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-163625
    Mtb-IN-7
    		Inhibitor
    Mtb-IN-7 (compoun R7) is a MAO-A/MAO-B inhibitor with the IC50 values over 40 μM. Mtb-IN-7 shows antimycobacterial activity against M. tuberculosis H37Rv with the MIC of 2.01 μM.
    Mtb-IN-7
  • HY-N14481
    Phenelfamycin B
    		Inhibitor
    Phenelfamycins B is an antibiotic with anti-eutrophic bacterial activity.
    Phenelfamycin B
  • HY-N15069
    4'-O-Demethyldianemycin
    		Inhibitor
    4'-O-Demethyldianemycin (TM-531B) is a polyether antibiotic found in Streptomyces hygroscopicus TM-531. Activity against Gram-positive bacteria.
    4'-O-Demethyldianemycin
  • HY-116168
    Aldecalmycin
    		Inhibitor
    Aldecalmycin is an antibiotic showing antimicrobial activities against Gram-positive bacteria including methicillin-resistant Staphylococcus aureus (MRSA) with MICs values of 6.25-25 μg/mL.
    Aldecalmycin
  • HY-B1300R
    Cefonicid sodium (Standard)
    		Inhibitor
    Cefonicid (sodium) (Standard) is the analytical standard of Cefonicid (sodium). This product is intended for research and analytical applications. 0
    Cefonicid sodium (Standard)
  • HY-N0683S6
    α-Vitamin E-d11
    		Inhibitor
    α-Vitamin E-d11 ((+)-α-Tocopherol-d11) is the deuterium labeled α-Vitamin E (HY-N0683). α-Vitamin E ((+)-α-Tocopherol), a naturally occurring vitamin E form, is a potent antioxidant.
    α-Vitamin E-d<sub>11</sub>
  • HY-W782391
    Linolenyl alcohol
    		Inhibitor
    Linolenyl alcohol is an unsaturated alcohol that inhibits Gram-positive bacteria.
    Linolenyl alcohol
  • HY-155462
    hERG-IN-1
    		Inhibitor
    hERG-IN-1 (compound 2a) is an antibacterial agent and inhibitor of hERG. hERG-IN-1 inhibits pulmonary infection caused by Pseudomonas aeruginosa strain ATCC 27853.
    hERG-IN-1
  • HY-113619
    ABT-255 free base
    		Inhibitor
    ABT-255 free base is an orally active anti-bacterial agent. ABT-255 free base exhibits potent in vitro potency (MIC = 0.016-0.031 μg/mL) against drug-susceptible and Rifampin (HY-B0272)- or Ethambutol (HY-B0535)-resistant Mycobacterium tuberculosis. ABT-255 free base shows efficacy against S. aureus, S. pneumoniae and E. coli and reduces viable counts of drug-resistant Mycobacterium tuberculosis in CF-1 mice. ABT-255 free base can be used for the study of pulmonary tuberculosis.
    ABT-255 free base
  • HY-129814
    MM 42842 free acid
    		Inhibitor
    MM 42842 free acid is a member of the monobactam family of β-lactam antibiotics.
    MM 42842 free acid
  • HY-B0958R
    Mupirocin (Standard)
    		Inhibitor
    Mupirocin (Standard) is the analytical standard of Mupirocin (HY-B0958). This product is intended for research and analytical applications. Mupirocin is an antibiotic. Mupirocin inhibits bacterial isoleucyl-tRNA synthetase, blocking protein synthesis. Mupirocin has high activity against Gram-positive bacteria such as Staphylococcus and Streptococcus, as well as some Gram-negative bacteria (such as Haemophilus influenzae). Mupirocin can be used in the research of diseases such as skin infections (such as MRSA infections) and chronic sinusitis.
    Mupirocin (Standard)
  • HY-115407
    Cochliodone A
    		Inhibitor
    Cochliodone A is an active compound extracted from cultures of the deep-sea derived fungus Chaetomium sp. and has antibacterial and anticancer activity. Cochliodone A is toxic to a variety of bacteria, with MICs of 15.3 μg/mL (V. vulnificus), 32.7 μg/mL (V. rotiferianus), 15.9 μg/mL (S. aureus ATCC 43300), and 16.3 μg/mL (S . aureus CGMCC 1.12409). Cochliodone A also inhibits a variety of cancer cell lines, with IC50s of 28.1 μM (A549), 20.7 μM (HeLa), and 23.2 μM (Hep G2).
    Cochliodone A
  • HY-17507S2
    Pantoprazole-d8
    Pantoprazole-d8 (BY1023-d8) is deuterium labeled Pantoprazole. Pantoprazole (BY10232) is an orally active and potent proton pump inhibitor (PPI). Pantoprazole, a substituted benzimidazole, is a potent H+/K+-ATPase inhibitor with an IC50 of 6.8 μM. Pantoprazole improves pH stability and has anti-secretory, anti-ulcer activities. Pantoprazole significantly increased tumor growth delay combined with Doxorubicin (HY-15142).
    Pantoprazole-d<sub>8</sub>
  • HY-W097867
    3-Desmethyl Gatifloxacin
    		Inhibitor
    3-Desmethyl Gatifloxacin (8-Methoxy Ciprofloxacin) induces DNA cleavage mediated by wild-type gyrase and Quinolone-resistant mutants. 3-Desmethyl Gatifloxacin can be used for research of drug resistance.
    3-Desmethyl Gatifloxacin
  • HY-122284
    CP-5068
    		Inhibitor
    CP-5068is a cell wall inhibitor that can be used for the study of infectious diseases.
    CP-5068
  • HY-B1174R
    Bekanamycin (Standard)
    		Inhibitor
    Bekanamycin (Standard) is the analytical standard of Bekanamycin. This product is intended for research and analytical applications. Bekanamycin (Kanamycin B) is an aminoglycoside antibiotic produced by Streptomyces kanamyceticus, against an array of Gram-positive and Gram-negative bacterial strain.
    Bekanamycin (Standard)
  • HY-168117
    HP-101
    		Inhibitor
    HP-101 is a cell-permeable dual-substrate inhibitor of HPPK with activity against Gram-positive bacteria..
    HP-101
  • HY-117837
    GSK1829820A
    GSK1829820A has antitubercular activity which can inhibit Mycobacterium tuberculosis H37Rv.
    GSK1829820A
  • HY-170575
    Pks13-IN-1
    		Inhibitor
    Pks13-IN-1 (Compound 44) is an orally active inhibitor for Mycobacterium tuberculosis Polyketide synthase 13 (Pks13). Pks13-IN-1 inhibits M. tuberculosis strain H37Rv with a MIC of 0.07 μM. Pks13-IN-1 exhibits antibacterial efficacy in mouse model.
    Pks13-IN-1
  • HY-N11407
    Bagougeramine B
    		Inhibitor
    Bagougeramine B is an orally active nucleoside antibiotic with antimicrobial activity, which is found in Bacillus circulans. Bagougeramine B inhibits the growth of Gram-positive and Gram-negative bacteria and some fungi.
    Bagougeramine B
Cat. No. Product Name / Synonyms Application Reactivity