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-N13890
    Arginomycin
    		Inhibitor
    Arginomycin is a nucleoside antibiotic that inhibits the growth of Gram-positive bacteria and fungi in vitro.
    Arginomycin
  • HY-N0913AR
    Isomaltotriose (Standard)
    Isomaltotriose (Standard) is the analytical standard of Isomaltotriose. This product is intended for research and analytical applications. Isomaltotriose is a type of isomaltooligosaccharide belonging to the α-glucan family. Isomaltotriose acts not only as an important prebiotic component that can be differentially metabolized by beneficial intestinal bacteria to regulate the intestinal flora, but also as a valuable chemical synthesis precursor that can be modified enzymatically to introduce hydrophobic groups and converted into high-value functional molecules.
    Isomaltotriose (Standard)
  • HY-N14467
    Pneumocandin A4
    		Inhibitor
    Pneumocandin A4 is a lipopeptide antibiotic. Pneumocandin A4 has a strong anti-Candida effect. Pneumocandin A4 has the effect of inhibiting the synthesis of 1,3 early-glucan in vitro, with an IC50 of 0.07-0.5 μg/mL.
    Pneumocandin A4
  • HY-N13900
    Arisostatin B
    		Inhibitor
    Arisostatin B is a Tetrocarcin class of antibiotic against Gram-positive bacteria and antitumor activity.
    Arisostatin B
  • HY-N15140
    α-Thujaplicin
    		Inhibitor
    α-Thujaplicin, the isomer of Hinokitiol (HY-B2230), is an antimicrobial agent. α-Thujaplicin can be isolated from Aomori Hiba (Thujopsis dolabrata SIEB. et ZUCC. var. hondai MAKINO). α-Thujaplicin shows inhibition of Carboxypeptidase A (IC50: 32.4 μM). α-Thujaplicin shows rather strong antifungal activity against seven kinds of plant-pathogenic fungi, their MICs being in the range of 12.0-50.0 μg/mL. α-Thujaplicin shows clear antibacterial activity against Legionella pneumophila SG 1 and L. pneumophila SG 3, and their MICs are in the range of 12.5-50 μg/mL. α-Thujaplicin shows antibacterial activity against Enterococcus faecalis IFO-12965 with a MIC of 1.56 μg/mL. α-Thujaplicin shows germination inhibition toward the seed of Echinochloa utilis Ohwi et Yabuno. α-thujaplicin inhibits lymphocytic leukemia, stomach cancer, Ehrlich’s ascites carcinoma.
    α-Thujaplicin
  • HY-N0078R
    Ginkgolic Acid (C13:0) (Standard)
    		Inhibitor
    Ginkgolic Acid (C13:0) (Standard) is the analytical standard of Ginkgolic Acid (C13:0) (HY-N0078). This product is intended for research and analytical applications. Ginkgolic Acid (C13:0) (Ginkgoneolic Acid) is an anti-cariogenic agent and a PI3Kδ inhibitor (IC50: 2.49 μM). Ginkgolic Acid (C13:0) exhibits antibacterial and anti-parasitic activities. Ginkgolic Acid (C13:0) can also inhibit mast cell degranulation (IC50: 2.40 μM).
    Ginkgolic Acid (C13:0) (Standard)
  • HY-N14610
    Grahamimycin B
    		Inhibitor
    Grahamimycin B has weak activity against Gram-positive bacteria, negative bacteria, cyanobacteria and green algae.
    Grahamimycin B
  • HY-N14575
    Pyrrolomycin B
    		Inhibitor
    Pyrrolomycin B is a pyrrole antibiotic. Pyrrolomycin B has anti-Gram-positive bacteria, anti-Gram-negative bacteria and anti-individual fungi activity.
    Pyrrolomycin B
  • HY-N14025
    Chicamycin B
    		Inhibitor
    Chicamycin B has anti-tumor activity and weak anti-Gram-positive bacteria activity.
    Chicamycin B
  • HY-161803
    Anti-MRSA agent 12
    		Inhibitor
    Anti-MRSA agent 12 (Compound SM-5) is an antibiotic, which exhibits antibacterial activity against Staphylococcus aureus, S. epidermidis and Escherichia coli with MIC of 7.81, 7.81 and 62.5 μM. Anti-MRSA agent 12 inhibits the methicillin-resistant S. aureus (MRSA) through inhibition of biofilm formation.
    Anti-MRSA agent 12
  • HY-N14861
    Neoviridogrisein Ⅱ
    		Inhibitor
    Neoviridogrisein II has been used to resist Gram-positive bacteria and mycoplasma.
    Neoviridogrisein Ⅱ
  • HY-181799
    EG35
    EG35 is a nucleotide-binding domain-targeted DnaK inhibitor. EG35 binds to Escherichia coli DnaK and inhibits the ATPase activity stimulated by DnaJ and GrpE.
    EG35
  • HY-162094
    CMX410
    		Inhibitor
    CMX410 is an orally active and selective Mycobacterium tuberculosis Pks13 acyltransferase domain inhibitor and anti-bacterial agent. CMX410 reacts with the catalytic serine of the Pks13-AT domain to form a stable β-lactam ring, disables the enzyme’s active site, reduces trehalose monomycolate and trehalose dimycolate levels, triggers cell lysis, and reduces intracellular bacterial burden. CMX410 can be used for the research of tuberculosis.
    CMX410
  • HY-D2430
    Chitosan-PEG-Cy3
    		Inhibitor
    Chitosan-PEG-Cy3 is a fluorescent labeling reagent that combines Cy3 (HY-D0822) fluorescent dye, Chitosan and polyethylene glycol (PEG). The Cy3 fluorophore is commonly used in applications such as immunolabeling, nucleic acid labeling, fluorescence microscopy, and flow cytometry. Cy3 has an emission maximum around 562-570 nm. Chitosan exhibits antimicrobial activity against various bacteria and fungi.
    Chitosan-PEG-Cy3
  • HY-175228
    RNA MTase-IN-1
    		Inhibitor
    RNA MTase-IN-1 (Compound 47) is a RNA methyltransferase (RNA MTase) inhibitor with an IC50 of 68  μM for 16S rRNA (m1A1408) methyltransferase (NpmA). RNA MTase-IN-1 has a significant inhibitory activity against pathogen-associated aminoglycoside-resistance. RNA MTase-IN-1 can be used for resistant bacterial infections research.
    RNA MTase-IN-1
  • HY-14397S2
    Indometacin-d7
    Indometacin-d7 is deuterated labeled Indomethacin (HY-14397). Indomethacin (Indometacin) is a potent, orally active COX1/2 inhibitor with IC50 values of 18 nM and 26 nM for COX-1 and COX-2, respectively. Indomethacin has anticancer activity and anti-infective activity. Indomethacin can be used for cancer, inflammation and viral infection research.
    Indometacin-d<sub>7</sub>
  • HY-109796
    NIK250
    		Inhibitor
    NIK250 is a potent multiple drug resistance (MDR) reversal agent that inhibits P-glycoprotein.
    NIK250
  • HY-B2091A
    Azidocillin sodium
    		Inhibitor
    Azidocillin sodium, a semi-synthetic Penicillin, is an orally active β-lactam antibiotic. Azidocillin sodium bears an azide functionality and retains on-target activity within bacteria. Azidocillin sodium can be used to research osteitis caused by dental surgery, otitis media, enterococcal septicemia and other bacterial infectious diseases. Azidocillin sodium is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.
    Azidocillin sodium
  • HY-N14128
    Cirramycin B1
    		Inhibitor
    Cirramycin B1 has the activity against Gram-positive bacteria, Gram-negative bacteria and mycoplasmas.
    Cirramycin B1
  • HY-W755036
    Oxytetracycline-13C,d3 hydrochloride
    		Inhibitor
    Oxytetracycline-13C,d3 hydrochloride is the 13C- and deuterium labeled Oxytetracycline hydrochloride (HY-B0275A). Oxytetracycline hydrochloride is an antibiotic that exhibits board-spectrum antibacterial activity. Oxytetracycline hydrochloride is a protein synthesis inhibitor and prevents the binding from aminoacil-tRNA to the complex m-ribosomal RNA. Oxytetracycline hydrochloride also possesses anti-HSV-1 activity.
    Oxytetracycline-<sup>13</sup>C,d<sub>3</sub> hydrochloride
Cat. No. Product Name / Synonyms Application Reactivity