Mepicaine

CAS: 96-88-8

Ref. 3D-FM142923

Información del producto

• Nombre: Mepicaine
• Sinónimos: N- (2, 6- Dimethylphenyl) - 1- methylpiperidine- 2- carboxamide, (.+-.)-Mepivacaine, 1-Methyl-2',6'-pipecoloxylidide, 1-Methyl-2′,6′-pipecoloxylidide, 2',6'-Pipecoloxylidide, 1-methyl-, 2′,6′-Pipecoloxylidide, 1-methyl-, <span class="text-smallcaps">DL</span>-Mepivacaine, Apf 135, Carbocain, Carbocaine, Carbocaine-V, DL-Mepivacaine, DL-N-methylpipecolinate-2, 6-dimethylanilide, MepiSV, N-(2,6-Dimethylphenyl)-1-methyl-2-piperidinecarboxamide, N-(2,6-Dimethylphenyl)-1-methylpiperidin-2-carboxamid, N-(2,6-Dimethylphenyl)-1-methylpiperidine-2-carboxamide, N-(2,6-dimetilfenil)-1-metilpiperidina-2-carboxamida, Scandicain, Scandicaine, Tevacaine
• CAS: 96-88-8

Descripción

Mepicaine is a local anesthetic that is used to provide epidural anesthesia. It has high energy efficiency and can be used for prolonged periods of time. Mepicaine is also an effective anesthetic agent with a long duration of action. Mepicaine has been shown to have the ability to stop phosphodiesterase activity in the nervous system, which may cause it to be more effective than other anesthetics at blocking pain impulses. In addition, mepivacaine and procaine are two related local anesthetics derived from mepicycline, which are both chemically similar to mepincaine.
Mepivicaine can cause allergic reactions, although they are rare and generally mild. This drug also has adrenergic receptor agonist properties, which means that it stimulates receptors that affect the sympathetic nervous system. An example of this would be adrenaline or noradrenaline production in the body. Acute toxicities of mepivicaine include dizziness

• Marca: Biosynth

Propiedades químicas

• Peso molecular: 246.35 g/mol
• Fórmula: C₁₅H₂₂N₂O
• Pureza: Min. 95%
• Color/Forma: White Powder
• 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)
• Clave InChI: InChIKey=INWLQCZOYSRPNW-UHFFFAOYSA-N
• SMILES: Cc1cccc(C)c1NC(=O)C1CCCCN1C