4-Hydroxy Mepivacaine D3

Product Name 4-Hydroxy Mepivacaine D3
Alternate Names Mepivacaine Stable Isotopes, Stable Isotopes of Mepivacaine
CAT No. CS-T-55809
CAS No. 1323251-06-4
Category Stable Isotopes
Stock Enquire
Mol. Wt. Not Available
Mol. For. Not Available
Hazardous This is not a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Mepivacaine
Canonical Smiles CC1=CC(=CC(=C1NC(=O)C2CCCCN2C)C)O
InchIKey FBFWYQLEUFLRTK-HPRDVNIFSA-N
Inchl InChI=1S/C15H22N2O2/c1-10-8-12(18)9-11(2)14(10)16-15(19)13-6-4-5-7-17(13)3/h8-9,13,18H,4-7H2,1-3H3,(H,16,19)/i3D3
IUPAC N-(4-hydroxy-2,6-dimethylphenyl)-1-(trideuteriomethyl)piperidine-2-carboxamide
Controlled No
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4-Hydroxy Mepivacaine D3 is a synthetic local anesthetic drug that belongs to the amino amide group. It is an isotopically labeled version of the drug, Mepivacaine, which is commonly used in dental procedures and minor surgical interventions. The D3 suffix indicates that the drug contains three deuterium atoms, which are isotopes of hydrogen. The primary use of 4-Hydroxy Mepivacaine D3 is in medical research, particularly in pharmacokinetic and pharmacodynamic studies. The isotopic labeling allows researchers to track the drug's metabolism and distribution in the body, which is useful in determining its efficacy and potential toxicity. The drug's properties also make it a useful tool in studying drug interactions and drug-drug interactions. The chemical structure of 4-Hydroxy Mepivacaine D3 consists of a piperidine ring, a tertiary amine group, and an aromatic ring. The hydroxy group can undergo conjugation with glucuronic acid, which facilitates its elimination from the body. The drug's mechanism of action involves blocking the sodium channels in nerve fibers, which prevents the transmission of pain signals to the brain. In summary, 4-Hydroxy Mepivacaine D3 is a synthetic local anesthetic drug that is primarily used in medical research. Its isotopic labeling allows researchers to study its pharmacokinetics and pharmacodynamics, making it a valuable tool in drug development and testing. The drug's mechanism of action involves blocking sodium channels in nerve fibers, which is effective in reducing pain.

Related Compounds

N-Methyl Mepivacaine-d6 | Mepivacaine-d3 N-Oxide | Mepivacaine-d3 |

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