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-163967
    Clindamycin 2,4-diphosphate
    		Inhibitor
    Clindamycin 2,4-diphosphate is a related impurity of Clindamycin phosphate (HY-B1064), a prodrug of Clindamycin (HY-B1455). Clindamycin phosphate inhibits protein synthesis by targeting the bacterial ribosomal 50S subunit.
    Clindamycin 2,4-diphosphate
  • HY-125653
    Kapurimycin A2
    		Inhibitor
    Kapurimycin A2 is an antitumor antibiotic that can be found in the culture of Streptomyces sp.. Kapurimycin A2 is an active against bacteria, particularly Gram-positive organisms.
    Kapurimycin A2
  • HY-N10282
    Isodihydroauroglaucin
    		Inhibitor
    Isodihydroauroglaucin, a fungal metabolite, shows antibacterial activity.
    Isodihydroauroglaucin
  • HY-112176R
    Kanosamine hydrochloride (Standard)
    		Inhibitor
    6-Hydroxytropinone (Standard) is the analytical standard of 6-Hydroxytropinone. This product is intended for research and analytical applications. 6-Hydroxytropinone is a Alkaloids product that can be isolated from the roots of Atropa belladonna.
    Kanosamine hydrochloride (Standard)
  • HY-19050
    BRL-42715
    		Inhibitor
    BRL-42715 is a potent inhibitor of a broad range of bacterial beta-lactamases (β-lactamase) .
    BRL-42715
  • HY-N19072
    Murraya koenigii extract
    Murraya koenigii extract is derived from the leaves of the Murraya koenigii tree. Its active ingredients include alkaloids, flavonoids, terpenoids, and phenolic acids, which give it antioxidant, anti-inflammatory, and antibacterial properties.
    Murraya koenigii extract
  • HY-167906
    Lunamarine
    Lunamarine is a inhibitor of PDE5 with BBB permeability. Lunamarine can be used in the reseach of Pulmonary Arterial Hypertension (PAH) and Erectile Dysfunction (ED).
    Lunamarine
  • HY-155973
    Urease-IN-8
    		Inhibitor
    Urease-IN-8 (Compound 5e) is a competitive Urease inhibitor (IC50: 3.51 μM, Ki: 3.11 μM). Urease-IN-8 can be used for research of peptic and gastric ulcers.
    Urease-IN-8
  • HY-177773
    5-Hydroxymethyl flucloxacillin
    		Inhibitor
    5-Hydroxymethyl flucloxacillin is an active metabolite of Flucloxacillin (HY-A0246). 5-Hydroxymethyl flucloxacillin exhibits antibacterial activity.
    5-Hydroxymethyl flucloxacillin
  • HY-151599
    Pks13-TE inhibitor 3
    		Inhibitor
    Pks13-TE inhibitor 3 (compound 23) is a 13-Thioesterase (Pks13-TE) inhibitor (IC50=1.55 μM). Pks13-TE inhibitor 3 shows good anti-tuberculosis activity against both agent-sensitive and drug-resistant Mtb strains (MIC=0.0625-0.25 μg/mL). Pks13-TE inhibitor 3 can be used in studies of multidrug-resistant TB and extensively drug-resistant TB.
    Pks13-TE inhibitor 3
  • HY-128850S5
    N-Acetyl-D-mannosamine-15N
    N-Acetyl-D-mannosamine-15N is the 15N labeled N-Acetyl-D-mannosamine. N-Acetyl-D-mannosamine (ManNAc) is an essential precursor of N-acetylneuraminic acid (NeuAc), the specific monomer of bacterial capsular polysialic acid (PA)
    N-Acetyl-D-mannosamine-<sup>15</sup>N
  • HY-123024
    Cefatrizine
    		Inhibitor
    Cefatrizine (BL-S-640) is an orally active and broad-spectrum cephalosporin antibiotic. Cefatrizine is also a eEF2K inhibitor, with anti-proliferative activity in human breast cancer cells, which could induce ER stress, leading to cell death. Cefatrizine can be used in studies of cancer and bacterial infection.
    Cefatrizine
  • HY-123319A
    Antofloxacin
    		Inhibitor
    Antofloxacin is a well tolerate, orally active and broad-spectrum 8-amino-fluoroquinolone with potent antibacterial activities. Antofloxacin shows superior antibacterial activity against gyrA mutation-positive H. pylori strains, especially in Asn87- mutated strains, compared to levofloxacin. Antofloxacin is a weak, reversible inhibitor of CYP1A2 for the research of infections caused by a diverse group of bacterial species.
    Antofloxacin
  • HY-124923R
    Lupulone (Standard)
    		Inhibitor
    Lupulone (Standard) is the analytical standard of Lupulone. This product is intended for research and analytical applications. Lupulone is a beta-acid from the hop plant H. lupulus with diverse biological activities including antibacterial, antioxidant, and anticarcinogenic properties.
    Lupulone (Standard)
  • HY-N1944S
    Nerolidol-d4
    		Inhibitor
    Nerolidol-d4 is deuterated labeled Nerolidol (HY-N1944). Nerolidol has multiple natural membrane activities, possesses anti-cancer, anti-inflammatory, antibacterial and anti-insect activity. Nerolidol Suppresses parasitic activity, suppresses bloodsucking diseases, bloodworm diseases, and other diseases. Nerolidol can protect the cells from lipid and protein properties, damage to DNA, and protect the cells from damage.
    Nerolidol-d<sub>4</sub>
  • HY-120315
    Nyssoside
    		Inhibitor
    Nyssoside, a ellagic acid derivative, has significant antioxidant activity and shows antibacterial activity against different pathogenic bacteria.
    Nyssoside
  • HY-W714047
    Valerianol
    		Inhibitor
    Valerianol is a sesquiterpene alcohol with anticancer, antibacterial, and antiviral activities. Valerianol selectively inhibits TPA (HY-18739)-induced Epstein-Barr virus early antigen (EBV-EA) activation (IC50=300 μM). Valerianol inhibits tumor promoter-mediated EBV-EA activation and also inhibits pathogenic bacteria such as Staphylococcus aureus.
    Valerianol
  • HY-A0166AR
    Cilastatin sodium (Standard)
    		Inhibitor
    Cilastatin (sodium) (Standard) is the analytical standard of Cilastatin (sodium). This product is intended for research and analytical applications. Cilastatin sodium (MK0791 sodium) is a reversible, competitive renal dehydropeptidase I inhibitor with an IC50 of 0.1 μM. Cilastatin sodium inhibits the bacterial metallob-lactamase enzyme CphA with an IC50 of 178 μM. Cilastatin sodium is an antibacterial adjunct[1][2][3].
    Cilastatin sodium (Standard)
  • HY-N14257
    Andrimid
    		Inhibitor
    Andrimid is a peptide Antibiotic and acetyl-CoA carboxylase inhibitor. Andrimid is produced by symbiotic bacteria of the genus *Enterobacter* residing in the brown planthopper Nilaparvata lugens. Andrimid exhibits strong specific activity against Xanthomonas campestris pv. oryzae. Andrimid shows no or only weak activity against Gram-positive and Gram-negative bacteria, including most plant pathogenic bacteria. Andrimid can be used in studies related to bacterial infections and rice bacterial blight.
    Andrimid
  • HY-N0465S
    Olaquindox-d4
    		Inhibitor
    Olaquindox-d4 is the deuterium labeled Olaquindox (HY-N0465). Olaquindox, a quinoxalin derivative, is an orally active antibiotic. Olaquindox stimulates growth and decreases intestinal mucosal immunity of piglets.
    Olaquindox-d<sub>4</sub>
Cat. No. Product Name / Synonyms Application Reactivity