| Stem definition | Drug id | CAS RN |
|---|---|---|
| 2172 | 2062-78-4 |
| Dose | Unit | Route |
|---|---|---|
| 4 | mg | O |
| Property | Value | Reference |
|---|---|---|
| BDDCS (Biopharmaceutical Drug Disposition Classification System) | 1 | Benet LZ, Broccatelli F, Oprea TI |
| S (Water solubility) | 0.01 mg/mL | Bocci G, Oprea TI, Benet LZ |
| MRTD (Maximum Recommended Therapeutic Daily Dose) | 0.31 ยตM/kg/day | Contrera JF, Matthews EJ, Kruhlak NL, Benz RD |
| BA (Bioavailability) | 40 % | Kim MT, Sedykh A, Chakravarti SK, Saiakhov RD, Zhu H |
| Date | Agency | Company | Orphan |
|---|---|---|---|
| July 31, 1984 | FDA | TEVA |
| 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 |
|---|---|---|---|---|---|---|
| Congenital central nervous system anomaly | 71.26 | 65.09 | 10 | 541 | 334 | 63488137 |
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 |
|---|---|---|---|---|---|---|
| Neuroleptic malignant syndrome | 84.22 | 48.21 | 24 | 761 | 27535 | 79716068 |
| Parkinsonism | 71.77 | 48.21 | 19 | 766 | 16565 | 79727038 |
| Dystonia | 49.34 | 48.21 | 15 | 770 | 21384 | 79722219 |
None
| Source | Code | Description |
|---|---|---|
| ATC | N05AG02 | NERVOUS SYSTEM PSYCHOLEPTICS ANTIPSYCHOTICS Diphenylbutylpiperidine derivatives |
| MeSH PA | D018726 | Anti-Dyskinesia Agents |
| MeSH PA | D014150 | Antipsychotic Agents |
| MeSH PA | D002491 | Central Nervous System Agents |
| MeSH PA | D002492 | Central Nervous System Depressants |
| MeSH PA | D015259 | Dopamine Agents |
| MeSH PA | D018492 | Dopamine Antagonists |
| MeSH PA | D018377 | Neurotransmitter Agents |
| MeSH PA | D011619 | Psychotropic Drugs |
| MeSH PA | D014149 | Tranquilizing Agents |
| CHEBI has role | CHEBI:37955 | H1 receptor antagonists |
| CHEBI has role | CHEBI:48279 | serotonin antagonists |
| CHEBI has role | CHEBI:48561 | dopaminergic antagonists |
| CHEBI has role | CHEBI:65190 | typical antipsychotic drugs |
| CHEBI has role | CHEBI:66956 | antidyskinetic agent |
| FDA EPC | N0000180182 | Typical Antipsychotic |
| Disease | Relation | SNOMED_ID | DOID |
|---|---|---|---|
| Gilles de la Tourette's syndrome | indication | 5158005 | DOID:11119 |
| Neuroleptic malignant syndrome | contraindication | 15244003 | DOID:14464 |
| Senile dementia | contraindication | 15662003 | |
| Agranulocytosis | contraindication | 17182001 | DOID:12987 |
| Glaucoma | contraindication | 23986001 | DOID:1686 |
| Torsades de pointes | contraindication | 31722008 | |
| Parkinsonism | contraindication | 32798002 | |
| Hypokalemia | contraindication | 43339004 | |
| Conduction disorder of the heart | contraindication | 44808001 | |
| Leukopenia | contraindication | 84828003 | DOID:615 |
| Kidney disease | contraindication | 90708001 | DOID:557 |
| Tardive dyskinesia | contraindication | 102449007 | |
| Prolonged QT interval | contraindication | 111975006 | |
| Seizure disorder | contraindication | 128613002 | |
| Hypomagnesemia | contraindication | 190855004 | |
| Motor tic disorder | contraindication | 230337001 | |
| Disease of liver | contraindication | 235856003 | DOID:409 |
| Hyperprolactinemia | contraindication | 237662005 | DOID:12700 |
| Benign prostatic hyperplasia | contraindication | 266569009 | |
| Retention of urine | contraindication | 267064002 | |
| Neutropenic disorder | contraindication | 303011007 | DOID:1227 |
| Coma | contraindication | 371632003 | |
| Congenital long QT syndrome | contraindication | 442917000 | |
| Carcinoma of female breast | contraindication | 447782002 | |
| Drug Induced CNS Depression | contraindication |
None
None
| Dissociation level | Dissociation constant | Type (acidic/basic) |
|---|---|---|
| pKa1 | 9.93 | acidic |
| pKa2 | 8.42 | Basic |
None
None
| Target | Class | Pharos | UniProt | Action | Type | Activity value (-log[M]) | Mechanism action | Bioact source | MoA source |
|---|---|---|---|---|---|---|---|---|---|
| D(2) dopamine receptor | GPCR | ANTAGONIST | Ki | 8.86 | WOMBAT-PK | CHEMBL | |||
| D(3) dopamine receptor | GPCR | ANTAGONIST | Ki | 9.05 | WOMBAT-PK | ||||
| Histamine H1 receptor | GPCR | Ki | 6.71 | WOMBAT-PK | |||||
| Mu-type opioid receptor | GPCR | IC50 | 6.43 | CHEMBL | |||||
| Alpha-2A adrenergic receptor | GPCR | Ki | 5.80 | PDSP | |||||
| Sigma non-opioid intracellular receptor 1 | Membrane receptor | Ki | 6.84 | WOMBAT-PK | |||||
| Potassium voltage-gated channel subfamily H member 2 | Ion channel | IC50 | 7.75 | WOMBAT-PK | |||||
| Multidrug resistance protein 1 | Transporter | IC50 | 5.54 | WOMBAT-PK | |||||
| 5-hydroxytryptamine receptor 1A | GPCR | Ki | 6.63 | WOMBAT-PK | |||||
| 5-hydroxytryptamine receptor 2A | GPCR | ANTAGONIST | Ki | 7.56 | WOMBAT-PK | ||||
| 5-hydroxytryptamine receptor 2C | GPCR | Ki | 6.06 | PDSP | |||||
| 5-hydroxytryptamine receptor 6 | GPCR | Ki | 7.15 | WOMBAT-PK | |||||
| 5-hydroxytryptamine receptor 7 | GPCR | Ki | 9.30 | WOMBAT-PK | |||||
| Alpha-1A adrenergic receptor | GPCR | Ki | 6.70 | WOMBAT-PK | |||||
| Histamine H4 receptor | GPCR | Ki | 5.70 | CHEMBL | |||||
| Muscarinic acetylcholine receptor M3 | GPCR | Ki | 5.71 | PDSP | |||||
| 5-hydroxytryptamine receptor 1D | GPCR | Ki | 5.51 | PDSP | |||||
| Alpha-2C adrenergic receptor | GPCR | Ki | 6.42 | WOMBAT-PK | |||||
| D(4) dopamine receptor | GPCR | ANTAGONIST | Ki | 8.75 | WOMBAT-PK | ||||
| Kappa-type opioid receptor | GPCR | IC50 | 6 | CHEMBL | |||||
| Multidrug resistance-associated protein 1 | Transporter | IC50 | 6 | WOMBAT-PK | |||||
| Glycine receptor subunit alpha-1 | Ion channel | EC50 | 5.77 | CHEMBL | |||||
| Voltage-dependent T-type calcium channel subunit alpha-1G | Ion channel | Kd | 7.40 | CHEMBL | |||||
| Calmodulin | Cytosolic other | IC50 | 5.22 | WOMBAT-PK | |||||
| Delta-type opioid receptor | GPCR | IC50 | 5.42 | CHEMBL | |||||
| Voltage-dependent T-type calcium channel subunit alpha-1H | Ion channel | BLOCKER | IC50 | 6.80 | IUPHAR | ||||
| Voltage-dependent T-type calcium channel subunit alpha-1I | Ion channel | BLOCKER | IC50 | 7.50 | IUPHAR | ||||
| Potassium channel subfamily K member 2 | Ion channel | IC50 | 5.75 | CHEMBL | |||||
| Potassium voltage-gated channel subfamily A member 10 | Ion channel | BLOCKER | IC50 | 6.50 | IUPHAR | ||||
| Solute carrier family 22 member 2 | Transporter | IC50 | 4.47 | CHEMBL | |||||
| Ubiquitin carboxyl-terminal hydrolase 1 | Enzyme | IC50 | 5.70 | CHEMBL | |||||
| Alpha-2B adrenergic receptor | GPCR | Ki | 6.09 | WOMBAT-PK | |||||
| 5-hydroxytryptamine receptor 7 | GPCR | Ki | 9.30 | CHEMBL | |||||
| Sodium channel protein type 2 subunit alpha | Ion channel | IC50 | 6.47 | CHEMBL | |||||
| D(2) dopamine receptor | GPCR | Ki | 9.22 | CHEMBL | |||||
| 5-hydroxytryptamine receptor 6 | GPCR | ANTAGONIST | Ki | 7.20 | IUPHAR | ||||
| Dopamine receptor | GPCR | IC50 | 9.40 | CHEMBL | |||||
| Voltage-dependent T-type calcium channel subunit alpha-1H | Ion channel | BLOCKER | IC50 | 7.30 | IUPHAR | ||||
| G protein-activated inward rectifier potassium channel 2 | Ion channel | GATING INHIBITOR | EC50 | 5.50 | IUPHAR | ||||
| Voltage-dependent T-type calcium channel subunit alpha-1G | Ion channel | BLOCKER | IC50 | 7.50 | IUPHAR |
| ID | Source |
|---|---|
| 4018479 | VUID |
| N0000146801 | NUI |
| D00560 | KEGG_DRUG |
| 4018479 | VANDF |
| C0031935 | UMLSCUI |
| CHEBI:8212 | CHEBI |
| CHEMBL1423 | ChEMBL_ID |
| D010868 | MESH_DESCRIPTOR_UI |
| DB01100 | DRUGBANK_ID |
| 90 | IUPHAR_LIGAND_ID |
| 2330 | INN_ID |
| 1HIZ4DL86F | UNII |
| 16362 | PUBCHEM_CID |
| 8331 | RXNORM |
| 131104 | MMSL |
| 5301 | MMSL |
| d00898 | MMSL |
| 001492 | NDDF |
| 108438008 | SNOMEDCT_US |
| 386848009 | SNOMEDCT_US |
| 1II | PDB_CHEM_ID |
| Product | Category | Ingredients | NDC | Form | Quantity | Route | Marketing | Label |
|---|---|---|---|---|---|---|---|---|
| Pimozide | HUMAN PRESCRIPTION DRUG LABEL | 1 | 49884-347 | TABLET | 1 mg | ORAL | ANDA | 22 sections |
| Pimozide | HUMAN PRESCRIPTION DRUG LABEL | 1 | 49884-348 | TABLET | 2 mg | ORAL | ANDA | 22 sections |