Terazosin
drug drugOn this page
Also known as TerazosabbTerazosinaTerazosineTerazocinSID855611SID90340975SID50085853SID174007477C0164458
Summary
Terazosin (CHEMBL611) is an approved small-molecule antineoplastic agent (ATC G04CA03) targeting ADRA1A, ADRA1B, and ADRA1D; indicated across 8 conditions including benign prostatic hyperplasia and hypertensive disorder.
At a glance
- Status: Approved (max clinical phase 4)
- Modality: Small molecule
- ATC class: G04CA03
- Targets: 3 (ADRA1A, ADRA1B, ADRA1D)
- Indications: 8 conditions
- Clinical trials: 16
- Chemistry: 387.4 Da · C19H25N5O4
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL611 |
| Name | Terazosin |
| Type | Small molecule |
| Max phase | 4 |
| FDA approved | yes |
| PubChem CID | 5401 |
| ChEBI | CHEBI:9445 |
| ATC | G04CA03 |
| Molecular formula | C19H25N5O4 |
| Molecular weight | 387.4 |
| InChIKey | VCKUSRYTPJJLNI-UHFFFAOYSA-N |
SMILES: COC1=C(C=C2C(=C1)C(=NC(=N2)N3CCN(CC3)C(=O)C4CCCO4)N)OC
IUPAC name: [4-(4-amino-6,7-dimethoxyquinazolin-2-yl)piperazin-1-yl]-(oxolan-2-yl)methanone
Pharmacological roles (ChEBI): antineoplastic agent, antihypertensive agent, α-adrenergic antagonist.
Also known as: Terazosabb, Terazosin, Terazosina, Terazosine, terazosin, Terazocin, SID855611, SID90340975, SID50085853, TERAZOSINE, SID174007477, TERAZOSIN
Parent form; salt/anhydrous children: CHEMBL1201091, CHEMBL1256665, CHEMBL3989562
Patent coverage: 5,041 distinct patent families (18,696 SureChEMBL compound mentions), from 2 matched compound structure(s). One matched structure accounts for 18,690 (100%) 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 |
|---|---|---|---|---|---|
| ADRA1A | α1A-adrenoceptor | Antagonist | 8.2 | P35348 | |
| ADRA1B | α1B-adrenoceptor | Antagonist | 8.7 | 0% | P35368 |
| ADRA1D | α1D-adrenoceptor | Antagonist | 8.6 | 0.2% | P25100 |
Broader ChEMBL bioactivity targets: 31 (assay-derived). Sample: Lysine-specific demethylase 4E, Survival motor neuron protein, Prelamin-A/C, 15-hydroxyprostaglandin dehydrogenase [NAD(+)], ATP-binding cassette sub-family C member 4, Alpha-2A adrenergic receptor, Adrenergic receptor alpha-1, Alpha-2C adrenergic receptor, Alpha-2B adrenergic receptor, Beta-lactamase, D(1A) dopamine receptor, Adrenergic receptor alpha-1, Acetylcholinesterase, Alpha-1D adrenergic receptor, Alpha-1A adrenergic receptor, Alpha-1B adrenergic receptor, Mu-type opioid receptor, Kappa-type opioid receptor, Voltage-gated inwardly rectifying potassium channel KCNH2, Alpha-galactosidase A.
Bioactivity
ChEMBL activities: 104 potent at pChembl ≥ 5 of 118 total. Top 100 by potency (10 = 0.1 nM, 6 = 1 µM):
| Target | pChembl | Type | Value | Unit | Activity ID |
|---|---|---|---|---|---|
| ADRA1B | 9.3 | EC50 | 0.5 | nM | CHEMBL_ACT_15186194 |
| P18841 | 9.16 | Ki | 0.69 | nM | CHEMBL_ACT_831822 |
| P43140 | 9.09 | Ki | 0.82 | nM | CHEMBL_ACT_831821 |
| ADRA1D | 9.07 | Ki | 0.85 | nM | CHEMBL_ACT_57647 |
| P23944 | 9 | Ki | 1.01 | nM | CHEMBL_ACT_831823 |
| ADRA1B | 8.92 | Ki | 1.2 | nM | CHEMBL_ACT_1000375 |
| ADRA1B | 8.92 | Ki | 1.2 | nM | CHEMBL_ACT_473825 |
| P23944 | 8.83 | Kd | 1.48 | nM | CHEMBL_ACT_15211919 |
| P23944 | 8.83 | Kd | 1.48 | nM | CHEMBL_ACT_18496924 |
| ADRA1B | 8.76 | EC50 | 1.73 | nM | CHEMBL_ACT_16764915 |
| P15823 | 8.72 | Ki | 1.9 | nM | CHEMBL_ACT_1000372 |
| ADRA1B | 8.72 | Ki | 1.9 | nM | CHEMBL_ACT_303826 |
| ADRA1B | 8.72 | Ki | 1.9 | nM | CHEMBL_ACT_677848 |
| ADRA1B | 8.71 | Ki | 1.95 | nM | CHEMBL_ACT_338934 |
| ADRA1D | 8.7 | Ki | 2 | nM | CHEMBL_ACT_1000376 |
| ADRA1D | 8.7 | Ki | 2 | nM | CHEMBL_ACT_473824 |
| ADRA1A | 8.7 | Ki | 2 | nM | CHEMBL_ACT_473830 |
| ADRA1A | 8.7 | Ki | 2 | nM | CHEMBL_ACT_57645 |
| ADRA1B | 8.66 | Ki | 2.2 | nM | CHEMBL_ACT_319204 |
| P15823 | 8.65 | Kd | 2.24 | nM | CHEMBL_ACT_13351504 |
| P23944 | 8.65 | Kd | 2.24 | nM | CHEMBL_ACT_18496951 |
| P23944 | 8.65 | Kd | 2.24 | nM | CHEMBL_ACT_57654 |
| ADRA1A | 8.62 | Ki | 2.4 | nM | CHEMBL_ACT_473828 |
| P18130 | 8.6 | Ki | 2.51 | nM | CHEMBL_ACT_1213818 |
| P15823 | 8.6 | Kd | 2.51 | nM | CHEMBL_ACT_18496950 |
| ADRA1B | 8.6 | Ki | 2.51 | nM | CHEMBL_ACT_274835 |
| P15823 | 8.6 | Kd | 2.51 | nM | CHEMBL_ACT_57653 |
| P15823 | 8.6 | Kd | 2.51 | nM | CHEMBL_ACT_832807 |
| P15823 | 8.59 | Kd | 2.57 | nM | CHEMBL_ACT_15211906 |
| P15823 | 8.59 | Kd | 2.57 | nM | CHEMBL_ACT_18496917 |
| ADRA1B | 8.59 | Ki | 2.6 | nM | CHEMBL_ACT_610323 |
| ADRA1B | 8.57 | Ki | 2.68 | nM | CHEMBL_ACT_57646 |
| ADRA1A | 8.54 | Ki | 2.9 | nM | CHEMBL_ACT_473827 |
| P15823 | 8.48 | Ki | 3.33 | nM | CHEMBL_ACT_7799707 |
| P23944 | 8.47 | Ki | 3.4 | nM | CHEMBL_ACT_1000373 |
| ADRA1D | 8.46 | Ki | 3.5 | nM | CHEMBL_ACT_303827 |
| ADRA1D | 8.46 | Ki | 3.5 | nM | CHEMBL_ACT_319202 |
| ADRA1D | 8.46 | Ki | 3.47 | nM | CHEMBL_ACT_338935 |
| ADRA1D | 8.46 | Ki | 3.5 | nM | CHEMBL_ACT_677849 |
| ADRA1D | 8.43 | Ki | 3.7 | nM | CHEMBL_ACT_610324 |
| P43140 | 8.41 | Ki | 3.9 | nM | CHEMBL_ACT_1000371 |
| ADRA1D | 8.4 | Ki | 3.98 | nM | CHEMBL_ACT_274836 |
| ADRA1A | 8.4 | Ki | 4 | nM | CHEMBL_ACT_303828 |
| ADRA1A | 8.38 | Ki | 4.2 | nM | CHEMBL_ACT_1000374 |
| ADRA1A | 8.38 | Ki | 4.2 | nM | CHEMBL_ACT_473826 |
| ADRA1D | 8.3 | IC50 | 5 | nM | CHEMBL_ACT_24959148 |
| P15823 | 8.22 | IC50 | 6.03 | nM | CHEMBL_ACT_7799706 |
| ADRA1A | 8.16 | Ki | 6.9 | nM | CHEMBL_ACT_303825 |
| ADRA1A | 8.16 | Ki | 6.92 | nM | CHEMBL_ACT_338933 |
| ADRA1A | 8.16 | Ki | 6.9 | nM | CHEMBL_ACT_354747 |
| ADRA1A | 8.16 | Ki | 6.9 | nM | CHEMBL_ACT_610322 |
| ADRA1A | 8.16 | Ki | 6.9 | nM | CHEMBL_ACT_677847 |
| ADRA1A | 8.14 | Ki | 7.3 | nM | CHEMBL_ACT_319206 |
| P19328 | 8.11 | Ki | 7.7 | nM | CHEMBL_ACT_57649 |
| ADRA1D | 8.08 | Ki | 8.36 | nM | CHEMBL_ACT_7799709 |
| P43140 | 8.04 | Kd | 9.12 | nM | CHEMBL_ACT_18496949 |
| P43140 | 8.04 | Kd | 9.12 | nM | CHEMBL_ACT_57652 |
| P43140 | 8.04 | Kd | 9.12 | nM | CHEMBL_ACT_832806 |
| P43140 | 8.02 | Ki | 9.59 | nM | CHEMBL_ACT_7799705 |
| ADRA1A | 7.99 | AC50 | 10.3 | nM | CHEMBL_ACT_25138431 |
| P43140 | 7.9 | Kd | 12.59 | nM | CHEMBL_ACT_15211893 |
| P43140 | 7.9 | Kd | 12.59 | nM | CHEMBL_ACT_18496910 |
| ADRA1D | 7.77 | IC50 | 17 | nM | CHEMBL_ACT_7799708 |
| ADRA1A | 7.73 | AC50 | 18.6 | nM | CHEMBL_ACT_25137948 |
| O02824 | 7.7 | Kd | 19.95 | nM | CHEMBL_ACT_1213820 |
| P43140 | 7.62 | IC50 | 24 | nM | CHEMBL_ACT_7799704 |
| ADRA1D | 7.6 | Kd | 25.12 | nM | CHEMBL_ACT_1213819 |
| P18130 | 7.58 | Ki | 26 | nM | CHEMBL_ACT_319207 |
| ADRA2B | 7.58 | Ki | 26 | nM | CHEMBL_ACT_610326 |
| ADRA1B | 7.52 | Ki | 30 | nM | CHEMBL_ACT_319205 |
| ADRA2B | 7.51 | Ki | 30.9 | nM | CHEMBL_ACT_338937 |
| ADRA1A | 7.5 | Ki | 32 | nM | CHEMBL_ACT_473829 |
| P23944 | 7.46 | Ki | 35 | nM | CHEMBL_ACT_319203 |
| ADRA1A | 7.44 | Kd | 36.31 | nM | CHEMBL_ACT_57651 |
| ADRA1A | 7.44 | Kd | 36.31 | nM | CHEMBL_ACT_832808 |
| ADRA1A | 7.4 | Ki | 39.81 | nM | CHEMBL_ACT_274834 |
| ADRA1D | 7.4 | Kd | 39.81 | nM | CHEMBL_ACT_274840 |
| ADRA1A | 7.29 | EC50 | 51 | nM | CHEMBL_ACT_15186187 |
| ADRA1A | 7.29 | EC50 | 51.89 | nM | CHEMBL_ACT_16764855 |
| ADRA2C | 7.11 | Ki | 78 | nM | CHEMBL_ACT_57650 |
| LMNA | 6.95 | Potency | 112.2 | nM | CHEMBL_ACT_3627800 |
| ADRA2C | 6.77 | Ki | 170 | nM | CHEMBL_ACT_610327 |
| ADRA2B | 6.71 | Ki | 195 | nM | CHEMBL_ACT_7799713 |
| ADRA2C | 6.67 | Ki | 213 | nM | CHEMBL_ACT_319210 |
| ADRA2C | 6.65 | Ki | 223.9 | nM | CHEMBL_ACT_338938 |
| ADRA1A | 6.5 | AC50 | 320 | nM | CHEMBL_ACT_25218093 |
| ADRA2C | 6.46 | AC50 | 350 | nM | CHEMBL_ACT_25147909 |
| ADRA1A | 6.44 | AC50 | 360 | nM | CHEMBL_ACT_25218985 |
| ADRA2B | 6.4 | AC50 | 400 | nM | CHEMBL_ACT_25143734 |
| ADRA2B | 6.38 | Ki | 418 | nM | CHEMBL_ACT_319209 |
| ADRA2B | 6.37 | IC50 | 428 | nM | CHEMBL_ACT_7799712 |
| ADRA2A | 6.26 | Ki | 549.5 | nM | CHEMBL_ACT_338936 |
| ADRA2A | 6.26 | Ki | 550 | nM | CHEMBL_ACT_610325 |
| KDM4E | 6.2 | Potency | 631 | nM | CHEMBL_ACT_3705372 |
| ADRA2C | 6.06 | Ki | 878 | nM | CHEMBL_ACT_7799715 |
| ADRA2A | 5.82 | Ki | 1500 | nM | CHEMBL_ACT_57648 |
| OPRK1 | 5.63 | AC50 | 2363 | nM | CHEMBL_ACT_25129453 |
| OPRM1 | 5.52 | AC50 | 3000 | nM | CHEMBL_ACT_25157470 |
| ADRA2A | 5.43 | Ki | 3702 | nM | CHEMBL_ACT_319208 |
| SMN1 | 5.4 | Potency | 3981 | nM | CHEMBL_ACT_3863881 |
Target pathways
Aggregated over 3 target gene(s): ADRA1A, ADRA1B, ADRA1D.
Top Reactome pathways
9 total, by targets touching each:
| Pathway | Targets | Genes |
|---|---|---|
| Signal Transduction | 3 | ADRA1A, ADRA1B, ADRA1D |
| Signaling by GPCR | 3 | ADRA1A, ADRA1B, ADRA1D |
| Class A/1 (Rhodopsin-like receptors) | 3 | ADRA1A, ADRA1B, ADRA1D |
| Amine ligand-binding receptors | 3 | ADRA1A, ADRA1B, ADRA1D |
| GPCR downstream signalling | 3 | ADRA1A, ADRA1B, ADRA1D |
| Adrenoceptors | 3 | ADRA1A, ADRA1B, ADRA1D |
| G alpha (q) signalling events | 3 | ADRA1A, ADRA1B, ADRA1D |
| G alpha (12/13) signalling events | 3 | ADRA1A, ADRA1B, ADRA1D |
| GPCR ligand binding | 3 | ADRA1A, ADRA1B, ADRA1D |
Dominant GO biological processes
| GO term | Targets |
|---|---|
| signal transduction | 3 |
| G protein-coupled receptor signaling pathway | 3 |
| phospholipase C-activating G protein-coupled receptor signaling pathway | 3 |
| positive regulation of cytosolic calcium ion concentration | 3 |
| cell-cell signaling | 3 |
| positive regulation of MAPK cascade | 3 |
| adenylate cyclase-activating adrenergic receptor signaling pathway | 3 |
| neuron-glial cell signaling | 3 |
| adrenergic receptor signaling pathway | 3 |
| positive regulation of cardiac muscle hypertrophy | 2 |
| intracellular signal transduction | 2 |
| positive regulation of vasoconstriction | 2 |
| regulation of muscle contraction | 2 |
| regulation of vasoconstriction | 2 |
| regulation of cardiac muscle contraction | 2 |
Indications & clinical
Indications
1 approved indication. FDA phase 4, plus an anticancer drug’s labelled cancer uses (which ChEMBL often logs at phase 3).
| Indication | Phase | MONDO | EFO |
|---|---|---|---|
| benign prostatic hyperplasia | 4 | MONDO:0010811 | EFO:0000284 |
6 diseases in clinical trials (phase 1–3, investigational — not approved indications). Highest ChEMBL trial phase per disease; a non-cancer approved use is occasionally logged at phase 3 here.
| Disease (in trials) | Phase | MONDO | EFO |
|---|---|---|---|
| hypertensive disorder | 3 | MONDO:0005044 | EFO:0000537 |
| atherosclerosis | 3 | MONDO:0005311 | EFO:0003914 |
| coronary artery disorder | 3 | MONDO:0005010 | EFO:0001645 |
| type 2 diabetes mellitus | 3 | MONDO:0005148 | MONDO:0005148 |
| internal carotid artery stenosis | 2 | MONDO:0005189 | EFO:0002615 |
| Parkinson disease | 1 | MONDO:0005180 | MONDO:0005180 |
1 further indication record had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.
Clinical trials
Total trials: 16.
Phase distribution
| Phase | Trials |
|---|---|
| PHASE2 | 4 |
| Not specified | 4 |
| PHASE4 | 2 |
| PHASE3 | 2 |
| PHASE2/PHASE3 | 1 |
| PHASE1/PHASE2 | 1 |
| PHASE1 | 1 |
| EARLY_PHASE1 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT05855577 | PHASE4 | NOT_YET_RECRUITING | Motor Function Efficacy of Pharmacological Treatments Targeting Energy Metabolism, in Parkinson’s Patients |
| NCT00449683 | PHASE4 | COMPLETED | Excessive Sweating Caused by Antidepressants: Measurement and Treatment With Terazosin |
| NCT06966804 | PHASE3 | RECRUITING | Comparison of Alpha Blockers (Terazosin and Tamsulosin) in Reducing Ureteral Stent Related Symptoms |
| NCT07207057 | PHASE3 | RECRUITING | Edmond J. Safra Accelerating Clinical Trials in Parkinson’s Disease: A Multiarm Multi-stage Platform Trial |
| NCT01530243 | PHASE2/PHASE3 | COMPLETED | The Effect of Terazosin and Tolterodine on Ureteral Stent Related Symptoms |
| NCT04386317 | PHASE2 | ACTIVE_NOT_RECRUITING | Terazosin Effect on Cardiac Changes in Early Parkinson’s Disease |
| NCT05109364 | PHASE2 | ACTIVE_NOT_RECRUITING | Terazosin and Parkinson’s Disease Extension Study |
| NCT07464028 | PHASE2 | NOT_YET_RECRUITING | Terazosin And Metabolic Energetics in Parkinson’s Disease |
| NCT03195673 | PHASE2 | UNKNOWN | Safety and Efficacy of Low Dosage of Terazosin in Subjects Undergoing Carotid Artery Stenting |
| NCT03905811 | PHASE1/PHASE2 | COMPLETED | A Pilot Study of Terazosin for Parkinson’s Disease |
| NCT04551040 | PHASE1 | ACTIVE_NOT_RECRUITING | Target Engagement of Terazosin in Healthy Adults |
| NCT07224269 | EARLY_PHASE1 | NOT_YET_RECRUITING | Effect of Terazosin on ATP Levels in People With Amyotrophic Lateral Sclerosis |
| NCT00237510 | Not specified | COMPLETED | Pilot Study of Terazosin in Treatment of Antidepressant Induced Excessive Sweating |
| NCT00563485 | Not specified | TERMINATED | Randomized Trial Comparing Terazosin 5 mg Daily and Doxazosin GITS 4 mg Daily for Trial Without Catheter in Acute Urinary Retention With Long Term Follow up |
| NCT00693199 | Not specified | COMPLETED | Effect of Amlodipine Monotherapy or Combined With Terazosin on Lower Urinary Tract Symptoms and Hypertension |
| NCT01508637 | Not specified | UNKNOWN | Diesel Exhaust and Vascular Function |
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.
571 molecules share ≥1 primary target. Top 100 by shared-target count:
| Molecule | Source | Status | Shared targets |
|---|---|---|---|
| DIHYDROERGOTAMINE | ChEMBL + PubChem | Phase 4 (approved) | ADRA1A, ADRA1B, ADRA1D |
| ALFUZOSIN | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1B, ADRA1D |
| AMLODIPINE | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1B, ADRA1D |
| APRACLONIDINE | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1B, ADRA1D |
| ARIPIPRAZOLE | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1B, ADRA1D |
| ASENAPINE | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1B, ADRA1D |
| ATENOLOL | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1B, ADRA1D |
| AZELASTINE | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1B, ADRA1D |
| BREXPIPRAZOLE | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1B, ADRA1D |
| BRIMONIDINE | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1B, ADRA1D |
| BUSPIRONE | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1B, ADRA1D |
| CARIPRAZINE | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1B, ADRA1D |
| CISAPRIDE | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1B, ADRA1D |
| CLONIDINE | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1B, ADRA1D |
| CLOZAPINE | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1B, ADRA1D |
| DEXMEDETOMIDINE | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1B, ADRA1D |
| DOPAMINE | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1B, ADRA1D |
| DOXAZOSIN | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1B, ADRA1D |
| EBASTINE | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1B, ADRA1D |
| EPINEPHRINE | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1B, ADRA1D |
| FENOLDOPAM | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1B, ADRA1D |
| HALOPERIDOL | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1B, ADRA1D |
| INDACATEROL | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1B, ADRA1D |
| INDORAMIN | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1B, ADRA1D |
| ISOPROTERENOL | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1B, ADRA1D |
| LABETALOL | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1B, ADRA1D |
| MOXISYLYTE | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1B, ADRA1D |
| NAFTOPIDIL | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1B, ADRA1D |
| NEFAZODONE | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1B, ADRA1D |
| NOREPINEPHRINE | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1B, ADRA1D |
| OLANZAPINE | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1B, ADRA1D |
| OXYMETAZOLINE | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1B, ADRA1D |
| PHENTOLAMINE | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1B, ADRA1D |
| PRAZOSIN | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1B, ADRA1D |
| QUETIAPINE | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1B, ADRA1D |
| RISPERIDONE | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1B, ADRA1D |
| SERTINDOLE | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1B, ADRA1D |
| SILODOSIN | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1B, ADRA1D |
| TAMSULOSIN | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1B, ADRA1D |
| TEGASEROD | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1B, ADRA1D |
| TERFENADINE | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1B, ADRA1D |
| TOLAZOLINE | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1B, ADRA1D |
| VERAPAMIL | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1B, ADRA1D |
| VILAZODONE | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1B, ADRA1D |
| XYLOMETAZOLINE | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1B, ADRA1D |
| ZIPRASIDONE | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1B, ADRA1D |
| BUNAZOSIN | ChEMBL | Phase 3 | ADRA1A, ADRA1B, ADRA1D |
| IDAZOXAN | ChEMBL | Phase 3 | ADRA1A, ADRA1B, ADRA1D |
| LATREPIRDINE | ChEMBL | Phase 3 | ADRA1A, ADRA1B, ADRA1D |
| MEDETOMIDINE | ChEMBL | Phase 3 | ADRA1A, ADRA1B, ADRA1D |
| YOHIMBINE | ChEMBL | Phase 3 | ADRA1A, ADRA1B, ADRA1D |
| ABANOQUIL | ChEMBL | Phase 2 | ADRA1A, ADRA1B, ADRA1D |
| CIRAZOLINE | ChEMBL | Phase 2 | ADRA1A, ADRA1B, ADRA1D |
| DEXNIGULDIPINE | ChEMBL | Phase 2 | ADRA1A, ADRA1B, ADRA1D |
| IPSAPIRONE | ChEMBL | Phase 2 | ADRA1A, ADRA1B, ADRA1D |
| MAZAPERTINE | ChEMBL | Phase 2 | ADRA1A, ADRA1B, ADRA1D |
| NIGULDIPINE | ChEMBL | Phase 2 | ADRA1A, ADRA1B, ADRA1D |
| PIPEROXAN | ChEMBL | Phase 2 | ADRA1A, ADRA1B, ADRA1D |
| PIZOTYLINE | ChEMBL | Phase 2 | ADRA1A, ADRA1B, ADRA1D |
| SPIRAMIDE | ChEMBL | Phase 2 | ADRA1A, ADRA1B, ADRA1D |
| SPIROXATRINE | ChEMBL | Phase 2 | ADRA1A, ADRA1B, ADRA1D |
| TASIPIMIDINE | ChEMBL | Phase 2 | ADRA1A, ADRA1B, ADRA1D |
| UPIDOSIN | ChEMBL | Phase 2 | ADRA1A, ADRA1B, ADRA1D |
| ZOTEPINE | ChEMBL | Phase 2 | ADRA1A, ADRA1B, ADRA1D |
| GENTIAN VIOLET | ChEMBL + PubChem | Phase 4 (approved) | ADRA1A, ADRA1D |
| PRAMIPEXOLE | ChEMBL + PubChem | Phase 4 (approved) | ADRA1A, ADRA1D |
| AMITRIPTYLINE | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1D |
| AMOXAPINE | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1D |
| APOMORPHINE | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1D |
| ASTEMIZOLE | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1D |
| BENZTROPINE | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1D |
| BROMOCRIPTINE | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1D |
| CARVEDILOL | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1D |
| CHLORPROMAZINE | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1D |
| CINNARIZINE | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1D |
| CITALOPRAM | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1D |
| CLEMASTINE | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1D |
| CLOMIPRAMINE | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1D |
| CYPROHEPTADINE | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1D |
| DAPIPRAZOLE | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1D |
| DIETHYLSTILBESTROL | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1D |
| DOBUTAMINE | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1D |
| DOMPERIDONE | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1D |
| DOXEPIN | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1D |
| ERGOTAMINE | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1D |
| FENTANYL | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1B |
| FLUPHENAZINE | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1D |
| GUANABENZ | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1D |
| GUANFACINE | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1D |
| IMIQUIMOD | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1D |
| KETOTIFEN | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1D |
| LOPERAMIDE | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1B |
| LUMATEPERONE TOSYLATE | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1B |
| MAPROTILINE | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1D |
| MEPAZINE | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1D |
| MIANSERIN | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1D |
| NORTRIPTYLINE | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1D |
| PERGOLIDE | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1D |
| PHENYLEPHRINE | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1B |
| PROCHLORPERAZINE | ChEMBL | Phase 4 (approved) | ADRA1A, ADRA1D |
Related Atlas pages
- Genes: ADRA1A, ADRA1B, ADRA1D
- Indicated for: benign prostatic hyperplasia
- In clinical trials for: hypertensive disorder, atherosclerosis, coronary artery disorder, type 2 diabetes mellitus, internal carotid artery stenosis
- Drugs: Dihydroergotamine, Alfuzosin, Amlodipine, Apraclonidine, Aripiprazole, Asenapine, Atenolol, Azelastine, Brexpiprazole, Brimonidine, Buspirone, Cariprazine, Cisapride, Clonidine, Clozapine, Dexmedetomidine, Dopamine, Doxazosin, Ebastine, Epinephrine, Fenoldopam, Haloperidol, Indacaterol, Indoramin, Isoproterenol, Labetalol, Moxisylyte, Naftopidil, Nefazodone, Norepinephrine, Olanzapine, Oxymetazoline, Phentolamine, Prazosin, Quetiapine, Risperidone, Sertindole, Silodosin, Tamsulosin, Tegaserod, Terfenadine, Tolazoline, Verapamil, Vilazodone, Xylometazoline, Ziprasidone, Bunazosin, Idazoxan, Latrepirdine, Yohimbine, Pramipexole, Amitriptyline, Amoxapine, Apomorphine, Astemizole, Benztropine, Bromocriptine, Carvedilol, Chlorpromazine, Cinnarizine, Citalopram, Clemastine, Clomipramine, Cyproheptadine, Dapiprazole, Diethylstilbestrol, Dobutamine, Domperidone, Doxepin, Ergotamine, Fentanyl, Fluphenazine, Guanabenz, Guanfacine, Imiquimod, Ketotifen, Loperamide, Lumateperone Tosylate, Maprotiline, Mepazine, Mianserin, Nortriptyline, Pergolide, Phenylephrine, Prochlorperazine