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

Bacterial

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-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-N14678
    Piloquinone
    Piloquinone is a phenanthrene compound. Piloquinone has inhibitory effect on mycobacterium and protozoa, but the effect is not strong.
    Piloquinone
  • 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-125419
    Amythiamicin B
    Amythiamicin B is a trisubstituted pyridine thiopeptide with antibiotic properties against Gram-positive bacteria and activity against Plasmodium falciparum.
    Amythiamicin B
  • 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-14768S
    Favipiravir-13C15N
    Favipiravir-13C15N (T-705-13C15N) is 13C and 15N labeled Favipiravir. Favipiravir (T-705) is a potent viral RNA polymerase inhibitor, it is phosphoribosylated by cellular enzymes to its active form, Favipiravir-ribofuranosyl-5′-triphosphate (RTP). Favipiravir-RTP inhibits the influenza viral RNA-dependent RNA polymerase (RdRP) activity with an IC50 of 341 nM.
    Favipiravir-<sup>13</sup>C<sup>15</sup>N
  • 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>
  • HY-N6779R
    Patulin (Standard)
    Inhibitor
    Patulin (Standard) is the analytical standard of Patulin. This product is intended for research and analytical applications. Patulin (Terinin) is a mycotoxin produced by fungi including the Aspergillus, Penicillium, and Byssochlamys species, causes chromosome breakage, mutation, teratogenic and cytotoxic. Patulin induces autophagy-dependent apoptosis through lysosomal-mitochondrial axis, and causes DNA damage.
    Patulin (Standard)
  • HY-N14769
    2-Hydroxyaclacinomycin B
    Inhibitor
    2-Hydroxyaclacinomycin B is an anthracycline antibiotic. 2-Hydroxyaclacinomycin B can be found in Strptomyces galilaeus A-862 (FERM BP-45). 2-Hydroxyaclacinomycin B inhibits RNA synthesis and has anti-tumor activity.
    2-Hydroxyaclacinomycin B
  • HY-155096
    Antibacterial agent 149
    Inhibitor
    Antibacterial agent 149 (Compd 3j) is a laccase inhibitor with high fungicidal activity and can be used in the study of rice sheath blight.
    Antibacterial agent 149
  • HY-24547
    HpFabZ-IN-1
    Inhibitor
    HpFabZ-IN-1 is an inhibitor of β-hydroxyacyl acyl carrier protein dehydratase (FabZ). HpFabZ-IN-1 has certain antibacterial activity. HpFabZ-IN-1 can be used for research on inflammatory diseases such as gastritis.
    HpFabZ-IN-1
  • HY-N13971
    Bamicetin
    Inhibitor
    Bamicetin is mainly resistant to Gram-positive bacteria and Mycobacteria.
    Bamicetin
  • HY-175858
    Mtb-IN-13
    Inhibitor
    Mtb-IN-13 (Compound 5f) is an inhibitor of Mycobacterium tuberculosis (Mtb), with a MIC of 0.25 μg/mL. The Ki values of MTTB-in-13 for MtCA1, MtCA2, MtC, and 3 are 0.6023, 0.0780, and 0.1994 μM, respectively. Mtb-IN-13 can be used in the research of tuberculosis.
    Mtb-IN-13
  • HY-N14836
    Macquarimicin C
    Inhibitor
    Macquarimicin C is an antibiotic.
    Macquarimicin C
  • HY-114913
    Fenarimol
    Inhibitor
    Fenarimol (EL 222) is a potent and orally active fungicide. Fenarimol also is a androgen receptor inhibitor with an IC50 value of 19 µM. Fenarimol decreases the mRNA expression of PBP C3, ODC, IGF-1.
    Fenarimol
  • HY-137323
    Leucinostatin H
    Inhibitor
    Leucinostatin H is a polypeptide antibiotic discovered in Paecilomyces marquandii, characterized by a tertiary amine-oxide terminal group. Leucinostatin H exhibits inhibitory activity against Gram-positive bacteria, such as Bacillus subtilis, B. cereus, and Staphylococcus aureus (MIC 10-100 μg/mL). Leucinostatin H holds potential for research in anti-infective and plant disease control applications.
    Leucinostatin H
  • HY-N3623
    Corianin
    Inhibitor
    Corianin is a sesquiterpene lactone that can be isolated from the fruits of Coriaria ruscifolia. Corianin shows antibacterial activity against S. aureus and S. epidermis.
    Corianin
Cat. No. Product Name / Synonyms Application Reactivity