Tolperisone
Identification
- Summary
Tolperisone is a muscle relaxant used to relieve spasticity after stroke in adults.
- Generic Name
- Tolperisone
- DrugBank Accession Number
- DB06264
- Background
Tolperisone is an oral, centrally acting muscle relaxant. Its precise mechanism is not completely understood, though it blocks sodium and calcium channels. It possesses a high affinity for nervous system tissue, reaching highest concentrations in brain stem, spinal cord and peripheral nerves. Based on existing clinical data, Tolperisone is not sedating and does not interact with alcohol.
- Type
- Small Molecule
- Groups
- Investigational
- Structure
- Weight
- Average: 245.366
Monoisotopic: 245.177964365 - Chemical Formula
- C16H23NO
- Synonyms
- Tolperisone
- External IDs
- AV650
- SPH-3047
Pharmacology
- Indication
Investigated for use/treatment in neurologic disorders, spinal cord injuries, muscle spasm, back pain, and multiple sclerosis.
Reduce drug development failure ratesBuild, train, & validate machine-learning modelswith evidence-based and structured datasets.Build, train, & validate predictive machine-learning models with structured datasets.- Associated Conditions
Indication Type Indication Combined Product Details Approval Level Age Group Patient Characteristics Dose Form Symptomatic treatment of Spasticity •••••••••••• ••••• •••• •••••• •••••• - Contraindications & Blackbox Warnings
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- Pharmacodynamics
Not Available
- Mechanism of action
- Not Available
- Absorption
Not Available
- Volume of distribution
Not Available
- Protein binding
Not Available
- Metabolism
- Not Available
- Route of elimination
Not Available
- Half-life
Not Available
- Clearance
Not Available
- Adverse Effects
- Improve decision support & research outcomesWith structured adverse effects data, including: blackbox warnings, adverse reactions, warning & precautions, & incidence rates. View sample adverse effects data in our new Data Library!Improve decision support & research outcomes with our structured adverse effects data.
- Toxicity
Not Available
- Pathways
- Not Available
- Pharmacogenomic Effects/ADRs Browse all" title="About SNP Mediated Effects/ADRs" id="snp-actions-info" class="drug-info-popup" href="javascript:void(0);">
- Not Available
Interactions
- Drug Interactions Learn More" title="About Drug Interactions" id="structured-interactions-info" class="drug-info-popup" href="javascript:void(0);">
- This information should not be interpreted without the help of a healthcare provider. If you believe you are experiencing an interaction, contact a healthcare provider immediately. The absence of an interaction does not necessarily mean no interactions exist.
Drug Interaction Integrate drug-drug
interactions in your software1,2-Benzodiazepine The risk or severity of CNS depression can be increased when Tolperisone is combined with 1,2-Benzodiazepine. Acetazolamide The risk or severity of CNS depression can be increased when Acetazolamide is combined with Tolperisone. Acetophenazine The risk or severity of CNS depression can be increased when Acetophenazine is combined with Tolperisone. Agomelatine The risk or severity of CNS depression can be increased when Tolperisone is combined with Agomelatine. Alfentanil The risk or severity of CNS depression can be increased when Alfentanil is combined with Tolperisone. - Food Interactions
- Not Available
Products
- Drug product information from 10+ global regionsOur datasets provide approved product information including:dosage, form, labeller, route of administration, and marketing period.Access drug product information from over 10 global regions.
- Product Ingredients
Ingredient UNII CAS InChI Key Tolperisone hydrochloride 8Z075K2TIG 3644-61-9 ZBUVYROEHQQAKL-UHFFFAOYSA-N - International/Other Brands
- Musclex / Viveo
Categories
- ATC Codes
- M03BX04 — Tolperisone
- M03BX — Other centrally acting agents
- M03B — MUSCLE RELAXANTS, CENTRALLY ACTING AGENTS
- M03 — MUSCLE RELAXANTS
- M — MUSCULO-SKELETAL SYSTEM
- Drug Categories
- Central Nervous System Agents
- Central Nervous System Depressants
- Cytochrome P-450 CYP1A2 Substrates
- Cytochrome P-450 Substrates
- Ketones
- Muscle Relaxants
- Muscle Relaxants, Centrally Acting Agents
- Musculo-Skeletal System
- Neuromuscular Agents
- Peripheral Nervous System Agents
- Propiophenones
- Pyridines
- Topical Products for Joint and Muscular Pain
- Classification
- Not classified
- Affected organisms
- Not Available
Chemical Identifiers
- UNII
- F5EOM0LD8E
- CAS number
- 728-88-1
- InChI Key
- FSKFPVLPFLJRQB-UHFFFAOYSA-N
- InChI
- InChI=1S/C16H23NO/c1-13-6-8-15(9-7-13)16(18)14(2)12-17-10-4-3-5-11-17/h6-9,14H,3-5,10-12H2,1-2H3
- IUPAC Name
- 2-methyl-1-(4-methylphenyl)-3-(piperidin-1-yl)propan-1-one
- SMILES
- CC(CN1CCCCC1)C(=O)C1=CC=C(C)C=C1
References
- General References
- Not Available
- External Links
- KEGG Drug
- D08617
- ChemSpider
- 5310
- BindingDB
- 442744
- 10639
- ChEBI
- 93835
- ChEMBL
- CHEMBL1076211
- Wikipedia
- Tolperisone
Clinical Trials
- Clinical Trials Learn More" title="About Clinical Trials" id="clinical-trials-info" class="drug-info-popup" href="javascript:void(0);">
Phase Status Purpose Conditions Count 3 Completed Treatment Acute Pain / Back Muscle Spasm / Back pain / Back Spasm Upper Back / Back Strain / Muscle Spasms 1 3 Recruiting Treatment Back Pain Lower Back 1 2 Completed Treatment Acute Pain / Back pain / Back Pain Lower Back / Back Spasm Upper Back / Back Strain / Muscle Cramps / Muscle Spasms 1 2 Terminated Treatment Spasticity, Muscle 2 1 Completed Not Available Healthy Subjects (HS) 2
Pharmacoeconomics
- Manufacturers
- Not Available
- Packagers
- Not Available
- Dosage Forms
Form Route Strength Tablet, film coated Oral 150 MG Tablet, coated Oral 50 mg Tablet, film coated Oral 50 mg Tablet 50 mg - Prices
- Not Available
- Patents
- Not Available
Properties
- State
- Solid
- Experimental Properties
- Not Available
- Predicted Properties
Property Value Source Water Solubility 0.167 mg/mL ALOGPS logP 3.75 ALOGPS logP 3.57 Chemaxon logS -3.2 ALOGPS pKa (Strongest Acidic) 16.51 Chemaxon pKa (Strongest Basic) 8.78 Chemaxon Physiological Charge 1 Chemaxon Hydrogen Acceptor Count 2 Chemaxon Hydrogen Donor Count 0 Chemaxon Polar Surface Area 20.31 Å2 Chemaxon Rotatable Bond Count 4 Chemaxon Refractivity 76.35 m3·mol-1 Chemaxon Polarizability 29.6 Å3 Chemaxon Number of Rings 2 Chemaxon Bioavailability 1 Chemaxon Rule of Five Yes Chemaxon Ghose Filter Yes Chemaxon Veber's Rule Yes Chemaxon MDDR-like Rule No Chemaxon - Predicted ADMET Features
- Not Available
Spectra
- Mass Spec (NIST)
- Not Available
- Spectra
Spectrum Spectrum Type Splash Key Predicted MS/MS Spectrum - 10V, Positive (Annotated) Predicted LC-MS/MS splash10-0002-2490000000-6f1421f18912b13a5afe Predicted MS/MS Spectrum - 10V, Negative (Annotated) Predicted LC-MS/MS splash10-0007-0970000000-0d93d16a74ee80f79956 Predicted MS/MS Spectrum - 20V, Positive (Annotated) Predicted LC-MS/MS splash10-00ke-6920000000-4f9f05c65e7a61b8531f Predicted MS/MS Spectrum - 20V, Negative (Annotated) Predicted LC-MS/MS splash10-0007-1930000000-b6c6200b38186590b6e6 Predicted MS/MS Spectrum - 40V, Positive (Annotated) Predicted LC-MS/MS splash10-0002-9630000000-105142f43f48c7ab6684 Predicted MS/MS Spectrum - 40V, Negative (Annotated) Predicted LC-MS/MS splash10-00kf-9410000000-8a424ff46844c34d1f61 Predicted 1H NMR Spectrum 1D NMR Not Applicable Predicted 13C NMR Spectrum 1D NMR Not Applicable - Chromatographic Properties
Collision Cross Sections (CCS)
Adduct CCS Value (Å2) Source type Source [M-H]- 163.33115 predictedDeepCCS 1.0 (2019) [M+H]+ 165.68913 predictedDeepCCS 1.0 (2019) [M+Na]+ 171.78229 predictedDeepCCS 1.0 (2019)
Enzymes
- Kind
- Protein
- Organism
- Humans
- Pharmacological action
- Unknown
- Actions
- Substrate
- Curator comments
- Data are limited to an in vitro study.
- General Function
- Oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygen
- Specific Function
- Cytochromes P450 are a group of heme-thiolate monooxygenases. In liver microsomes, this enzyme is involved in an NADPH-dependent electron transport pathway. It oxidizes a variety of structurally un...
- Gene Name
- CYP1A2
- Uniprot ID
- P05177
- Uniprot Name
- Cytochrome P450 1A2
- Molecular Weight
- 58293.76 Da
References
- Dalmadi B, Leibinger J, Szeberenyi S, Borbas T, Farkas S, Szombathelyi Z, Tihanyi K: Identification of metabolic pathways involved in the biotransformation of tolperisone by human microsomal enzymes. Drug Metab Dispos. 2003 May;31(5):631-6. [Article]
Drug created at March 19, 2008 16:20 / Updated at June 19, 2021 00:26