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-167256
    Gentamicin C1
    		Inhibitor
    Gentamicin C1 is a broad-spectrum aminoglycoside antibiotic with antimicrobial activity.
    Gentamicin C1
  • HY-N13977
    Carpetimycin A
    		Inhibitor
    Carpetimycin A has very strong activity against Gram-positive and negative bacteria (including β-lactamase producing bacteria). Carpetimycin A has a strong inhibitory effect on β-lactamase.
    Carpetimycin A
  • HY-181647
    LasB-IN-3
    		Inhibitor
    LasB-IN-3 is a protease elastase (LasB) inhibitor of Pseudomonas aeruginosa with an IC50 value of 8.5 nM. LasB-IN-3 shows an IC50 of 58.9 nM for the Met128Val mutant. LasB-IN-3 binds to active sites of wild-type and Met128Val mutant LasB, coordinates zinc ions, forms hydrogen bonds and CH-π interactions, and inhibits LasB proteolytic activity. LasB-IN-3 increases survival rate in LasB-induced acute lung injury mice models. LasB-IN-3 can be used for the research of Pseudomonas aeruginosa infection.
    LasB-IN-3
  • HY-108021
    HT-61
    		Inhibitor
    HT-61 is a quinolone antibacterial agent. HT-61 exhibits bactericidal activity against gram-positive bacteria including methicillin-susceptible Staphylococcus aureus (MSSA) and methicillin-resistant Staphylococcus aureus (MRSA). HT-61 can enhance the effect of Tobramycin (HY-B0441) against Pseudomonas aeruginosa.
    HT-61
  • HY-W131122
    1,3,4-Oxadiazole
    		Inhibitor 99.79%
    1,3,4-Oxadiazoles are a class of synthetic compounds with important medicinal value, which show a variety of biological activities such as anticonvulsant, antidepressant, analgesic, anti-inflammatory, antiallergic, antipsychotic, antimicrobial, antituberculous, antitumor, and antiviral. 1,3,4-Oxadiazole derivatives need to be further developed.
    1,3,4-Oxadiazole
  • HY-W983371A
    10(S)-Hydroxystearic acid
    10(S)-Hydroxystearic acid ((S)-10-Hydroxyoctadecanoic acid; (S)-10-HSA) is a hydroxy fatty acid and a derivative of Oleic acid (HY-N1446). 10(S)-Hydroxystearic acid can be used for the research of infection.
    10(S)-Hydroxystearic acid
  • HY-W654130
    Daunorubicin-13C,d3
    		Inhibitor
    Daunorubicin-13C,d3 is 13C and deuterium labeled Daunorubicin. Daunorubicin (Daunomycin) is a topoisomerase II inhibitor with potent anti-tumor activity. Daunorubicin inhibits DNA and RNA synthesis. Daunorubicin is a cytotoxin that inhibits cancer cell viability and induces apoptosis and necrosis. Daunorubicin is also an anthracycline antibiotic. Daunorubicin can be used in the research of infection and variety of cancers, including leukemia, non-Hodgkin lymphomas, Ewing's sarcoma, Wilms' tumor.
    Daunorubicin-<sup>13</sup>C,d<sub>3</sub>
  • HY-N13969
    Arylomycin A5
    		Inhibitor
    Arylomycin A5 is a lipohexapeptide antibiotic against Gram-positive bacteria.
    Arylomycin A5
  • HY-106472
    Tioxaprofen
    		Inhibitor
    Tioxaprofen is a new anti-mycotic drug against Trichophyton mentagrophytes and T. rubrum, and is a potent uncoupling agent of mitochondrial respiration.
    Tioxaprofen
  • HY-106705
    Apalcillin sodium
    		Inhibitor
    Apalcillin (PC-904) (sodium) is an antibacterial agent. Apalcillin (sodium) is active against carbenicillin- and ampicillin-resistant strains of gram-negative bacilli.
    Apalcillin sodium
  • HY-B0395E
    (1S,2R,7S)-Sitafloxacin
    (1S,2R,7S)-Sitafloxacin (DU-6856) is an enantiomer of Sitafloxacin (HY-B0395). (1S,2R,7S)-Sitafloxacin is a topoisomerase inhibitor. (1S,2R,7S)-Sitafloxacin is an antibiotic. (1S,2R,7S)-Sitafloxacin has inhibitory activity against Escherichia coli DNA gyrase (IC50 0.18 μg/mL) and Staphylococcus aureus topoisomerase IV. (1S,2R,7S)-Sitafloxacin has antibacterial activity and can be used in the study of various bacterial infections.
    (1S,2R,7S)-Sitafloxacin
  • HY-B1802CR
    Tosufloxacin tosylate (Standard)
    		Inhibitor
    Tosufloxacin (tosylate) (Standard) is the analytical standard of Tosufloxacin (tosylate). This product is intended for research and analytical applications. Tosufloxacin (A-61827) tosylate is an orally active fluoroquinolone antibiotic. Tosufloxacin tosylate shows a broad spectrum of antibacterial activity against gram-positive and gram-negative bacteria.
    Tosufloxacin tosylate (Standard)
  • HY-D0024S1
    Sudan I-d6
    Sudan I-d6 is the deuterium labeled Sudan I (HY-D0024). Sudan I (Solvent Yellow 14) is a diazo-conjugate red dye and can be used as an additive to products such as oils, solvents or polishes. Sudan I inhibits growth of bacterial strains Clostridium perfringens and L. rhamnosus.
    Sudan I-d<sub>6</sub>
  • HY-N14806
    Napyradiomycin C1
    		Inhibitor
    Napyradiomycin C1 is an antibiotic with anti-Gram-positive bacteria and mycobacterial activity. Napyradiomycin C1 almost none to Gram-negative bacteria and fungi. IC50 (μg/mL) of leukemia L-1210 cells is 9.2.
    Napyradiomycin C1
  • HY-W014612S
    Eugenol acetate-d3
    		Inhibitor
    Eugenol acetate-d3 is the deuterated labeled Eugenol acetate (HY-W014612). Eugenol acetate (Eugenyl acetate) is an antibacterial, anticancer, anti-inflammatory and antioxidant. Eugenol acetate inhibits NF-κB and enhances the expression of p53 and p21 (WAF1). Eugenol acetate can prevent chemically induced skin cancer, inhibit cancer cell proliferation and induce apoptosis.
    Eugenol acetate-d<sub>3</sub>
  • HY-N13894
    Auramycin A
    		Inhibitor
    Auramycin A, an anthracycline antibiotic that shows marked antibacterial activity against Gram-positive bacteria. Auramycin A also exhibits antitumor activity against P388 and L1210 leukemia in mice.
    Auramycin A
  • HY-B0888
    Sulfacetamide sodium monohydrate
    		Inhibitor 99.76%
    Sulfacetamide (Sulphacetamide) sodium monohydrate is a sulfonamide antibiotic that can be used for the study of ocular infections. Sulfacetamide sodium monohydrate has antifungal and antibacterial activities.
    Sulfacetamide sodium monohydrate
  • HY-108062R
    BLI-489 (Standard)
    		Inhibitor
    BLI-489 (Standard) is the analytical standard of BLI-489 (HY-108062). This product is intended for research and analytical applications. BLI-489 is a beta-lactamase inhibitor. BLI-489 combined with Piperacillin (HY-B1923) inhibits infection caused by class A (including ultra-broad spectrum β-lactamase), Class C (AmpC) and Class D β-lactamase expressing pathogens.
    BLI-489 (Standard)
  • HY-B1606
    Chlorothymol
    		Inhibitor 99.70%
    Chlothymol is a potent positive modulator of the GABAA receptor subunit LGC-37, anticonvulsant, and antibacterial agent. Chlothymol inhibits Pentylenetetrazol-induced c-fos expression. Chlothymol inhibits the growth of Methicillin (HY-121544)-resistant Staphylococcus aureus (MRSA) strains, including LAC, with an MIC of 32 μg/mL. Chlorothymol has protective effects against epileptic seizures in various mouse models.
    Chlorothymol
  • HY-176750
    HMRZ-62
    		Inhibitor
    HMRZ-62 is an antibacterial agent. HMRZ-62 exhibits antibacterial activity against Methicillin (HY-121544)-resistant Staphylococcus aureus (MRSA) and Vancomycin (HY-B0671)-resistant Enterococcus faecalis (VRE).
    HMRZ-62
Cat. No. Product Name / Synonyms Application Reactivity