1188265-58-8
1188265-58-8
Chemical Structure
Zonisamide-13C2,15N
- CAS No.: 1188265-58-8
- Formula:C613C2H8N15NO3S
- Molecular Weight:215.20
IUPAC Name: (benzo[d]isoxazol-3-yl-3-13C)methanesulfonamide-13C-15N
InChIKey: UBQNRHZMVUUOMG-VDWPWFDKSA-N
SMILES: [15NH2]S([13CH2][13C]1=NOC2=CC=CC=C12)(=O)=O
Biological Activity: Zonisamide-13C2,15N is deuterated labeled Zonisamide.
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Zonisamide-13C2,15N | Zonisamide-13C2,15N is deuterated labeled Zonisamide. | |||||||||||||||||||||
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Zonisamide (Standard) | ≥98% | Zonisamide (Standard) is the analytical standard of Zonisamide. This product is intended for research and analytical applications. Zonisamide (AD 810) is an orally active carbonic anhydrase inhibitor, with Kis of 35.2 and 20.6 nM for hCA II and hCA V, respectively. Zonisamide exerts neuroprotective effects through anti-apoptosis and upregulating MnSOD levels. Zonisamide also increases the expression of Hrd1, thereby improving cardiac function in AAC rats. Zonisamide can be used in studies of seizure, parkinson’s disease and cardiac hypertrophy. | ||||||||||||||||||||
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Zonisamide-15N,d4 | Zonisamide-15N,d4 is the 15N- and deuterium labeled Zonisamide (HY-B0124). Zonisamide (AD 810) is an orally active carbonic anhydrase inhibitor, with Kis of 35.2 and 20.6 nM for hCA II and hCA V, respectively. Zonisamide exerts neuroprotective effects through anti-apoptosis and upregulating MnSOD levels. Zonisamide also increases the expression of Hrd1, thereby improving cardiac function in AAC rats. Zonisamide can be used in studies of seizure, parkinson’s disease and cardiac hypertrophy. | |||||||||||||||||||||
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Zonisamide-d4 | 99.11% | Zonisamide-d4 is the deuterium labeled Zonisamide. Zonisamide (AD 810) is an inhibitor of zinc enzyme carbonic anhydrase (CA), with Kis of 35.2 nM and 20.6 nM for human mitochondrial isozyme hCA II and hCA V, respectively. Zonisamide has antiepileptic activity. Zonisamide can be used for the rsearch for epilepsy, seizures and Parkinson's disease. | ||||||||||||||||||||
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Zonisamide-13C6 | Zonisamide-13C6 (AD 810-13C6) is 13C labeled Zonisamide. Zonisamide (AD 810) is an orally active carbonic anhydrase inhibitor, with Kis of 35.2 and 20.6 nM for hCA II and hCA V, respectively. Zonisamide exerts neuroprotective effects through anti-apoptosis and upregulating MnSOD levels. Zonisamide also increases the expression of Hrd1, thereby improving cardiac function in AAC rats. Zonisamide can be used in studies of seizure, parkinson’s disease and cardiac hypertrophy. | |||||||||||||||||||||
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Zonisamide | 99.95% | Zonisamide (AD 810) is an orally active carbonic anhydrase inhibitor, with Kis of 35.2 and 20.6 nM for hCA II and hCA V, respectively. Zonisamide exerts neuroprotective effects through anti-apoptosis and upregulating MnSOD levels. Zonisamide also increases the expression of Hrd1, thereby improving cardiac function in AAC rats. Zonisamide can be used in studies of seizure, parkinson’s disease and cardiac hypertrophy. | ||||||||||||||||||||
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