Drug Information
| Drug General Information | Top | |||
|---|---|---|---|---|
| Drug ID |
D0WO8W
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| Former ID |
DAP001232
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| Drug Name |
Mepivacaine
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| Synonyms |
Carbocaine; Mepivacaina; Mepivacainum; Mepivicaine; Scandicain; Scandicaine; Scandicane; Arestocaine HCL; Carboplyin Dental; Isocaine HCL; Carbocaine (TN); Carboplyin Dental (TN); D-mepivacaine; DL-Mepivacaine; Mepivacaina [INN-Spanish]; Mepivacaine (INN); Mepivacaine [INN:BAN]; Mepivacainum [INN-Latin]; Polocaine (TN); Polocaine-Mpf; S-Ropivacaine Mesylate; D(-)-Mepivacaine; N-Methyl-2-pipecolic acid, 2,6-dimethylanilide; N-Methyl-2-pipecolic acid, 2,6-xylidide; N-Methylhexahydro-2-picolinic acid, 2,6-dimethylanilide; N-(2,6-Dimethylphenyl)-1-methyl-2-piperidinecarboxamide; N-(2,6-Dimethylphenyl)-1-methylpiperidine-2-carboxamide; (+-)-1-Methyl-2',6'-pipecoloxylidide; 1-METHYL-2',6'-PIPECOLOXYLIDIDE
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| Drug Type |
Small molecular drug
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| Indication | Analgesia [ICD-11: MB40.8; ICD-10: R20.0] | Approved | [1] | |
| Therapeutic Class |
Anesthetics
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| Company |
Eastman Kodak Co
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| Structure |
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Download2D MOL |
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| Formula |
C15H22N2O
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| Canonical SMILES |
CC1=C(C(=CC=C1)C)NC(=O)C2CCCCN2C
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| 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)
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| InChIKey |
INWLQCZOYSRPNW-UHFFFAOYSA-N
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| CAS Number |
CAS 96-88-8
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| PubChem Compound ID | ||||
| PubChem Substance ID |
9731, 4359672, 7980449, 8152548, 10538842, 11342145, 11362328, 11364374, 11366936, 11369498, 11372616, 11374231, 11377660, 11485547, 11487730, 11489472, 11491444, 11492411, 11495294, 14749722, 29223173, 46507857, 47434354, 48104693, 48416218, 50010838, 50010839, 50105245, 57322122, 80543619, 85171688, 85286140, 85788509, 92714299, 92729954, 96024871, 103301299, 104305320, 124883611, 124883612, 125345418, 126629593, 126655513, 128194970, 131306159, 134338471, 134972696, 135075239, 137102099, 137187317
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| ChEBI ID |
CHEBI:6759
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| ADReCS Drug ID | BADD_D01387 ; BADD_D01388 | |||
| SuperDrug ATC ID |
N01BB03
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| SuperDrug CAS ID |
cas=000096888
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| Target and Pathway | Top | |||
|---|---|---|---|---|
| Target(s) | Sodium channel unspecific (NaC) | Target Info | Blocker | [2] |
| KEGG Pathway | Dopaminergic synapse | |||
| Reactome | Interaction between L1 and Ankyrins | |||
| References | Top | |||
|---|---|---|---|---|
| REF 1 | Drugs@FDA. U.S. Food and Drug Administration. U.S. Department of Health & Human Services. 2015 | |||
| REF 2 | Block of neuronal tetrodotoxin-resistant Na+ currents by stereoisomers of piperidine local anesthetics. Anesth Analg. 2000 Dec;91(6):1499-505. | |||
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