Zonisamide sodium salt
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
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
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. |
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