458AS
    Cefprozil-d4
    		Inhibitor
    Cefprozil-d4 is the deuterium labeled Cefprozi (HY-B0458A). Cefprozil is a second-generation cephalosporin type antibiotic. Cefprozil exhibits broad-spectrum antibacterial activity, and is orally active. Cefprozil can be used for the study of pharyngitis, tonsillitis, otitis media, and uncomplicated skin infections.
    Cefprozil-d<sub>4</sub>
  • HY-121474
    Dactimicin
    		Inhibitor
    Dactimicin is a pseudodisaccharide aminoglycoside. Dactimicin is an antibiotic that can inhibit the growth of methicillin-susceptible S. aureus isolates and coagulase-negative staphylococci with MIC50s of 2 μg/mL. Dactimicin is active against organisms possessing aminoglycoside-modifying enzymes.
    Dactimicin
  • HY-181820
    Topoisomerase IV-IN-3
    		Inhibitor
    Topoisomerase IV-IN-3 is a Staphylococcus aureus Topoisomerase IV inhibitor, DNA gyrase inhibitor and antibacterial agent. Topoisomerase IV-IN-3 has IC50 values of 1.32 μM and 0.48 μM against topoisomerase IV, and 0.88 μM and 0.54 μM against DNA gyrase. Topoisomerase IV-IN-3 inhibits decatenation, ATPase, and supercoiling activities of its target enzymes. Topoisomerase IV-IN-3 exerts antibacterial activity against Gram-positive and Gram-negative bacterial strains. Topoisomerase IV-IN-3 exhibits low cytotoxicity toward human fibroblast cells. Topoisomerase IV-IN-3 can be used for the research of bacterial infections.
    Topoisomerase IV-IN-3
  • HY-113532
    Isofusidienol A
    		Inhibitor
    Isofusidienol A (Compound 26) is a chromone compound. Isofusidienol A can be isolated from Artemisia vulgaris. Isofusidienol A has significant antibacterial activity against Bacillus subtilis. Isofusidienol A also has potent antifungal activity against Candida albicans. Isofusidienol A can be used for bacterial and fungal infections research.
    Isofusidienol A
  • HY-137748A
    3′-MANT-2′d-ATP tetrasodium
    		Modulator
    3′-MANT-2′d-ATP (3′-MANT-2′deoxy-ATP ) tetrasodium is an inhibitor of edema factor. 3′-MANT-2′d-ATP tetrasodium inhibits the catalytic activity of EF3.
    3′-MANT-2′d-ATP tetrasodium
  • HY-Y0585R
    D-(-)-Mandelic acid (Standard)
    		Inhibitor
    D-(-)-Mandelic acid (Standard) is the analytical standard of D-(-)-Mandelic acid. This product is intended for research and analytical applications. D-(-)-Mandelic acid is an orally active alpha hydroxycarboxylic acid that can be isolated from bitter almonds and Indian chestnut trees. It has antioxidant and antibacterial properties and is expected to play an important role in the treatment of rheumatoid arthritis.
    D-(-)-Mandelic acid (Standard)
  • HY-N15055
    Propeptin
    		Inhibitor
    Propeptin is a peptide antibiotic composed of 19 amino acids. Propeptin has weaker activity against Pseudomonas aeruginosa, Mycobacterium monobacterium, and Xanthomonas oryzae. Propeptin has no effect on KB and L1210 cells of tumor cell lines, but has an inhibitory effect on prolyl endopeptidase.
    Propeptin
  • HY-133060
    Sannamycin B
    		Inhibitor
    Sannamycin B is an aminoglycoside antibiotic. Sannamycin B has only weak antibacterial activity against a few bacteria.
    Sannamycin B
Cat. No. Product Name / Synonyms Application Reactivity