Oxolinic acidOxolinic acid - High-quality laboratory reagent available from Gentaur. Catalog: 804-HY-B1002-01.804-HY-B1002-01804-HY-B1002-01Business & Industrial > Science & LaboratoryOxolinic acid
Gentaur
EUR12027-02-24

Oxolinic acid

CAT:
804-HY-B1002-01
Size:
500 mg
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
Oxolinic acid - image 1

Oxolinic acid

  • Description:

    Oxolinic acid is an antibiotic against both Gram-negative and Gram-positive bacteria. Oxolinic acid can be used for the research of acute and chronic urinary tract infections. Oxolinic acid is a DNA/RNA synthesis inhibitor. Oxolinic acid acts a dopamine uptake inhibitor and stimulants locomotor effect in mice[1][2][3].
  • UNSPSC:

    12352005
  • Hazard Statement:

    H302
  • Target:

    Antibiotic; Bacterial; DNA/RNA Synthesis
  • Type:

    Reference compound
  • Related Pathways:

    Anti-infection; Cell Cycle/DNA Damage
  • Applications:

    COVID-19-anti-virus
  • Field of Research:

    Infection
  • Assay Protocol:

    https://www.medchemexpress.com/Oxolinic-acid.html
  • Purity:

    99.10
  • Solubility:

    0.5 M NaOH : ≥ 50 mg/mL|DMSO : 1 mg/mL (ultrasonic) |H2O : < 0.1 mg/mL
  • Smiles:

    O=C(C1=CN(CC)C2=C(C=C3C(OCO3)=C2)C1=O)O
  • Molecular Formula:

    C13H11NO5
  • Molecular Weight:

    261.23
  • Precautions:

    H302
  • References & Citations:

    [1]M J Kershaw, et al. The antibacterial and pharmacological activity of oxolinic acid (Prodoxol) . J Antimicrob Chemother. 1975 Sep;1 (3) :311-5.|[2]S H Manes, et al. Inhibition of RNA synthesis by oxolinic acid is unrelated to average DNA supercoiling. J Bacteriol. 1983 Jul; 155 (1) : 420-423.|[3]J Garcia de Mateos-Verchere, et al. Behavioural and neurochemical evidence that the antimicrobial agent oxolinic acid is a dopamine uptake inhibitor. Eur Neuropsychopharmacol. 1998 Dec;8 (4) :255-9.
  • Shipping Conditions:

    Room Temperature
  • Storage Conditions:

    -20°C, 3 years; 4°C, 2 years (Powder)
  • Scientific Category:

    Reference compound1
  • Clinical Information:

    No Development Reported
  • CAS Number:

    [14698-29-4]