Chlorpromazine
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Also known as AminazineChlorpromazinumClorpromazinaEsmindElmarinFenactilJ2.794DLargactilothiazineMegaphenNovomazinaNSC-167745NSC-226514PropapheninSanopronSKF-2601AThorazineWinterminchloropromazineChlorpoamazine
Summary
Chlorpromazine (CHEMBL71) is an approved small-molecule phenothiazine antipsychotic drug (ATC N05AA01) targeting HTR6, HTR7, and HTR1A; indicated across 11 conditions including psychotic disorder and mental disorder.
At a glance
- Status: Approved (max clinical phase 4)
- Modality: Small molecule
- ATC class: N05AA01
- Targets: 15 (HTR6, HTR7, HTR1A…)
- Indications: 11 conditions
- Clinical trials: 17
- Chemistry: 318.9 Da · C17H19ClN2S
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL71 |
| Name | Chlorpromazine |
| Type | Small molecule |
| Max phase | 4 |
| FDA approved | yes |
| PubChem CID | 2726 |
| ChEBI | CHEBI:3647 |
| ATC | N05AA01 |
| Molecular formula | C17H19ClN2S |
| Molecular weight | 318.9 |
| InChIKey | ZPEIMTDSQAKGNT-UHFFFAOYSA-N |
SMILES: CN(C)CCCN1C2=CC=CC=C2SC3=C1C=C(C=C3)Cl
IUPAC name: 3-(2-chlorophenothiazin-10-yl)-N,N-dimethylpropan-1-amine
ChEBI definition: A substituted phenothiazine in which the ring nitrogen at position 10 is attached to C-3 of an N,N-dimethylpropanamine moiety.
Pharmacological roles (ChEBI): phenothiazine antipsychotic drug, antiemetic, dopaminergic antagonist, EC 3.4.21.26 (prolyl oligopeptidase) inhibitor, anticoronaviral agent.
Also known as: Aminazine, Chlorpromazine, Chlorpromazinum, Clorpromazina, Esmind, Elmarin, Fenactil, J2.794D, Largactilothiazine, Megaphen, Novomazina, NSC-167745
Parent form; salt/anhydrous children: CHEMBL1713
Patent coverage: 13,992 distinct patent families (45,827 SureChEMBL compound mentions), from 3 matched compound structure(s). One matched structure accounts for 45,540 (99%) 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 |
|---|---|---|---|---|---|
| HTR6 | 5-HT6 receptor | Inverse agonist | 7.8 | 0.2% | P50406 |
| HTR7 | 5-HT7 receptor | Inverse agonist | 7.6 | 0.8% | P34969 |
| HTR1A | 5-HT1A receptor | Antagonist | 6.2 | 0% | P08908 |
| DRD1 | D1 receptor | Antagonist | 7.1 | 0% | P21728 |
| DRD2 | D2 receptor | Antagonist | 7.6 | 0% | P14416 |
| DRD3 | D3 receptor | Antagonist | 7.5 | 0% | P35462 |
| DRD4 | D4 receptor | Antagonist | 7.8 | 0% | P21917 |
| DRD5 | D5 receptor | Antagonist | 6.9 | 0% | P21918 |
| ADRA2A | α2A-adrenoceptor | Antagonist | 6.6 | 0.1% | P08913 |
| HRH1 | H1 receptor | Antagonist | 8.2 | 0% | P35367 |
| ADRA2B | α2B-adrenoceptor | Antagonist | 8.3 | 0.2% | P18089 |
| ADRA2C | α2C-adrenoceptor | Antagonist | 7.4 | 0% | P18825 |
| TRPC5 | TRPC5 | 0% | Q9UL62 | ||
| HTR2A | 5-HT2A receptor | Inverse agonist | 8.1 | 0% | P28223 |
| Maxi Cl- | |||||
| HTR2C | 5-HT2C receptor | Antagonist | 8.2 | 0% | P28335 |
Broader ChEMBL bioactivity targets: 105 (assay-derived). Sample: Tyrosyl-DNA phosphodiesterase 1, Microtubule-associated protein tau, Survival motor neuron protein, Prelamin-A/C, 4’-phosphopantetheinyl transferase ffp, Thrombopoietin, Ras-related protein Rab-9A, Aldehyde oxidase 1, Pleiotropic ABC efflux transporter of multiple drugs, Muscarinic acetylcholine receptor M4.
Bioactivity
ChEMBL activities: 253 potent at pChembl ≥ 5 of 307 total. Top 30 by potency (10 = 0.1 nM, 6 = 1 µM):
| Target | pChembl | Type | Value | Unit | Activity ID |
|---|---|---|---|---|---|
| P08909 | 9.15 | Ki | 0.7 | nM | CHEMBL_ACT_315933 |
| DRD2 | 9 | IC50 | 1 | nM | CHEMBL_ACT_15186915 |
| DRD2 | 9 | IC50 | 1 | nM | CHEMBL_ACT_15187892 |
| HTR2A | 8.96 | Ki | 1.1 | nM | CHEMBL_ACT_7709903 |
| DRD2 | 8.92 | Ki | 1.2 | nM | CHEMBL_ACT_12074128 |
| P61169 | 8.92 | Ki | 1.2 | nM | CHEMBL_ACT_461839 |
| DRD3 | 8.8 | Ki | 1.58 | nM | CHEMBL_ACT_1925176 |
| P15823 | 8.8 | Ki | 1.58 | nM | CHEMBL_ACT_1925454 |
| P61169 | 8.75 | Ki | 1.77 | nM | CHEMBL_ACT_378876 |
| DRD2 | 8.74 | Ki | 1.8 | nM | CHEMBL_ACT_19098532 |
| DRD2 | 8.74 | Ki | 1.8 | nM | CHEMBL_ACT_19248922 |
| ADRA1D | 8.71 | Ki | 1.96 | nM | CHEMBL_ACT_7705579 |
| HRH1 | 8.71 | Ki | 1.96 | nM | CHEMBL_ACT_7707720 |
| P61169 | 8.7 | Ki | 2.01 | nM | CHEMBL_ACT_611404 |
| P61169 | 8.7 | Ki | 2 | nM | CHEMBL_ACT_935196 |
| P18901 | 8.67 | IC50 | 2.15 | nM | CHEMBL_ACT_704339 |
| P61169 | 8.66 | Ki | 2.19 | nM | CHEMBL_ACT_378877 |
| DRD2 | 8.63 | Ki | 2.34 | nM | CHEMBL_ACT_24412797 |
| HTR2C | 8.56 | Ki | 2.74 | nM | CHEMBL_ACT_7709907 |
| DRD2 | 8.52 | IC50 | 3 | nM | CHEMBL_ACT_18530272 |
| P61169 | 8.52 | Ki | 3 | nM | CHEMBL_ACT_209816 |
| DRD3 | 8.52 | Ki | 3 | nM | CHEMBL_ACT_708505 |
| DRD3 | 8.48 | Ki | 3.31 | nM | CHEMBL_ACT_13876489 |
| DRD3 | 8.48 | Ki | 3.3 | nM | CHEMBL_ACT_13876524 |
| P08909 | 8.48 | Ki | 3.3 | nM | CHEMBL_ACT_611406 |
| P08909 | 8.48 | Ki | 3.31 | nM | CHEMBL_ACT_935198 |
| HTR2A | 8.47 | IC50 | 3.4 | nM | CHEMBL_ACT_13828626 |
| P43140 | 8.46 | Ki | 3.46 | nM | CHEMBL_ACT_7705575 |
| DRD3 | 8.42 | Ki | 3.8 | nM | CHEMBL_ACT_12074122 |
| HTR2A | 8.41 | IC50 | 3.85 | nM | CHEMBL_ACT_7709902 |
Target pathways
Aggregated over 15 target gene(s): HTR6, HTR7, HTR1A, DRD1, DRD2, DRD3, DRD4, DRD5, ADRA2A, HRH1, ADRA2B, ADRA2C, TRPC5, HTR2A, HTR2C.
Top Reactome pathways
27 total, by targets touching each:
| Pathway | Targets | Genes |
|---|---|---|
| Signal Transduction | 8 | ADRA2A, ADRA2B, ADRA2C, HTR1A, HTR2A, HTR2C, HTR6, HTR7 |
| Signaling by GPCR | 8 | ADRA2A, ADRA2B, ADRA2C, HTR1A, HTR2A, HTR2C, HTR6, HTR7 |
| Class A/1 (Rhodopsin-like receptors) | 8 | ADRA2A, ADRA2B, ADRA2C, HTR1A, HTR2A, HTR2C, HTR6, HTR7 |
| Amine ligand-binding receptors | 8 | ADRA2A, ADRA2B, ADRA2C, HTR1A, HTR2A, HTR2C, HTR6, HTR7 |
| GPCR ligand binding | 8 | ADRA2A, ADRA2B, ADRA2C, HTR1A, HTR2A, HTR2C, HTR6, HTR7 |
| GPCR downstream signalling | 7 | ADRA2A, ADRA2B, ADRA2C, HTR2A, HTR2C, HTR6, HTR7 |
| Dopamine receptors | 5 | DRD1, DRD2, DRD3, DRD4, DRD5 |
| Serotonin receptors | 5 | HTR1A, HTR2A, HTR2C, HTR6, HTR7 |
| G alpha (i) signalling events | 5 | ADRA2A, ADRA2B, ADRA2C, DRD3, DRD4 |
| G alpha (s) signalling events | 4 | DRD1, DRD5, HTR6, HTR7 |
| Hemostasis | 3 | ADRA2A, ADRA2B, ADRA2C |
| Adrenoceptors | 3 | ADRA2A, ADRA2B, ADRA2C |
| Adrenaline signalling through Alpha-2 adrenergic receptor | 3 | ADRA2A, ADRA2B, ADRA2C |
| G alpha (q) signalling events | 3 | HRH1, HTR2A, HTR2C |
| G alpha (z) signalling events | 3 | ADRA2A, ADRA2B, ADRA2C |
| Platelet activation, signaling and aggregation | 3 | ADRA2A, ADRA2B, ADRA2C |
| Platelet Aggregation (Plug Formation) | 3 | ADRA2A, ADRA2B, ADRA2C |
| Metabolism | 2 | ADRA2A, ADRA2C |
| Integration of energy metabolism | 2 | ADRA2A, ADRA2C |
| Metabolism of proteins | 2 | ADRA2A, ADRA2C |
| Adrenaline,noradrenaline inhibits insulin secretion | 2 | ADRA2A, ADRA2C |
| Regulation of insulin secretion | 2 | ADRA2A, ADRA2C |
| Surfactant metabolism | 2 | ADRA2A, ADRA2C |
| TRP channels | 1 | TRPC5 |
| Histamine receptors | 1 | HRH1 |
| Role of second messengers in netrin-1 signaling | 1 | TRPC5 |
| RHOBTB3 ATPase cycle | 1 | HTR7 |
Dominant GO biological processes
| GO term | Targets |
|---|---|
| signal transduction | 14 |
| G protein-coupled receptor signaling pathway | 14 |
| G protein-coupled receptor signaling pathway, coupled to cyclic nucleotide second messenger | 8 |
| chemical synaptic transmission | 8 |
| G protein-coupled serotonin receptor signaling pathway | 6 |
| positive regulation of MAPK cascade | 6 |
| intracellular calcium ion homeostasis | 6 |
| behavioral response to cocaine | 5 |
| phospholipase C-activating dopamine receptor signaling pathway | 5 |
| synaptic transmission, dopaminergic | 5 |
| response to cocaine | 5 |
| adenylate cyclase-modulating G protein-coupled receptor signaling pathway | 4 |
| behavioral fear response | 4 |
| positive regulation of cell population proliferation | 4 |
| regulation of vasoconstriction | 4 |
Indications & clinical
Indications
11 indications (6 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 |
|---|---|---|---|
| psychotic disorder | 4 | MONDO:0005485 | EFO:0005407 |
| mental disorder | 4 | MONDO:0005084 | EFO:0000677 |
| conduct disorder | 4 | MONDO:0005352 | EFO:0004216 |
| porphyria | 4 | MONDO:0037939 | MONDO:0037939 |
| neonatal abstinence syndrome | 3 | MONDO:0005566 | EFO:0005799 |
| severe acute respiratory syndrome | 3 | MONDO:0005091 | MONDO:0100096 |
| delirium | 2 | MONDO:0045057 | EFO:0009267 |
| glioblastoma | 2 | MONDO:0018177 | EFO:0000519 |
| colonic neoplasm | 1 | MONDO:0005401 | MONDO:0021063 |
2 further indication records had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.
Clinical trials
Total trials: 17.
Phase distribution
| Phase | Trials |
|---|---|
| PHASE4 | 4 |
| PHASE3 | 3 |
| PHASE2/PHASE3 | 3 |
| Not specified | 3 |
| PHASE1 | 2 |
| PHASE2 | 1 |
| PHASE1/PHASE2 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT00169039 | PHASE4 | TERMINATED | Clozapine Versus Chlorpromazine for Treatment-Unresponsive Schizophrenia |
| NCT00202293 | PHASE4 | COMPLETED | Comparison of Combination Olanzapine+Lithium or Chlorpromazine+Lithium in Treatment of First Manic Episode With Psychotic Features |
| NCT00654576 | PHASE4 | COMPLETED | Effectiveness of Antipsychotic Combination With Psychosocial Intervention on Outcome of Patients With Schizophrenia |
| NCT03639558 | PHASE4 | COMPLETED | TREC-Lebanon: A Trial for Rapid Tranquilisation for Agitated Patients in the Emergency Setting |
| NCT03021486 | PHASE2/PHASE3 | ACTIVE_NOT_RECRUITING | Haloperidol With or Without Chlorpromazine in Treating Delirium in Patients With Advanced, Metastatic, or Recurrent Cancer |
| NCT05431595 | PHASE2/PHASE3 | RECRUITING | Managing Agitated Delirium With Neuroleptics and Anti-Epileptics as a Neuroleptic Sparing Strategy |
| NCT00882518 | PHASE3 | COMPLETED | Efficacy and Safety of Quetiapine Fumarate in the Treatment of Schizophrenic Patients |
| NCT02810782 | PHASE3 | COMPLETED | How to Treat Opiate Withdrawal in Neonates |
| NCT04354805 | PHASE2/PHASE3 | UNKNOWN | Administration of Chlorpromazine as a Treatment for COVID-19 |
| NCT04366739 | PHASE3 | WITHDRAWN | Repurposing of Chlorpromazine in Covid-19 Treatment |
| NCT04224441 | PHASE2 | UNKNOWN | Repurposing Chlorpromazine in the Treatment of Glioblastoma |
| NCT05433402 | PHASE1/PHASE2 | WITHDRAWN | Repurposing the Antipsychotic Drug Chlorpromazine as Adjuvant Therapeutic Agent for Resected Stage III Colon Cancer |
| NCT06663631 | PHASE1 | RECRUITING | Study on Hibernation-like Therapy Based on Mechanical Thrombectomy |
| NCT05190315 | PHASE1 | COMPLETED | Chlorpromazine and Standard of Care in Glioblastoma |
| NCT01404364 | Not specified | COMPLETED | Use of Intravitreal Triamcinolone and Retrobulbar Chlorpromazine as Alternatives to the Management of Painful Blind Eye |
| NCT02600741 | Not specified | COMPLETED | Family Intervention in Recent Onset Schizophrenia Treatment (FIRST) |
| NCT03183310 | Not specified | UNKNOWN | The Effect of Chlorpromazine on Esophageal Sensitivity in Healthy Volunteers. |
Clinical evidence (CIViC)
No CIViC predictive evidence (expected for non-precision-medicine drugs).
Pharmacology
Pharmacogenomics
No CPIC/DPWG dosing guideline, but PharmGKB curates 1 clinical and 5 variant annotation(s) for this drug (gene-keyed; see PharmGKB).
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.
986 molecules share ≥1 primary target. Top 60 by shared-target count:
| Molecule | Source | Status | Shared targets |
|---|---|---|---|
| BREXPIPRAZOLE | ChEMBL + PubChem | Phase 4 (approved) | ADRA2A, ADRA2B, ADRA2C, DRD1, DRD2, DRD3, DRD4, DRD5, HRH1, HTR1A, HTR2A, HTR2C, HTR6, HTR7 |
| CLOZAPINE | ChEMBL + PubChem | Phase 4 (approved) | ADRA2A, ADRA2B, ADRA2C, DRD1, DRD2, DRD3, DRD4, DRD5, HRH1, HTR1A, HTR2A, HTR2C, HTR6, HTR7 |
| DIHYDROERGOTAMINE | ChEMBL + PubChem | Phase 4 (approved) | ADRA2A, ADRA2B, ADRA2C, DRD1, DRD2, DRD3, DRD4, DRD5, HRH1, HTR1A, HTR2A, HTR2C, HTR6, HTR7 |
| OLANZAPINE | ChEMBL + PubChem | Phase 4 (approved) | ADRA2A, ADRA2B, ADRA2C, DRD1, DRD2, DRD3, DRD4, DRD5, HRH1, HTR1A, HTR2A, HTR2C, HTR6, HTR7 |
| AMOXAPINE | ChEMBL | Phase 4 (approved) | ADRA2A, ADRA2B, ADRA2C, DRD1, DRD2, DRD3, DRD4, DRD5, HRH1, HTR1A, HTR2A, HTR2C, HTR6, HTR7 |
| ARIPIPRAZOLE | ChEMBL | Phase 4 (approved) | ADRA2A, ADRA2B, ADRA2C, DRD1, DRD2, DRD3, DRD4, DRD5, HRH1, HTR1A, HTR2A, HTR2C, HTR6, HTR7 |
| CARIPRAZINE | ChEMBL | Phase 4 (approved) | ADRA2A, ADRA2B, ADRA2C, DRD1, DRD2, DRD3, DRD4, DRD5, HRH1, HTR1A, HTR2A, HTR2C, HTR6, HTR7 |
| DOXEPIN | ChEMBL | Phase 4 (approved) | ADRA2A, ADRA2B, ADRA2C, DRD1, DRD2, DRD3, DRD4, DRD5, HRH1, HTR1A, HTR2A, HTR2C, HTR6, HTR7 |
| FLUPHENAZINE | ChEMBL | Phase 4 (approved) | ADRA2A, ADRA2B, ADRA2C, DRD1, DRD2, DRD3, DRD4, DRD5, HRH1, HTR1A, HTR2A, HTR2C, HTR6, HTR7 |
| HALOPERIDOL | ChEMBL | Phase 4 (approved) | ADRA2A, ADRA2B, ADRA2C, DRD1, DRD2, DRD3, DRD4, DRD5, HRH1, HTR1A, HTR2A, HTR2C, HTR6, HTR7 |
| LOXAPINE | ChEMBL | Phase 4 (approved) | ADRA2A, ADRA2B, ADRA2C, DRD1, DRD2, DRD3, DRD4, DRD5, HRH1, HTR1A, HTR2A, HTR2C, HTR6, HTR7 |
| PROMAZINE | ChEMBL | Phase 4 (approved) | ADRA2A, ADRA2B, ADRA2C, DRD1, DRD2, DRD3, DRD4, DRD5, HRH1, HTR1A, HTR2A, HTR2C, HTR6, HTR7 |
| RISPERIDONE | ChEMBL | Phase 4 (approved) | ADRA2A, ADRA2B, ADRA2C, DRD1, DRD2, DRD3, DRD4, DRD5, HRH1, HTR1A, HTR2A, HTR2C, HTR6, HTR7 |
| RITANSERIN | ChEMBL | Phase 2 | ADRA2A, ADRA2B, ADRA2C, DRD1, DRD2, DRD3, DRD4, DRD5, HRH1, HTR1A, HTR2A, HTR2C, HTR6, HTR7 |
| TEGASEROD | ChEMBL + PubChem | Phase 4 (approved) | ADRA2A, ADRA2B, ADRA2C, DRD1, DRD2, DRD3, DRD4, DRD5, HTR1A, HTR2A, HTR2C, HTR6, HTR7 |
| AMITRIPTYLINE | ChEMBL | Phase 4 (approved) | ADRA2A, ADRA2B, ADRA2C, DRD1, DRD2, DRD3, DRD4, DRD5, HRH1, HTR1A, HTR2A, HTR2C, HTR6 |
| ASTEMIZOLE | ChEMBL | Phase 4 (approved) | ADRA2A, ADRA2B, ADRA2C, DRD1, DRD2, DRD3, DRD4, HRH1, HTR1A, HTR2A, HTR2C, HTR6, HTR7 |
| IMIPRAMINE | ChEMBL | Phase 4 (approved) | ADRA2B, ADRA2C, DRD1, DRD2, DRD3, DRD4, DRD5, HRH1, HTR1A, HTR2A, HTR2C, HTR6, HTR7 |
| MIANSERIN | ChEMBL | Phase 4 (approved) | ADRA2A, ADRA2B, ADRA2C, DRD1, DRD2, DRD3, DRD4, HRH1, HTR1A, HTR2A, HTR2C, HTR6, HTR7 |
| NEFAZODONE | ChEMBL | Phase 4 (approved) | ADRA2A, ADRA2B, ADRA2C, DRD1, DRD2, DRD3, DRD4, HRH1, HTR1A, HTR2A, HTR2C, HTR6, HTR7 |
| QUETIAPINE | ChEMBL | Phase 4 (approved) | ADRA2A, ADRA2B, ADRA2C, DRD1, DRD2, DRD3, DRD4, HRH1, HTR1A, HTR2A, HTR2C, HTR6, HTR7 |
| THIORIDAZINE | ChEMBL | Phase 4 (approved) | ADRA2A, ADRA2B, ADRA2C, DRD1, DRD2, DRD3, DRD4, HRH1, HTR1A, HTR2A, HTR2C, HTR6, HTR7 |
| THIOTHIXENE | ChEMBL | Phase 4 (approved) | ADRA2A, ADRA2B, ADRA2C, DRD1, DRD2, DRD3, DRD4, HRH1, HTR1A, HTR2A, HTR2C, HTR6, HTR7 |
| ZIPRASIDONE | ChEMBL | Phase 4 (approved) | ADRA2A, ADRA2B, ADRA2C, DRD1, DRD2, DRD3, DRD4, HRH1, HTR1A, HTR2A, HTR2C, HTR6, HTR7 |
| PENFLURIDOL | ChEMBL | Phase 2 | ADRA2B, ADRA2C, DRD1, DRD2, DRD3, DRD4, DRD5, HRH1, HTR1A, HTR2A, HTR2C, HTR6, HTR7 |
| SPIPERONE | ChEMBL | Phase 2 | ADRA2A, ADRA2B, ADRA2C, DRD1, DRD2, DRD3, DRD4, HRH1, HTR1A, HTR2A, HTR2C, HTR6, HTR7 |
| Pyrazinamide | PubChem | Approved | ADRA2A, ADRA2B, ADRA2C, DRD1, DRD2, DRD3, DRD4, HRH1, HTR1A, HTR2A, HTR2C, HTR6, HTR7 |
| DESLORATADINE | ChEMBL + PubChem | Phase 4 (approved) | ADRA2A, ADRA2B, ADRA2C, DRD1, DRD2, DRD3, DRD4, HRH1, HTR1A, HTR2A, HTR2C, HTR6 |
| PALIPERIDONE | ChEMBL + PubChem | Phase 4 (approved) | ADRA2A, ADRA2B, ADRA2C, DRD1, DRD2, DRD3, DRD4, DRD5, HRH1, HTR2A, HTR2C, HTR7 |
| PRAMIPEXOLE | ChEMBL + PubChem | Phase 4 (approved) | ADRA2A, ADRA2B, ADRA2C, DRD1, DRD2, DRD3, DRD4, DRD5, HRH1, HTR1A, HTR2A, HTR7 |
| APOMORPHINE | ChEMBL | Phase 4 (approved) | ADRA2A, ADRA2B, ADRA2C, DRD1, DRD2, DRD3, DRD4, DRD5, HRH1, HTR1A, HTR2A, HTR2C |
| ASENAPINE | ChEMBL | Phase 4 (approved) | ADRA2A, ADRA2B, ADRA2C, DRD1, DRD2, DRD3, DRD4, HRH1, HTR1A, HTR2A, HTR2C, HTR6 |
| CARVEDILOL | ChEMBL | Phase 4 (approved) | ADRA2A, ADRA2B, ADRA2C, DRD1, DRD2, DRD3, DRD4, HTR1A, HTR2A, HTR2C, HTR6, HTR7 |
| CYPROHEPTADINE | ChEMBL | Phase 4 (approved) | ADRA2A, ADRA2B, ADRA2C, DRD1, DRD2, DRD3, HRH1, HTR1A, HTR2A, HTR2C, HTR6, HTR7 |
| EBASTINE | ChEMBL | Phase 4 (approved) | ADRA2A, ADRA2B, ADRA2C, DRD1, DRD2, DRD3, DRD4, HRH1, HTR1A, HTR2A, HTR2C, HTR6 |
| ILOPERIDONE | ChEMBL | Phase 4 (approved) | ADRA2A, ADRA2B, ADRA2C, DRD1, DRD2, DRD3, DRD4, HRH1, HTR1A, HTR2A, HTR2C, HTR6 |
| KETANSERIN | ChEMBL | Phase 4 (approved) | ADRA2B, ADRA2C, DRD1, DRD2, DRD3, DRD4, HRH1, HTR1A, HTR2A, HTR2C, HTR6, HTR7 |
| KETOTIFEN | ChEMBL | Phase 4 (approved) | ADRA2A, ADRA2B, ADRA2C, DRD1, DRD2, DRD3, DRD5, HRH1, HTR2A, HTR2C, HTR6, HTR7 |
| MAPROTILINE | ChEMBL | Phase 4 (approved) | ADRA2A, ADRA2B, ADRA2C, DRD1, DRD2, DRD3, DRD5, HRH1, HTR1A, HTR2A, HTR2C, HTR6 |
| METHYSERGIDE | ChEMBL | Phase 4 (approved) | ADRA2A, ADRA2B, ADRA2C, DRD1, DRD2, DRD3, HRH1, HTR1A, HTR2A, HTR2C, HTR6, HTR7 |
| PERGOLIDE | ChEMBL | Phase 4 (approved) | ADRA2A, ADRA2B, ADRA2C, DRD1, DRD2, DRD3, DRD4, HRH1, HTR1A, HTR2A, HTR2C, HTR6 |
| PIMOZIDE | ChEMBL | Phase 4 (approved) | ADRA2A, ADRA2B, ADRA2C, DRD1, DRD2, DRD3, DRD4, HRH1, HTR1A, HTR2A, HTR2C, HTR6 |
| PROCHLORPERAZINE | ChEMBL | Phase 4 (approved) | ADRA2A, ADRA2B, ADRA2C, DRD1, DRD2, DRD3, DRD4, HRH1, HTR1A, HTR2A, HTR2C, HTR6 |
| PROMETHAZINE | ChEMBL | Phase 4 (approved) | ADRA2A, ADRA2B, ADRA2C, DRD1, DRD2, DRD3, DRD4, HRH1, HTR1A, HTR2A, HTR2C, HTR6 |
| SERTINDOLE | ChEMBL | Phase 4 (approved) | ADRA2A, ADRA2B, ADRA2C, DRD1, DRD2, DRD3, DRD4, HRH1, HTR1A, HTR2A, HTR2C, HTR6 |
| SUNITINIB | ChEMBL | Phase 4 (approved) | ADRA2A, ADRA2B, ADRA2C, DRD1, DRD2, DRD3, DRD4, HRH1, HTR1A, HTR2A, HTR2C, HTR6 |
| LISURIDE | ChEMBL | Phase 3 | ADRA2A, ADRA2B, ADRA2C, DRD1, DRD2, DRD3, DRD4, HRH1, HTR1A, HTR2A, HTR2C, HTR6 |
| FANANSERIN | ChEMBL | Phase 2 | ADRA2A, ADRA2B, ADRA2C, DRD2, DRD3, DRD4, HRH1, HTR1A, HTR2A, HTR2C, HTR6, HTR7 |
| METERGOLINE | ChEMBL | Phase 2 | ADRA2A, ADRA2B, ADRA2C, DRD1, DRD2, DRD3, HRH1, HTR1A, HTR2A, HTR2C, HTR6, HTR7 |
| NIGULDIPINE | ChEMBL | Phase 2 | ADRA2A, ADRA2B, ADRA2C, DRD1, DRD2, DRD3, DRD5, HRH1, HTR1A, HTR2C, HTR6, HTR7 |
| Fidaxomicin | ChEMBL + PubChem | Phase 4 (approved) | ADRA2A, ADRA2B, ADRA2C, DRD1, DRD2, DRD3, DRD4, HRH1, HTR1A, HTR2A, HTR2C |
| Propoxyphene | ChEMBL + PubChem | Phase 4 (approved) | ADRA2A, ADRA2B, ADRA2C, DRD1, DRD2, DRD3, DRD4, HRH1, HTR1A, HTR2A, HTR2C |
| AZELASTINE | ChEMBL | Phase 4 (approved) | ADRA2A, ADRA2B, ADRA2C, DRD1, DRD2, DRD3, HRH1, HTR2A, HTR2C, HTR6, HTR7 |
| BENPERIDOL | ChEMBL | Phase 4 (approved) | ADRA2A, ADRA2B, ADRA2C, DRD1, DRD2, DRD3, DRD4, HRH1, HTR1A, HTR2A, HTR2C |
| BROMOCRIPTINE | ChEMBL | Phase 4 (approved) | ADRA2A, ADRA2B, ADRA2C, DRD1, DRD2, DRD3, DRD4, HTR1A, HTR2A, HTR2C, HTR6 |
| CABERGOLINE | ChEMBL | Phase 4 (approved) | ADRA2A, ADRA2B, ADRA2C, DRD1, DRD2, DRD3, DRD4, DRD5, HRH1, HTR1A, HTR2A |
| CISAPRIDE | ChEMBL | Phase 4 (approved) | ADRA2A, ADRA2B, ADRA2C, DRD1, DRD2, DRD3, HRH1, HTR1A, HTR2A, HTR2C, HTR7 |
| CLEMASTINE | ChEMBL | Phase 4 (approved) | ADRA2A, ADRA2B, ADRA2C, DRD1, DRD2, DRD3, HRH1, HTR1A, HTR2A, HTR2C, HTR6 |
| CLOMIPRAMINE | ChEMBL | Phase 4 (approved) | ADRA2A, ADRA2B, ADRA2C, DRD1, DRD2, DRD3, HRH1, HTR1A, HTR2A, HTR2C, HTR6 |
| CLOTRIMAZOLE | ChEMBL | Phase 4 (approved) | ADRA2A, ADRA2B, ADRA2C, DRD1, DRD2, DRD3, DRD4, HRH1, HTR2A, HTR2C, HTR6 |
Related Atlas pages
- Genes: HTR6, HTR7, HTR1A, DRD1, DRD2, DRD3, DRD4, DRD5, ADRA2A, HRH1, ADRA2B, ADRA2C, TRPC5, HTR2A, HTR2C
- Diseases: psychotic disorder, mental disorder, conduct disorder, porphyria, neonatal abstinence syndrome, severe acute respiratory syndrome
- Drugs: Brexpiprazole, Clozapine, Dihydroergotamine, Olanzapine, Amoxapine, Aripiprazole, Cariprazine, Doxepin, Fluphenazine, Haloperidol, Loxapine, Promazine, Risperidone, Tegaserod, Amitriptyline, Astemizole, Imipramine, Mianserin, Nefazodone, Quetiapine, Thioridazine, Thiothixene, Ziprasidone, Pyrazinamide, Desloratadine, Paliperidone, Pramipexole, Apomorphine, Asenapine, Carvedilol, Cyproheptadine, Ebastine, Iloperidone, Ketanserin, Ketotifen, Maprotiline, Methysergide, Pergolide, Pimozide, Prochlorperazine, Promethazine, Sertindole, Sunitinib, Lisuride, Fidaxomicin, Propoxyphene, Azelastine, Benperidol, Bromocriptine, Cabergoline, Cisapride, Clemastine, Clomipramine, Clotrimazole