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[Lidocaine] >[Lidocaine] CAS number /137-58-6 ATC code /N01 BB02 C01 BB01 D04 AB01 S02 DA01 C05 AD01 PubChem /3676 DrugBank /APRD00479 Formula /C 14 H 22 N 2 O Mol. mass /234.34 g/mol Bioavailability /35% (oral) 3% (topical) Metabolism /Hepatic , 90% CYP1A2 -mediatedExcretion /renal Pregnancy cat. /
A(AU ) Legal status /
Prescription Only (S4) (AU ) Routes /IV , subcutaneous , topical
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Lidocaine ¿¡ ´ëÇÑ µ¶¼ºÁ¤º¸ : Á¤º¸º¸±â
Ãâó: ±¹¸³µ¶¼º°úÇпø µ¶¼º¹°ÁúÁ¤º¸DB : http://www.nitr.go.kr/nitr/contents/m134200/view.do
Mechanism of Action
Lidocaine¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Lidocaine stabilizes the neuronal membrane by inhibiting the ionic fluxes required for the initiation and conduction of impulses thereby effecting local anesthetic action.
Pharmacology
Lidocaine¿¡ ´ëÇÑ Pharmacology Á¤º¸ Lidocaine is an anesthetic agent indicated for production of local or regional anesthesia and in the treatment of ventricular tachycardia occurring during cardiac manipulation, such as surgery or catheterization, or which may occur during acute myocardial infarction, digitalis toxicity, or other cardiac diseases. The mode of action of the antiarrhythmic effect of Lidocaine appears to be similar to that of procaine, procainamide and quinidine. Ventricular excitability is depressed and the stimulation threshold of the ventricle is increased during diastole. The sinoatrial node is, however, unaffected. In contrast to the latter 3 drugs, Lidocaine in therapeutic doses does not produce a significant decrease in arterial pressure or in cardiac contractile force. In larger doses, lidocaine may produce circulatory depression, but the magnitude of the change is less than that found with comparable doses of procainamide.
Metabolism
Lidocaine¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Cytochrome P450 1A2 (CYP1A2)Cytochrome P450 2D6 (CYP2D6)
Absorption
Lidocaine¿¡ ´ëÇÑ Absorption Á¤º¸ Information derived from diverse formulations, concentrations and usages reveals that lidocaine is completely absorbed following parenteral administration, its rate of absorption depending, for example, upon various factors such as the site of administration and the presence or absence of a vasoconstrictor agent.
Toxicity
Lidocaine¿¡ ´ëÇÑ Toxicity Á¤º¸ The oral LD 50 of lidocaine HCl in non-fasted female rats is 459 (346-773) mg/kg (as the salt) and 214 (159-324) mg/kg (as the salt) in fasted female rats. Symptoms of overdose include convulsions, hypoxia, acidosis, bradycardia, arrhythmias and cardiac arrest.
Drug Interactions
Lidocaine¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Not Available
CYP450 Drug Interaction
[CYP450 TableÁ÷Á¢Á¶È¸]
Food Interaction
Lidocaine¿¡ ´ëÇÑ Food Interaction Á¤º¸ Not Available
Drug Target
[Drug Target]
Description
Lidocaine¿¡ ´ëÇÑ Description Á¤º¸ A local anesthetic and cardiac depressant used as an antiarrhythmia agent. Its actions are more intense and its effects more prolonged than those of procaine but its duration of action is shorter than that of bupivacaine or prilocaine. [PubChem]
Dosage Form
Lidocaine¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Aerosol TopicalAerosol, metered TopicalCream TopicalGel TopicalJelly TopicalJelly UrethralLiquid BuccalLiquid DentalLiquid InfiltrationLiquid IntravenousLiquid OralLiquid TopicalLotion TopicalOintment TopicalSolution InfiltrationSolution IntramuscularSolution IntravenousSolution OralSolution TopicalSpray TopicalSwab Topical
Drug Category
Lidocaine¿¡ ´ëÇÑ Drug_Category Á¤º¸ AnestheticsAnesthetics, LocalAnti-Arrhythmia AgentsAntiarrhythmic Agents
Smiles String Canonical
Lidocaine¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CCN(CC)CC(=O)NC1=C(C)C=CC=C1C
Smiles String Isomeric
Lidocaine¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ CCN(CC)CC(=O)NC1=C(C)C=CC=C1C
InChI Identifier
Lidocaine¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C14H22N2O/c1-5-16(6-2)10-13(17)15-14-11(3)8-7-9-12(14)4/h7-9H,5-6,10H2,1-4H3,(H,15,17)/f/h15H
Chemical IUPAC Name
Lidocaine¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ 2-diethylamino-N-(2,6-dimethylphenyl)acetamide
Drug-Induced Toxicity Related Proteins
DOCA ÀÇ Drug-Induced Toxicity Related ProteinÁ¤º¸Replated Protein :Aquaporin-2Drug :DOCA Toxicity :hypertension. [¹Ù·Î°¡±â] LIDOCAINE ÀÇ Drug-Induced Toxicity Related ProteinÁ¤º¸Replated Protein :glucose-regulated protein Drug :lidocaine Toxicity :intestinal disorder. [¹Ù·Î°¡±â] Replated Protein :Alkaline phosphataseDrug :lidocaine Toxicity :lidocaine induced hepatitis. [¹Ù·Î°¡±â] Replated Protein :C-reactive proteinDrug :lidocaine Toxicity :fever. [¹Ù·Î°¡±â] Replated Protein :C-reactive proteinDrug :lidocaine Toxicity :lidocaine induced hepatitis. [¹Ù·Î°¡±â] Replated Protein :Alpha-1-acid glycoproteinDrug :lidocaine Toxicity :lidocaine tolerance. [¹Ù·Î°¡±â] Replated Protein :Gamma-glutamyltranspeptidase Drug :lidocaine Toxicity :fever. [¹Ù·Î°¡±â] Replated Protein :Alkaline phosphataseDrug :lidocaine Toxicity :fever. [¹Ù·Î°¡±â] Replated Protein :Gamma-glutamyltranspeptidase Drug :lidocaine Toxicity :lidocaine induced hepatitis. [¹Ù·Î°¡±â]
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