Chlorzoxazone

CAS No. 95-25-0

Chlorzoxazone ( NSC 26189 )

Catalog No. M16810 CAS No. 95-25-0

Chlorzoxazone is a centrally acting muscle relaxant used to treat muscle spasm and the resulting pain or discomfort.

Purity : >98%(HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
500MG 38 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Chlorzoxazone
  • Note
    Research use only, not for human use.
  • Brief Description
    Chlorzoxazone is a centrally acting muscle relaxant used to treat muscle spasm and the resulting pain or discomfort.
  • Description
    Chlorzoxazone is a centrally acting muscle relaxant used to treat muscle spasm and the resulting pain or discomfort. It acts on the spinal cord by depressing reflexes.Chlorzoxazone is currently being used as a marker substrate in vitro/vivo studies to quantify cytochrome P450 2E1 (CYP2E1) activity in humans.
  • Synonyms
    NSC 26189
  • Pathway
    Cell Cycle/DNA Damage
  • Target
    Potassium Channel
  • Recptor
    Potassium Channel
  • Research Area
    Inflammation/Immunology
  • Indication
    ——

Chemical Information

  • CAS Number
    95-25-0
  • Formula Weight
    169.57
  • Molecular Formula
    C7H4ClNO2
  • Purity
    >98%(HPLC)
  • Solubility
    Ethanol: 34 mg/mL (200.5 mM); DMSO: 34 mg/mL (200.5 mM)
  • SMILES
    C1=CC2=C(C=C1Cl)NC(=O)O2
  • Chemical Name
    5-chloro-3H-1,3-benzoxazol-2-one

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1.Dong DL, et al. Eur J Pharmacol. 2006 Sep 18;545(2-3):161-6.
molnova catalog
related products
  • Nicorandil

    Nicorandil(Ikorel)is potassium channel activator. It acts by relaxing the smooth muscle of the blood vessels, especially those of the venous system.

  • MonoMethyl auristati...

    Monomethyl auristatin F, an antimitotic agent, inhibits cell division by blocking the polymerization of tubulin.

  • Gut restricted-7

    Gut restricted-7 (GR-7) is a covalent and orally active pan-bile salt hydrolase (BSH) inhibitor. It decreases gut bacterial BSHs and decreases deconjugated bile acid levels in the feces of mice.