Basic information Safety Supplier Related

Zonisamide sodium salt

Basic information Safety Supplier Related

Zonisamide sodium salt Basic information

Product Name:
Zonisamide sodium salt
Synonyms:
  • ZON
  • 1,2-BENZISOXAZOLE-3-METHANESULFONAMIDE
  • BENZO[D]ISOXAZOL-3-YL-METHANESULFONAMIDE
  • 1,2-benzisoxazole-3-methanesulfonamide sodium-potassium salt
  • 1,2-Benzisoxazole-3-methanesulfonamide sodium-potassium salt, Aleviatin sodium-potassium salt, Exceglan sodium-potassium salt, Excegram sodium-potassium salt
  • 1,2-Benzisoxazole-3-methanesulfonamide sodium salt
  • Zonisamide sodium salt
  • ZonisaMide (sodiuM)
CAS:
68291-98-5
MF:
C8H7N2NaO3S
MW:
234.21
Mol File:
68291-98-5.mol
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Zonisamide sodium salt Chemical Properties

storage temp. 
Store at -20°C
solubility 
H2O: >5mg/mL
form 
powder
color 
white to beige
Water Solubility 
H2O: >5mg/mL
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22
WGK Germany 
3
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Zonisamide sodium salt Usage And Synthesis

Uses

Zonisamide Sodium Salt can be used in biological study of neuroprotective effects of zonisamide target astrocyte. It shows neuroprotection by increasing glutathione, cystine/glutamate exchange transporter expression in mouse CNS catecholaminergic, astrocyte and rat glioma cell and mouse model of 6-OHDA induced hemi-Parkinson''s disease

Biochem/physiol Actions

Zonisamide sodium salt is an anti-epileptic. It is effective in various animal epilepsy models and humans with both partial and generalized epileptic seizures. Zonisamide sodium salt also scavenges nitric oxide (NO).

in vivo

Zonisamide sodium (40 mg/kg; i.p.; single daily for 14 days) prevents seizures in FeCl3-induced chronic amygdalar seizures model[2].
Zonisamide sodium (14, 28, 56 mg/kg; i.p.; single daily for 6 weeks) alleviates cardiac hypertrophy and improved cardiac function in rats subjected to AAC (abdominal aortic constriction)[3].
Zonisamide sodium (14, 28, 56 mg/kg; i.p.; single daily for 6 weeks) upregulates Hrd1 expression and accelerates ERAD in the hearts of AAC rats[3].

Animal Model:Male Wistar rats (200-250 g; FeCl3-induced chronic amygdalar seizures)[2].
Dosage:40 mg/kg
Administration:Intraperitoneal injection; single daily for 14 days.
Result:Showed activity of anti-seizures.
Significantly down-regulated GABA transporters GAT-1 in the hippocampus.
Animal Model:Adult male Sprague-Dawley rats (100-120 g; cardiac hypertrophy model)[3].
Dosage:14, 28, 56 mg/kg (dissolved in 1% DMSO)
Administration:Intraperitoneal injection; single daily for 6 weeks.
Result:Significantly attenuated cardiac hypertrophy and fibrosis.
Increased LV ejection fraction (EF), fractional shortening (FS) and E/A ratio.
Markedly increased the expression of Hrd1 in the hearts of AAC rats.

Zonisamide sodium saltSupplier

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