Methocarbamol
A centrally acting muscle relaxant used to relieve pain and spasms associated with acute musculoskeletal conditions, typically as an adjunct to rest and physical therapy. It works by depressing the central nervous system.
الوزن الجزيئي
241,2400 g/mol
LogP
0,60
TPSA
91,00 Ų
قاعدة ليبينسكي للخمسة
ناجح
المجالات العلاجية
آلية العمل
Reduces skeletal muscle tone and spasm through central or peripheral mechanisms, typically by modulating spinal reflexes, enhancing inhibitory neurotransmission, or blocking neuromuscular transmission.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Reduces skeletal muscle tone and spasm through central or peripheral mechanisms, typically by modulating spinal reflexes, enhancing inhibitory neurotransmission, or blocking neuromuscular transmission.
البنية ثنائية الأبعاد
Cite this structure
Embed this structure
SMILES
COc1ccccc1OCC(O)COC(N)=O
InChI
InChI=1S/C11H15NO5/c1-15-9-4-2-3-5-10(9)16-6-8(13)7-17-11(12)14/h2-5,8,13H,6-7H2,1H3,(H2,12,14)
Molecular Formula
C11H15NO5
HBD / HBA
2 / 5
الروابط القابلة للدوران
7
الذرات الثقيلة
17
No targets recorded
Target interaction data is not yet available for this drug.
No interactions recorded
Drug interaction data is not yet available for this compound.
No side effects recorded
Side effect data is not yet available for this drug.
الأسئلة الشائعة
A centrally acting muscle relaxant used to relieve pain and spasms associated with acute musculoskeletal conditions, typically as an adjunct to rest and physical therapy. It works by depressing the central nervous system.
Reduces skeletal muscle tone and spasm through central or peripheral mechanisms, typically by modulating spinal reflexes, enhancing inhibitory neurotransmission, or blocking neuromuscular transmission.
Yes, Methocarbamol is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL1201117. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 4107. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.
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