1346597-90-7
1346597-90-7
Chemical Structure
Mepivacaine-d3
- CAS No.: 1346597-90-7
- Formula:C15H19D3N2O
- Molecular Weight:249.37
IUPAC Name: N-(2,6-dimethylphenyl)-1-(methyl-d3)piperidine-2-carboxamide
InChIKey: INWLQCZOYSRPNW-HPRDVNIFSA-N
SMILES: O=C(C1N(CCCC1)C([2H])([2H])[2H])NC2=C(C=CC=C2C)C
Biological Activity: Mepivacaine-d3 is the deuterium labeled Mepivacaine. Mepivacaine is an amide-type local anesthetic agent. Mepivacaine binds to specific voltage-gated sodium ion channels in neuronal cell membranes, which inhibits both sodium influx and membrane depolarization[1][2].
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Mepivacaine-d3 | 99.0% | Mepivacaine-d3 is the deuterium labeled Mepivacaine. Mepivacaine is an amide-type local anesthetic agent. Mepivacaine binds to specific voltage-gated sodium ion channels in neuronal cell membranes, which inhibits both sodium influx and membrane depolarization. | ||||||||||||||||||||
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Mepivacaine hydrochloride (Standard) | ≥98% | Mepivacaine (hydrochloride) (Standard) is the analytical standard of Mepivacaine (hydrochloride). This product is intended for research and analytical applications. Mepivacaine hydrochloride binds to specific voltage-gated sodium ion channels in neuronal cell membranes, which inhibits both sodium influx and membrane depolarization. | ||||||||||||||||||||
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Mepivacaine hydrochloride | 99.68% | Mepivacaine hydrochloride binds to specific voltage-gated sodium ion channels in neuronal cell membranes, which inhibits both sodium influx and membrane depolarization. | ||||||||||||||||||||
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References
- [1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53(2):211-216. [Content Brief]
- [2]. Froehle M, et al. ECMO for Cardiac Rescue after Accidental Intravenous Mepivacaine Application. Case Rep Pediatr. 2012;2012:491692. [Content Brief]
