ChemSpider 2D Image | Dantrolene Sodium | C14H9N4NaO5

Dantrolene Sodium

  • Molecular FormulaC14H9N4NaO5
  • Average mass336.235 Da
  • Monoisotopic mass336.047058 Da
  • ChemSpider ID5036403
  • Charge - Charge

    Double-bond stereo - Double-bond stereo


More details:






Validated by Experts, Validated by Users, Non-Validated, Removed by Users

1-[(5-??(p-Nitro??phenyl)??fur??furyl??idene)??amino]??hydan??toin sodium salt
2,4-Imidazolidinedione, 1-[[(1E)-[5-(4-nitrophenyl)-2-furanyl]methylene]amino]-, sodium salt (1:1) [ACD/Index Name]
28F0G1E0VF
3-[(E)-{[5-(4-Nitrophényl)-2-furyl]méthylène}amino]-2,5-dioxoimidazolidin-1-ide de sodium [French] [ACD/IUPAC Name]
Dantrix [Trade name]
Dantrolene (sodium salt)
Dantrolene Sodium [BAN] [INN] [USAN]
Dantrolene Sodium (anhydrous)
Dantrolene sodium anhydrous
Dantrolene sodium salt
More...

Validated by Experts, Validated by Users, Non-Validated, Removed by Users

C07933 [DBID]
D9175_SIGMA [DBID]
EU-0100424 [DBID]
F 440 [DBID]
  • Experimental Physico-chemical Properties
    • Experimental Melting Point:

      279 °C LKT Labs [D0255]
    • Experimental Solubility:

      Slightly soluble in water; more soluble in alkaline soln. LKT Labs [D0255]
      Soluble to 10 mM in DMSO Tocris Bioscience 0507, 507
      Soluble to 5 mM in water and to 10 mM in DMSO Tocris Bioscience 0507
      Soluble to 5 mM in water with gentle warming and to 10 mM in DMSO Tocris Bioscience 0507
  • Miscellaneous
    • Target Organs:

      Calcium Channel; Ryanodine receptor antagonist TargetMol T0077
    • Therapeutical Effect:

      muscle relaxant (skeletal) Microsource [01503209]
    • Drug Status:

      USAN, INN, BAN, JAN Microsource [01503209]
    • Compound Source:

      synthetic Microsource [01503209]
    • Bio Activity:

      Ca2+ release inhibitor Tocris Bioscience 0507, 507
      Calcium Channel ; Ryanodine receptor 1 TargetMol T0077
      Calcium Channels Tocris Bioscience 507
      Inhibits release of Ca2+ from sarcoplasmic reticulum via inhibition of ryanodine receptor (RYR) channels. Displays selectivity for RYR1 and RYR3 over RYR2. Protective against the effects of a variety of conditions and agents, including excitatory amino acids. Skeletal muscle relaxant and neuroprotectant. Tocris Bioscience 0507
      Inhibits release of Ca2+ from sarcoplasmic reticulum via inhibition of ryanodine receptor (RYR) channels. Displays selectivity for RYR1 and RYR3 over RYR2. Protective against the effects of a variety of conditions and agents, including excitatory amino acids. Skeletal muscle relaxant and neuroprotectant. Tocris Bioscience 507
      Ion Channels Tocris Bioscience 507
      Membrane Transporter/Ion Channel TargetMol T0077
      Ryanodine Receptors Tocris Bioscience 507

Predicted data is generated using the ACD/Labs Percepta Platform - PhysChem Module

No predicted properties have been calculated for this compound.

Click to predict properties on the Chemicalize site






Advertisement