2. Signaling Pathways
  3. Anti-infection
  4. Antibiotic
  5. Antibiotic Inhibitor

Antibiotic Inhibitor

Antibiotic Isoform Comparison

Antibiotic Inhibitors (33):

Cat. No. Product Name Effect Purity
  • HY-N0113B
    Hordenine hydrochloride
    		Inhibitor 99.82%
    Hordenine (hydrochloride), an alkaloid found in?plants, inhibits melanogenesis by suppression of cyclic adenosine monophosphate (cAMP) production.
  • HY-B1924
    Norvancomycin hydrochloride
    		Inhibitor
    Norvancomycin hydrochloride is suitable for endocarditis, osteomyelitis, pneumonia, sepsis or soft tissue infections caused by Staphylococcus aureus (including methicillin-resistant strains and multi-drug-resistant strains).
  • HY-105048
    Omiganan
    		Inhibitor 99.15%
    Omiganan is a cationic antimicrobial peptide. Omiganan as an analogue of indolicidin shows activity against gram-positive and gram-negative bacteria but also Candida spp. isolates. Omiganan can be used for the research of alcohol nose and acne.
  • HY-B1118
    Secnidazole
    		Inhibitor 99.87%
    Secnidazole (RP-14539) is an orally active azole antibiotic and a imidazole mitigator of Serratia marcescens virulence. Secnidazole, as an analog of acylhomoserine lactones, effectively inhibits QS resulting in the attenuation of Pseudomonas aeruginosa pathogenesis. Secnidazole has antimicrobial activity against many anaerobic Gram-negative and Gram-positive bacterial species in vitro. Secnidazole can be used for the research of various diseases, such as amoebiasis and giardiasis, and bacterial vaginitis.
  • HY-131150
    Ristomycin sulfate
    		Inhibitor 98.08%
    Ristomycin sulfate is a glycopeptide antibiotic isolated from Nocardia lurida.
  • HY-146331
    PC190723
    		Inhibitor 98.34%
    PC190723 (Compound 2) is an inhibitor of the bacterial cell division protein FtsZ with an IC50 of 55 ng/ml. FtsZ-IN-3 exhibits anti-staphylococcal activity with MIC values of 1 µg/ml for MSSA and MRSA.
  • HY-131146
    AMOZ
    		Inhibitor
    AMOZ, a tissue bound metabolite of Furaltadone, Furaltadone is a synthetic nitrofuran antibiotic widely used
  • HY-N10229
    Harzianum A
    		Inhibitor
    Harzianum A is a trichothecene that isolated from the soil-borne fungus Trichoderma harzianum. Harzianum A shows no cytotoxicity against baby hamster kidney cells, no activity against Gram-negative and Gram-positive bacteria, but modest antifungal activity at 100 μg/mL.
  • HY-B1118A
    Secnidazole hemihydrate
    		Inhibitor
    Secnidazole (RP-14539) hemihydrate is an orally active azole antibiotic and a imidazole mitigator of Serratia marcescens virulence. Secnidazole hemihydrate, as an analog of acylhomoserine lactones, effectively inhibits QS resulting in the attenuation of Pseudomonas aeruginosa pathogenesis. Secnidazole hemihydrate has antimicrobial activity against many anaerobic Gram-negative and Gram-positive bacterial species in vitro. Secnidazole hemihydrate can be used for the research of various diseases, such as amoebiasis and giardiasis, and bacterial vaginitis.
  • HY-W154333
    H-Arg-OtBu dihydrochloride
    		Inhibitor
    H-Arg-OtBu (dihydrochloride) is a membrane-targeting antimicrobial. H-Arg-OtBu (dihydrochloride) targets the negatively charged bacterial membrane via a combination of electrostatic and hydrophobic interactions. H-Arg-OtBu (dihydrochloride) can be used for bacterial infections diseases research.
  • HY-124551
    Viridiol
    		Inhibitor
    Viridiol, a fungal metabolite from Trichodernza viride, shows antifungal activity.
  • HY-P3384
    Pezadeftide
    		Inhibitor
    Pezadeftide is a potent antifungal peptide. Pezadeftide can enter fungal cells and cause a rapid mitochondrial response that results in hyperpolarization of the mitochondrial membrane.
  • HY-150583
    Chitin synthase inhibitor 2
    		Inhibitor
    Chitin synthase inhibitor 2 (compound 2b) is a potent inhibitor of chitin synthase with the IC50 value of 0.09 mM and the Ki value of 0.12 mM. Chitin synthase inhibitor 2 has antimicrobial activities in vitro and shows synergistic or additive effects with fluconazole or polyoxin B.
  • HY-118512
    Platencin
    		Inhibitor
    Platencin is a natural, broad spectrum Gram-positive antibiotic isolated from S. platensis. Platencin inhibits β-ketoacyl-ACP synthases II and III (FabF and FabH, respectively) with IC50s of 1.95 and 3.91 μg/ml, respectively.
  • HY-E70140
    α-1,4-N-Acetylglucosaminyltransferase 4
    		Inhibitor
    α-1,4-N-Acetylglucosaminyltransferase 4 (EC 2.4.1, A4GNT) catalyzes the transfer of N-acetylglucosamine (GlcNAc) to core 2 branched O-glycans and suppresses H. pylori growth.
  • HY-P2323
    Lactoferricin B (4-14), bovine TFA
    		Inhibitor
    Lactoferricin B (4-14), bovine (TFA), a peptide corresponding to residues 4-14 of bovine lactoferrin, has antimicrobial activity against a wide range of microorganisms.
  • HY-N10223
    Phostriecin
    		Inhibitor
    Phostriecin is an antitumor antibiotic produced by Streptomyces pulveraceus. Phostriecin is a strong inhibitor of type 2A (PP2A) and a weak inhibitor of type 1 (PP1) serine/threonine protein phosphatases with IC50s of 3.2 nM and 131 μM, respectively. Phostriecin has the potential for the research of cancer.
  • HY-131144S
    AMOZ-d5
    		Inhibitor 99.0%
    AMOZ-d5 is a deuterium labeled AMOZ. AMOZ, a tissue bound metabolite of Furaltadone, Furaltadone is a synthetic nitrofuran antibiotic widely used[1].
  • HY-B1252
    Cefalonium
    		Inhibitor
    Cefalonium is the first-generation β-lactam cephalosporin antibiotic that is widely used to research bovine mastitis caused by Gram-positive bacteria including staphylococci.
  • HY-135181
    Daunosamnyl-daunorubicin
    		Inhibitor
    Daunosamnyl-daunorubic, an antibiotic, can bind calf thymus DNA.