| Stem definition | Drug id | CAS RN |
|---|---|---|
| opioid receptor antagonists/agonists, morphinan derivates | 454 | 42408-82-2 |
| Dose | Unit | Route |
|---|---|---|
| 12 | mg | P |
| Property | Value | Reference |
|---|---|---|
| BDDCS (Biopharmaceutical Drug Disposition Classification System) | 1 | Benet LZ, Broccatelli F, Oprea TI |
| S (Water solubility) | 2 mg/mL | Benet LZ, Broccatelli F, Oprea TI |
| EoM (Fraction excreted unchanged in urine) | 2 % | Benet LZ, Broccatelli F, Oprea TI |
| MRTD (Maximum Recommended Therapeutic Daily Dose) | 0.82 ยตM/kg/day | Contrera JF, Matthews EJ, Kruhlak NL, Benz RD |
| BA (Bioavailability) | 17 % | Kim MT, Sedykh A, Chakravarti SK, Saiakhov RD, Zhu H |
| Vd (Volume of distribution) | 12 L/kg | Lombardo F, Berellini G, Obach RS |
| CL (Clearance) | 41 mL/min/kg | Lombardo F, Berellini G, Obach RS |
| fu (Fraction unbound in plasma) | 0.17 % | Lombardo F, Berellini G, Obach RS |
| t_half (Half-life) | 4.80 hours | Lombardo F, Berellini G, Obach RS |
| Date | Agency | Company | Orphan |
|---|---|---|---|
| Aug. 22, 1978 | FDA |
| MedDRA adverse event term | Likelihood ratio | Likelihood ratio threshold | Patients taking drug having adverse event | Patients taking drug not having adverse event | Patients not taking drug having adverse event | Patients not taking drug not having adverse event |
|---|---|---|---|---|---|---|
| Drug hypersensitivity | 287.78 | 32.64 | 103 | 433 | 310584 | 63177902 |
None
| MedDRA adverse event term | Likelihood ratio | Likelihood ratio threshold | Patients taking drug having adverse event | Patients taking drug not having adverse event | Patients not taking drug having adverse event | Patients not taking drug not having adverse event |
|---|---|---|---|---|---|---|
| Drug hypersensitivity | 276.03 | 36.24 | 87 | 320 | 298829 | 79445152 |
| Treatment failure | 37.77 | 36.24 | 18 | 389 | 170468 | 79573513 |
None
| Source | Code | Description |
|---|---|---|
| ATC | N02AF01 | NERVOUS SYSTEM ANALGESICS OPIOIDS Morphinan derivatives |
| CHEBI has role | CHEBI:35482 | narcotic analgesic |
| CHEBI has role | CHEBI:51177 | anti-tussive |
| CHEBI has role | CHEBI:55322 | mu-opioid agonists |
| CHEBI has role | CHEBI:59282 | kappa-opioid receptor agonists |
| MeSH PA | D000700 | Analgesics |
| MeSH PA | D000701 | Analgesics, Opioid |
| MeSH PA | D000996 | Antitussive Agents |
| MeSH PA | D002491 | Central Nervous System Agents |
| MeSH PA | D002492 | Central Nervous System Depressants |
| MeSH PA | D009292 | Narcotic Antagonists |
| MeSH PA | D009294 | Narcotics |
| MeSH PA | D018373 | Peripheral Nervous System Agents |
| MeSH PA | D019141 | Respiratory System Agents |
| MeSH PA | D018689 | Sensory System Agents |
| FDA MoA | N0000175685 | Partial Opioid Agonists |
| FDA MoA | N0000175686 | Competitive Opioid Antagonists |
| FDA EPC | N0000175692 | Opioid Agonist/Antagonist |
| Disease | Relation | SNOMED_ID | DOID |
|---|---|---|---|
| Pain | indication | 22253000 | |
| General anesthesia | indication | 50697003 | |
| Labor pain | indication | 247412007 | |
| Sedation as Adjunct to Anesthesia | indication | ||
| Migraine | off-label use | 37796009 | DOID:6364 |
| Chronic disease of respiratory system | contraindication | 17097001 | |
| Myocardial infarction | contraindication | 22298006 | DOID:5844 |
| Chronic heart failure | contraindication | 48447003 | |
| Substance abuse | contraindication | 66214007 | |
| Benign intracranial hypertension | contraindication | 68267002 | DOID:11459 |
| Opioid dependence | contraindication | 75544000 | DOID:2559 |
| Decreased respiratory function | contraindication | 80954004 | |
| Injury of head | contraindication | 82271004 | |
| Impaired renal function disorder | contraindication | 197663003 | |
| Disease of liver | contraindication | 235856003 | DOID:409 |
| Disorder of coronary artery | contraindication | 414024009 |
| Species | Use | Relation |
|---|---|---|
| Cats | Pain caused by major or minor trauma | Indication |
| Cats | Pain associated with surgical procedures | Indication |
| Dogs | Chronic nonproductive cough associated with tracheo-bronchitis, tracheitis tonsillitis | Indication |
| Dogs | Laryngitis and pharyngitis associated with inflammatory conditions of the upper respiratory tract | Indication |
| Horses | Pain associated with colic and postpartum pain | Indication |
| Product | Applicant | Ingredients |
|---|---|---|
| Torbutrol Injection | Zoetis Inc. | 1 |
| Torbutrol Tablets | Zoetis Inc. | 1 |
| Torbugesic | Zoetis Inc. | 1 |
| Torbugesic-SA | Zoetis Inc. | 1 |
| Dolorex | Intervet Inc. | 1 |
| Butorphanol Tartrate Injection | Dechra Veterinary Products LLC | 1 |
| Butorphic Injection | Akorn Animal Health Inc. | 1 |
| Butorphanol Tartrate Injection | Dechra Veterinary Products LLC | 1 |
| Dissociation level | Dissociation constant | Type (acidic/basic) |
|---|---|---|
| pKa1 | 9.7 | acidic |
| pKa2 | 8.56 | Basic |
None
None
| Target | Class | Pharos | UniProt | Action | Type | Activity value (-log[M]) | Mechanism action | Bioact source | MoA source |
|---|---|---|---|---|---|---|---|---|---|
| Mu-type opioid receptor | GPCR | PARTIAL AGONIST | Ki | 9.92 | CHEMBL | CHEMBL | |||
| Kappa-type opioid receptor | GPCR | PARTIAL AGONIST | Ki | 9.92 | CHEMBL | CHEMBL | |||
| Delta-type opioid receptor | GPCR | Ki | 7.92 | CHEMBL |
| ID | Source |
|---|---|
| 4019650 | VUID |
| N0000147743 | NUI |
| D00837 | KEGG_DRUG |
| 58786-99-5 | SECONDARY_CAS_RN |
| 1841 | RXNORM |
| C0006491 | UMLSCUI |
| CHEBI:3242 | CHEBI |
| CHEMBL33986 | ChEMBL_ID |
| DB00611 | DRUGBANK_ID |
| CHEMBL299400 | ChEMBL_ID |
| D002077 | MESH_DESCRIPTOR_UI |
| 5361092 | PUBCHEM_CID |
| 7591 | IUPHAR_LIGAND_ID |
| 3620 | INN_ID |
| QV897JC36D | UNII |
| 11596 | MMSL |
| 4315 | MMSL |
| d00838 | MMSL |
| 13936006 | SNOMEDCT_US |
| 373467000 | SNOMEDCT_US |
| 69241001 | SNOMEDCT_US |
| 4018146 | VANDF |
| 4019650 | VANDF |
| 001580 | NDDF |
| 004635 | NDDF |
| Product | Category | Ingredients | NDC | Form | Quantity | Route | Marketing | Label |
|---|---|---|---|---|---|---|---|---|
| Butorphanol Tartrate | HUMAN PRESCRIPTION DRUG LABEL | 1 | 0054-3090 | SPRAY, METERED | 10 mg | NASAL | ANDA | 29 sections |
| Butorphanol Tartrate | HUMAN PRESCRIPTION DRUG LABEL | 1 | 0054-3090 | SPRAY, METERED | 10 mg | NASAL | ANDA | 29 sections |
| Butorphanol Tartrate | HUMAN PRESCRIPTION DRUG LABEL | 1 | 0143-9864 | INJECTION, SOLUTION | 1 mg | INTRAMUSCULAR | ANDA | 28 sections |
| Butorphanol Tartrate | HUMAN PRESCRIPTION DRUG LABEL | 1 | 0143-9867 | INJECTION, SOLUTION | 2 mg | INTRAMUSCULAR | ANDA | 28 sections |
| Butorphanol Tartrate | HUMAN PRESCRIPTION DRUG LABEL | 1 | 0409-1623 | INJECTION, SOLUTION | 1 mg | INTRAMUSCULAR | ANDA | 31 sections |
| Butorphanol Tartrate | HUMAN PRESCRIPTION DRUG LABEL | 1 | 0409-1623 | INJECTION, SOLUTION | 1 mg | INTRAMUSCULAR | ANDA | 31 sections |
| Butorphanol Tartrate | HUMAN PRESCRIPTION DRUG LABEL | 1 | 0409-1623 | INJECTION, SOLUTION | 1 mg | INTRAMUSCULAR | ANDA | 31 sections |
| Butorphanol Tartrate | HUMAN PRESCRIPTION DRUG LABEL | 1 | 0409-1626 | INJECTION, SOLUTION | 2 mg | INTRAMUSCULAR | ANDA | 31 sections |
| Butorphanol Tartrate | HUMAN PRESCRIPTION DRUG LABEL | 1 | 0409-1626 | INJECTION, SOLUTION | 2 mg | INTRAMUSCULAR | ANDA | 31 sections |
| Butorphanol Tartrate | HUMAN PRESCRIPTION DRUG LABEL | 1 | 0409-1626 | INJECTION, SOLUTION | 2 mg | INTRAMUSCULAR | ANDA | 31 sections |
| Butorphanol Tartrate | HUMAN PRESCRIPTION DRUG LABEL | 1 | 60505-0813 | SPRAY | 10 mg | NASAL | ANDA | 15 sections |
| Butorphanol Tartrate | HUMAN PRESCRIPTION DRUG LABEL | 1 | 60505-0813 | SPRAY | 10 mg | NASAL | ANDA | 15 sections |