Methocarbamol
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Also known as DelaxinForbaxinMethocarbamol component of robaxisalMetocarbamolMiolaxinNSC-170960NeuraxinRobaxinRobaxin-750SID855587SID26747217SID26747218SID56422407SID174006834SID144204005SID170464808C0165027
Summary
Methocarbamol (CHEMBL1201117) is an approved small molecule (ATC M03BA53) targeting CA1; indicated across 2 conditions including cirrhosis of liver.
At a glance
- Status: Approved (max clinical phase 4)
- Modality: Small molecule
- ATC class: M03BA53 (+2 more)
- Targets: 1 (CA1)
- Indications: 2 conditions
- Clinical trials: 9
- Chemistry: 241.24 Da · C11H15NO5
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL1201117 |
| Name | Methocarbamol |
| Type | Small molecule |
| Max phase | 4 |
| FDA approved | yes |
| PubChem CID | 4107 |
| ChEBI | CHEBI:77498 |
| ATC | M03BA53, M03BA03, M03BA73 |
| Molecular formula | C11H15NO5 |
| Molecular weight | 241.24 |
| InChIKey | GNXFOGHNGIVQEH-UHFFFAOYSA-N |
SMILES: COC1=CC=CC=C1OCC(COC(=O)N)O
IUPAC name: [2-hydroxy-3-(2-methoxyphenoxy)propyl] carbamate
ChEBI definition: A carbamate ester that is glycerol in which one of the primary alcohol groups has been converted to its 2-methoxyphenyl ether while the other has been converted to the corresponding carbamate ester.
Also known as: Delaxin, Forbaxin, Methocarbamol, Methocarbamol component of robaxisal, Metocarbamol, Miolaxin, NSC-170960, Neuraxin, Robaxin, Robaxin-750, SID855587, METHOCARBAMOL
Patent coverage: 2,120 distinct patent families (8,216 SureChEMBL compound mentions), from 2 matched compound structure(s). One matched structure accounts for 8,085 (98%) of the total. Mentions count patents naming the compound (not distinct inventions), so promiscuous / reference molecules inflate the mention figure — families are the dedup metric.
Targets
Targets
Primary targets (GtoPdb curated mechanism): the Cancer dependency column is the DepMap CRISPR fitness signal (% of screened cell lines dependent on the target).
| Gene | Target | Action | pAffinity | Cancer dependency | UniProt |
|---|---|---|---|---|---|
| CA1 | carbonic anhydrase 1 | Inhibition | 7.6 | 0% | P00915 |
Broader ChEMBL bioactivity targets: 1 (assay-derived). Sample: Survival motor neuron protein.
Bioactivity
ChEMBL activities: 1 potent at pChembl ≥ 5 of 1 total. Top 30 by potency (10 = 0.1 nM, 6 = 1 µM):
| Target | pChembl | Type | Value | Unit | Activity ID |
|---|---|---|---|---|---|
| SMN1 | 6.1 | Potency | 794.3 | nM | CHEMBL_ACT_3885854 |
Target pathways
Aggregated over 1 target gene(s): CA1.
Top Reactome pathways
12 total, by targets touching each:
| Pathway | Targets | Genes |
|---|---|---|
| Erythrocytes take up carbon dioxide and release oxygen | 1 | CA1 |
| Erythrocytes take up oxygen and release carbon dioxide | 1 | CA1 |
| Cytokine Signaling in Immune system | 1 | CA1 |
| Metabolism | 1 | CA1 |
| Reversible hydration of carbon dioxide | 1 | CA1 |
| O2/CO2 exchange in erythrocytes | 1 | CA1 |
| Immune System | 1 | CA1 |
| Transport of small molecules | 1 | CA1 |
| Interleukin-12 family signaling | 1 | CA1 |
| Signaling by Interleukins | 1 | CA1 |
| Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation | 1 | CA1 |
| Interleukin-12 signaling | 1 | CA1 |
Dominant GO biological processes
| GO term | Targets |
|---|---|
| response to fructose | 1 |
Indications & clinical
Indications
2 indications (0 at ChEMBL trial phase 4). Phase below is the highest clinical-trial phase recorded for this drug against each disease — not the molecule’s overall approval status (that is in the Summary).
| Indication | Trial phase | MONDO | EFO |
|---|---|---|---|
| cirrhosis of liver | 3 | MONDO:0005155 | EFO:0001422 |
1 further indication record had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.
Clinical trials
Total trials: 9.
Phase distribution
| Phase | Trials |
|---|---|
| PHASE4 | 4 |
| PHASE3 | 3 |
| Not specified | 2 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT05076110 | PHASE4 | RECRUITING | Nonopioid Pain Control Regimen After Arthroscopic Hip Procedures |
| NCT05388929 | PHASE4 | ACTIVE_NOT_RECRUITING | Methocarbamol in Ventral and Inguinal HR |
| NCT02432456 | PHASE4 | COMPLETED | Ketamine Infusion Therapy for the Management of Acute Pain in Adult Rib Fracture Patients |
| NCT02665286 | PHASE4 | COMPLETED | Orphenadrine and Methocarbamol for LBP |
| NCT02642874 | PHASE3 | UNKNOWN | Methocarbamol in Treatment of Muscle Cramps in Cirrhotic Patients |
| NCT02831569 | PHASE3 | COMPLETED | Japanese IP-TN Trial |
| NCT05603832 | PHASE3 | COMPLETED | A Phase 3 Study of F14 for Management of Pain Following Total Knee Replacement |
| NCT05100017 | Not specified | ACTIVE_NOT_RECRUITING | Methocarbamol vs Oxybutynin for Management of Pain and Discomfort S/P Ureteroscopy Procedure |
| NCT06659965 | Not specified | COMPLETED | Intravenous Methocarbamol for Acute Pain After Spine Surgery |
Clinical evidence (CIViC)
No CIViC predictive evidence (expected for non-precision-medicine drugs).
Pharmacology
Pharmacogenomics
No CPIC/DPWG dosing guideline or drug-level clinical/variant annotations in PharmGKB for this molecule.
Related molecules
Related molecules
Molecules sharing ≥1 of this drug’s curated primary targets, merged from two biobtree sources and ranked by shared-target count, then clinical phase: ChEMBL clinical-stage candidates (development phase ≥2) and PubChem drug-class bioactivity (approved / known drugs acting on the target). Deduplicated by drug name; the drug’s own salt forms are excluded. Note: for a drug with few primary targets a shared-target match can reflect off-target / promiscuous binding rather than the same therapeutic mechanism — the phase ordering surfaces bona-fide therapeutics first.
69 molecules share ≥1 primary target. Top 60 by shared-target count:
| Molecule | Source | Status | Shared targets |
|---|---|---|---|
| PAZOPANIB | ChEMBL + PubChem | Phase 4 (approved) | CA1 |
| ACETAMINOPHEN | ChEMBL | Phase 4 (approved) | CA1 |
| ACETAZOLAMIDE | ChEMBL | Phase 4 (approved) | CA1 |
| BORTEZOMIB | ChEMBL | Phase 4 (approved) | CA1 |
| BRINZOLAMIDE | ChEMBL | Phase 4 (approved) | CA1 |
| CELECOXIB | ChEMBL | Phase 4 (approved) | CA1 |
| CHLOROTHIAZIDE | ChEMBL | Phase 4 (approved) | CA1 |
| CHLORTHALIDONE | ChEMBL | Phase 4 (approved) | CA1 |
| COUMARIN | ChEMBL | Phase 4 (approved) | CA1 |
| DICHLORPHENAMIDE | ChEMBL | Phase 4 (approved) | CA1 |
| DIFLUNISAL | ChEMBL | Phase 4 (approved) | CA1 |
| DOBUTAMINE | ChEMBL | Phase 4 (approved) | CA1 |
| DORZOLAMIDE | ChEMBL | Phase 4 (approved) | CA1 |
| ETHOXZOLAMIDE | ChEMBL | Phase 4 (approved) | CA1 |
| FAMOTIDINE | ChEMBL | Phase 4 (approved) | CA1 |
| FUROSEMIDE | ChEMBL | Phase 4 (approved) | CA1 |
| HYDROCHLOROTHIAZIDE | ChEMBL | Phase 4 (approved) | CA1 |
| HYDROQUINONE | ChEMBL | Phase 4 (approved) | CA1 |
| IMATINIB | ChEMBL | Phase 4 (approved) | CA1 |
| INDAPAMIDE | ChEMBL | Phase 4 (approved) | CA1 |
| LACOSAMIDE | ChEMBL | Phase 4 (approved) | CA1 |
| LEVETIRACETAM | ChEMBL | Phase 4 (approved) | CA1 |
| MAFENIDE | ChEMBL | Phase 4 (approved) | CA1 |
| METHAZOLAMIDE | ChEMBL | Phase 4 (approved) | CA1 |
| NILOTINIB | ChEMBL | Phase 4 (approved) | CA1 |
| NITROUS ACID | ChEMBL | Phase 4 (approved) | CA1 |
| PHENOL | ChEMBL | Phase 4 (approved) | CA1 |
| PROPOFOL | ChEMBL | Phase 4 (approved) | CA1 |
| SALICYLIC ACID | ChEMBL | Phase 4 (approved) | CA1 |
| SODIUM | ChEMBL | Phase 4 (approved) | CA1 |
| SULFANILAMIDE | ChEMBL | Phase 4 (approved) | CA1 |
| SULFASALAZINE | ChEMBL | Phase 4 (approved) | CA1 |
| SULFUR | ChEMBL | Phase 4 (approved) | CA1 |
| SULPIRIDE | ChEMBL | Phase 4 (approved) | CA1 |
| SULTHIAME | ChEMBL | Phase 4 (approved) | CA1 |
| TANNIC ACID | ChEMBL | Phase 4 (approved) | CA1 |
| TAVABOROLE | ChEMBL | Phase 4 (approved) | CA1 |
| TOPIRAMATE | ChEMBL | Phase 4 (approved) | CA1 |
| TRICHLORMETHIAZIDE | ChEMBL | Phase 4 (approved) | CA1 |
| TRIENTINE | ChEMBL | Phase 4 (approved) | CA1 |
| VALDECOXIB | ChEMBL | Phase 4 (approved) | CA1 |
| VERALIPRIDE | ChEMBL | Phase 4 (approved) | CA1 |
| ZONISAMIDE | ChEMBL | Phase 4 (approved) | CA1 |
| BICARBONATE | ChEMBL | Phase 3 | CA1 |
| CAFFEIC ACID | ChEMBL | Phase 3 | CA1 |
| CURCUMIN | ChEMBL | Phase 3 | CA1 |
| GUAIACOL | ChEMBL | Phase 3 | CA1 |
| P-TOLUENESULFONAMIDE | ChEMBL | Phase 3 | CA1 |
| PRITELIVIR | ChEMBL | Phase 3 | CA1 |
| QUERCETIN | ChEMBL | Phase 3 | CA1 |
| RESVERATROL | ChEMBL | Phase 3 | CA1 |
| SACCHARIN | ChEMBL | Phase 3 | CA1 |
| SPERMIDINE | ChEMBL | Phase 3 | CA1 |
| BENZYLSULFAMIDE | ChEMBL | Phase 2 | CA1 |
| CARZENIDE | ChEMBL | Phase 2 | CA1 |
| COUMAPHOS | ChEMBL | Phase 2 | CA1 |
| DITIOCARB | ChEMBL | Phase 2 | CA1 |
| ELLAGIC ACID | ChEMBL | Phase 2 | CA1 |
| FLAVONE | ChEMBL | Phase 2 | CA1 |
| GALLIC ACID | ChEMBL | Phase 2 | CA1 |
Related Atlas pages
- Genes: CA1
- Diseases: cirrhosis of liver
- Drugs: Pazopanib, Acetaminophen, Acetazolamide, Bortezomib, Brinzolamide, Celecoxib, Chlorothiazide, Chlorthalidone, Dichlorphenamide, Diflunisal, Dobutamine, Dorzolamide, Ethoxzolamide, Famotidine, Furosemide, Hydrochlorothiazide, Hydroquinone, Imatinib, Indapamide, Lacosamide, Levetiracetam, Mafenide, Methazolamide, Nilotinib, Nitrous Acid, Phenol, Propofol, Salicylic Acid, Sodium, Sulfanilamide, Sulfasalazine, Sulfur, Sulpiride, Sulthiame, Tannic Acid, Tavaborole, Topiramate, Trichlormethiazide, Trientine, Valdecoxib, Veralipride, Zonisamide, Caffeic Acid, Curcumin, Guaiacol, P-Toluenesulfonamide, Pritelivir, Quercetin, Resveratrol, Saccharin, Spermidine