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-N14237
    Epoxyquinomicin A
    		Inhibitor
    Epoxyquinomicin A is an antibiotic that can be isolated from Amycolatopsis sp. Epoxyquinomicin A exhibits inhibitory activity against Micrococcus luteus, Bacillus subtilis, Pasteurella piscicida and Staphylococcus aureus with a MIC of 3-12.5 µg/mL. Epoxyquinomicin A exhibits cytotoxicity in cancer cell L1210, B16 and S180 with IC50 of 2-8 µg/mL. Epoxyquinomicin A exhibits anti-inflammatory effects against collagen-induced arthritis.
    Epoxyquinomicin A
  • HY-163843
    Antibacterial agent 234
    		Inhibitor
    Antibacterial agent 234 (6p) is an antibacterial agent. Antibacterial agent 234 (6p) exhibits good activity against Klebsiella pneumoniae with a MIC value of 6.25 µg/mL.
    Antibacterial agent 234
  • HY-N14507
    Mycinamicin VII
    		Inhibitor
    Mycinamicin VII is a macrolide antibiotic. Mycinamicin VII shows activity against Gram-positive bacteria.
    Mycinamicin VII
  • HY-121104A
    Bactobolin hydrochloride
    		Inhibitor
    Bactobolin hydrochloride (Compound 1) is an antibiotic, which inhibits Escherichia coli, Salmonella, Shigella, Staphylococcus and Bacillus subtilis, with MICs of 0.3-6.25 μg/mL. Bactobolin hydrochloride exhibits antitumor efficacy against leukemia, with a LD50 value of 6.25-12.5 mg/kg.
    Bactobolin hydrochloride
  • HY-B0226A
    (E)-Nitrofurazone
    		Inhibitor 98.83%
    (E)-Nitrofurazone ((E)-Nitrofural) is a topical broad-spectrum antibacterial agent effective against both Gram-negative and Gram-positive bacteria. (E)-Nitrofurazone also possesses antiprotozoal and antiparasitic activities. (E)-Nitrofurazone is commonly used in the research of superficial wounds, burns, skin infections, pyoderma, infectious skin diseases, trypanosomiasis, and acute bacillary dysentery.
    (E)-Nitrofurazone
  • HY-B0330DR
    (R)-Ofloxacin (Standard)
    		Inhibitor
    (R)-Ofloxacin (Standard) is the analytical standard of (R)-Ofloxacin (HY-B0330D). (R)-Ofloxacin is the dextrorotatory enantiomer of Ofloxacin (HY-B0125) and is an orally effective fluoroquinolone antibiotic. (R)-Ofloxacin can inhibit the activity of bacterial DNA topoisomerase II, interfere with bacterial DNA replication and repair, and exert a bactericidal effect. (R)-Ofloxacin has a broad-spectrum antibacterial activity and has inhibitory effects on both Gram-negative and Gram-positive bacteria.
    (R)-Ofloxacin (Standard)
  • HY-119626
    Dihydrodaunomycin
    		Inhibitor
    Dihydrodaunomycin has antibacterial and antitumor activities.
    Dihydrodaunomycin
  • HY-126046
    ACP1b
    		Inhibitor
    ACP1b is an activator for ClpP protease with Kd of 3.2 μM, and exhibits antibacterial activity. ACP1b inhibits N. meningitidis and H. influenzae with MBC of 16 and 8 μg/mL.
    ACP1b
  • HY-N14955
    3-O-α-D-Forosaminyl-(+)-griseusin
    		Inhibitor
    3-O-α-D-Forosaminyl-(+)-griseusin is a memberof naphthoquinone antibiotic. 3-O-α-D-Forosaminyl-(+)-griseusin is active against Gram-positive bacteria including methicillin-resistant strain of Staphylococcus aureus (MRSA).
    3-O-α-D-Forosaminyl-(+)-griseusin
  • HY-115159
    Ro 14-9578
    		Inhibitor
    Ro 14-9578 is a tricyclic quinolone analog with antibacterial activity. Ro 14-9578 inhibits DNA biosynthesis (IC50=117 μM) and DNA supercoiling (IC50=66.8 μM) in Escherichia coli. Furthermore, Ro 14-9578 exhibits inhibitory effects against various Gram-negative bacteria and Staphylococcus aureus.
    Ro 14-9578
  • HY-N14315
    Ochracenomicin A
    		Inhibitor
    Ochracenomicin A has a strong effect against Gram-positive bacteria (including MRSA strain), and also against Gram-negative bacteria and candida albicans.
    Ochracenomicin A
  • HY-N14684
    Griseusin B
    		Inhibitor
    Griseusin B is a quinone antibiotic. Griseusin B mainly has anti-Gram-positive bacterial activity.
    Griseusin B
  • HY-W141876R
    DL-2-Aminopimelic Acid (Standard)
    		Inhibitor
    DL-2-Aminopimelic Acid is a weak agonist of glutamate receptors and also reduces the sensitivity of leech glutamate receptors to glutamate.
    DL-2-Aminopimelic Acid (Standard)
  • HY-W441968
    L-threo-β-Hydroxyaspartic acid
    		Inhibitor
    L-threo-β-Hydroxyaspartic acid is an amino acid antibiotic. L-threo-β-Hydroxyaspartic acid has the activity of inhibiting Bacillus subtilis, Xanthomonas oryzae, Mycobacterium phlei and Botrytis cinerea.
    L-threo-β-Hydroxyaspartic acid
  • HY-17516R
    Tolfenpyrad (Standard)
    		Inhibitor
    Tolfenpyrad (Standard) is the analytical standard of Tolfenpyrad (HY-17516). This product is intended for research and analytical applications. Tolfenpyrad is an orally active insecticide, acaricide and antibacterial agent. Tolfenpyrad inhibits Complex I in the mitochondrial respiratory electron transport chain, interfering with the cell respiration process. Tolfenpyrad has significant insecticidal activity against a variety of insect pests such as H. contortus, Coccinella septempunctata. Tolfenpyrad has antibacterial activity against Francisella novicida, with an IC50 of 1.2 µM or 1.5 µM.
    Tolfenpyrad (Standard)
  • HY-156456
    Elastase LasB-IN-1
    		Inhibitor
    Elastase LasB-IN-1 (Compound 4b) has antibacterial activity. Elastase LasB-IN-1 (Compound 4b) is a selective elastase LasB inhibitor with an IC50 value of 76 nM.
    Elastase LasB-IN-1
  • HY-N5167
    Argimicin A
    		Inhibitor
    Argimicin A is an antibiotic that can be isolated from Sphingomonas sp.. Argimicin A exhibits algicidal activity against toxic cyanobacteria, inhibits M. viridis and M. aeruginosa with IC50s of 12 ng/mL and 100 ng/mL.
    Argimicin A
  • HY-131102R
    Mequindox (Standard)
    		Inhibitor
    Mequindox (Standard) is the analytical standard of Mequindox. This product is intended for research and analytical applications. Mequindox is an antimicrobial agent. Mequindox acts as an inhibitor of DNA synthesis. Mequindox induces genotoxicity and carcinogenicity in mice.
    Mequindox (Standard)
  • HY-N14919
    Olivanic acid
    		Inhibitor
    Olivanic acid is a β -lactam antibiotic. Olivanic acid has the effect of anti -Gram-positive bacteria and anti-Gram-negative bacteria. Olivanic acid inhibits β-lactamase.
    Olivanic acid
  • HY-B0395S
    Sitafloxacin-d4
    		Inhibitor
    Sitafloxacin-d4 (DU6859a-d4) is deuterium labeled Sitafloxacin. Sitafloxacin (DU6859a) is a potent, orally active fluoroquinolone antibiotic. Sitafloxacin shows antichlamydial activity and antibacterial activities against a broad range of gram-positive and gram-negative bacteria, including anaerobic bacteria, as well as against atypical pathogens. Sitafloxacin can be used for the research of respiratory tract infection and urinary tract infection.
    Sitafloxacin-d<sub>4</sub>
Cat. No. Product Name / Synonyms Application Reactivity