Zonisamide NEW
| Price | $40 | $59 | $79 |
| Package | 50mg | 100mg | 200mg |
| Supply Ability: | 10g |
| Update Time: | 2026-06-02 |
Product Details
| Product Name: Zonisamide | CAS No.: 68291-97-4 |
| Purity: 99.94% | Supply Ability: 10g |
| Release date: 2026/06/02 |
Product Introduction
Bioactivity
| Name | Zonisamide |
| Description | Zonisamide (AD 810), a sulfonamide anticonvulsant, is approved for use as an adjunctive treatment in adults with partial-onset seizures. It may inhibit a carbonic anhydrase although this is not one of the main mechanisms of action. Zonisamide may act by blocking repetitive firing of voltage-gated sodium channels results in a reduction of T-type calcium channel currents, or by binding allosterically to GABA receptors. This latter action may lower the uptake of the inhibitory neurotransmitter GABA while increasing the uptake of the excitatory neurotransmitter glutamate. |
| In vitro | Zonisamide inhibits monoamine oxidase B activity in vitro with an IC50 of 25 μM. |
| In vivo | Zonisamide inhibits monoamine oxidase B activity in vitro with an IC50 of 25 μM. |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature. |
| Solubility Information | DMSO : 250 mg/mL (1177.97 mM), Sonication is recommended. 10% DMSO+90% Saline : 10 mg/mL (47.12 mM), Solution. 10% DMSO+40% PEG300+5% Tween 80+45% Saline : 2 mg/mL (9.42 mM), Sonication is recommended. |
| Keywords | Zonisamide | SodiumChannel | Sodium Channel | SH-SY5Y | seizure | parkinson's disease | NRCMs | Inhibitor | inhibit | epilepsy | CI-912 | CI912 | cardiac hypertrophy | cardiac fibroblasts | CarbonicAnhydrase | Carbonic Anhydrase | Carbonate dehydratase | CalciumChannel | Calcium Channel | Apoptosis | AD-810 | AD810 |
| Inhibitors Related | Stavudine | Aceglutamide | 2,4,6-Tri-tert-butylphenol | Urea | Tamoxifen | Cysteamine hydrochloride | Sodium Dihydrogen Phosphate | Metronidazole | Formamide | Dimethyl phthalate | Alginic acid | Sildenafil citrate |
| Related Compound Libraries | Failed Clinical Trials Compound Library | Bioactive Compound Library | Anti-Neurodegenerative Disease Compound Library | Pain-Related Compound Library | Membrane Protein-targeted Compound Library | Drug Repurposing Compound Library | Inhibitor Library | FDA-Approved Drug Library | Anti-Cancer Approved Drug Library | Bioactive Compounds Library Max | Ion Channel Targeted Library | Anti-Cancer Drug Library |
Company Profile Introduction
TargetMol Chemicals Inc. is headquartered in Boston, MA, and specializes in products and services that serve the research needs of chemical and biological scientists worldwide. With a client base in 40+ countries, TargetMol has evolved into one of the biggest global research suppliers for compound libraries and small molecule compounds.
170+ Compound Libraries， 10000+ Noval Small Molecucles，16000+ Nature Compounds
TargetMol diligently updates and offers over 170 types of compound libraries and a wide range of high-quality research chemicals, including inhibitors, activators, natural products, peptides, antibodies , and novel life-science kits for laboratory and scientific use. In addition, our lab allows us to conduct CADD (computer-aided drug design) and chemical synthesis to meet the customization needs of our clients.
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