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Mepivacaine
- русский язык имя
- английское имяMepivacaine
- CAS №22801-44-1
- CBNumberCB8460318
- ФормулаC15H22N2O
- мольный вес246.35
- EINECS1312995-182-4
- номер MDLMFCD00243006
- файл Mol22801-44-1.mol
химическое свойство
Температура плавления | 147-151°C |
температура хранения | -20°C Freezer |
растворимость | Chloroform (Slightly), DMSO (Slightly), Ethanol (Slightly), Methanol (Slightly) |
форма | Solid |
пка | pKa 7.73(H2O,t =25±0.2,I=0.01(NaCl)) (Uncertain) |
цвет | White to Off-White |
InChI | InChI=1S/C15H22N2O/c1-11-7-6-8-12(2)14(11)16-15(18)13-9-4-5-10-17(13)3/h6-8,13H,4-5,9-10H2,1-3H3,(H,16,18) |
ИнЧИКей | INWLQCZOYSRPNW-UHFFFAOYSA-N |
SMILES | N1(C)CCCCC1C(NC1=C(C)C=CC=C1C)=O |
Справочник по базе данных CAS | 22801-44-1(CAS DataBase Reference) |
FDA UNII | B6E06QE59J |
Код УВД | N01BB03,N01BB53 |
Система регистрации веществ EPA | 2-Piperidinecarboxamide, N-(2,6-dimethylphenyl)-1-methyl- (22801-44-1) |
Mepivacaine химические свойства, назначение, производство
Использование
Local anesthetic.Общее описание
Mepivacaine hydrochloride is available in 1% to 3% solutionsand is indicated for infiltration anesthesia, dental procedures,peripheral nerve block, or epidural block. The onset of anesthesiais rapid, ranging from about 3 to 20 minutes for sensoryblock. Mepivacaine is rapidly metabolized in the liver with50% of the administered dose excreted into the bile asmetabolites. The metabolites are reabsorbed in the intestineand excreted in the kidney with only a small percentage foundin the feces. Less than 5% to 10% of the administered dose isfound unchanged in the urine. The primary metabolic productsare the N-demethylated metabolite and the 3 and 4 phenolicmetabolites excreted as their glucuronide conjugates.Клиническое использование
Mepivacaine hydrochloride [N-(2, 6-dimethylphenyl)-1-methyl 2-piperidinecarboxamide monohydrochloride] is an amino amide-type local anesthetic agent widely used to provide regional analgesia and anesthesia by local infiltration, peripheral nerve block, and epidural and caudal blocks. The pharmacological and toxicological profile of mepivacaine is quite similar to that of lidocaine, except that mepivacaine has a slightly longer duration of action and lacks the vasodilator activity of lidocaine. For this reason, it serves as an alternate choice for lidocaine when addition of epinephrine is not recommended in patients with hypertensive vascular disease.Метаболизм
Mepivacaine undergoes extensive hepatic metabolism catalyzed by CYP1A2, with only a small percentage of the administered dosage (<10%) being excreted unchanged in the urine. The major metabolic biotransformations of mepivacaine are N-dealkylation (to give the N-demethylated compound 2′,6′-pipecoloxylidide) and aromatic hydroxylations. These metabolites are excreted as their corresponding glucuronides.Mepivacaine запасные части и сырье
Mepivacaine поставщик
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