Prazosin
alpha-Adrenergic Blocker — CARDIOVASCULAR SYSTEM
Also known as: furazosin, prazosin HCl, prazosin hydrochloride
Data last refreshed: (DrugCentral release 2024-11-01)
Key facts
Prazosin is an ofp drug in the alpha-Adrenergic Blocker class catalogued in DrugCentral. It was first approved by the FDA in 1976. Its mechanism of action is classified as Adrenergic alpha-Antagonists. DrugCentral lists 40 molecular targets, including Adra1b|Adra1d|Adra1a, ADRA1A and Adra1a. Recorded indications include Hypertensive disorder.
- Approval status: ofp (first approved 1976 by the FDA).
- Drug class: alpha-Adrenergic Blocker.
- Mechanism of action: Adrenergic alpha-Antagonists.
- Molecular targets: Adra1b|Adra1d|Adra1a, ADRA1A, Adra1a and Adra1b (40 listed in DrugCentral).
- Indications: Hypertensive disorder.
- ATC code: C02CA01 (Alpha-adrenoreceptor antagonists).
- Molecular formula: C19H21N5O4; molecular weight 383.41 g/mol.
Indications & contraindications
Drug–disease relationships curated by DrugCentral (OMOP / SNOMED concepts).
Indications (1)
- Hypertensive disorder
Off-label uses (3)
- Benign prostatic hyperplasia
- Chronic Post Traumatic Stress Disorder with Trauma-related Nightmares
- PTSD related nightmares
Contraindications (6)
- Cataract surgery
- End stage renal disease
- Intraoperative floppy iris syndrome
- Micturition syncope
- Narcolepsy
- Syncope
Mechanism & targets
| Mechanism of action (MoA) | Adrenergic alpha-Antagonists |
|---|---|
| Established pharmacologic class | alpha-Adrenergic Blocker |
Molecular targets (40)
| Target | Gene | Action | Activity |
|---|---|---|---|
| Adrenergic receptor alpha-1 | Adra1b|Adra1d|Adra1a | unknown | Kd 10.99 |
| Alpha-1A adrenergic receptor | ADRA1A | inverse agonist | Ki 10.40 |
| Alpha-1A adrenergic receptor | Adra1a | unknown | Ki 10.15 |
| Alpha-1B adrenergic receptor | Adra1b | unknown | Ki 10.00 |
| Alpha-1A adrenergic receptor | ADRA1A | unknown | Ki 9.77 |
| Alpha-1D adrenergic receptor | Adra1d | unknown | Ki 9.70 |
| Alpha-1D adrenergic receptor | ADRA1D | inverse agonist | Ki 9.70 |
| Mu-type opioid receptor | Oprm1 | unknown | Ki 9.70 |
| Alpha-1B adrenergic receptor | ADRA1B | inverse agonist | Ki 9.68 |
| 5-hydroxytryptamine receptor 1D | HTR1D | unknown | Ki 9.48 |
| Beta-casein | Csn2 | unknown | Ki 9.44 |
| Adrenergic receptor alpha-2 | Adra2b|Adra2c|Adra2a | unknown | Ki 9.40 |
| Alpha-1B adrenergic receptor | ADRA1B | unknown | Ki 9.08 |
| Adenosine receptor A3 | ADORA3 | unknown | IC50 9.07 |
| Ribosyldihydronicotinamide dehydrogenase [quinone] | NQO2 | unknown | IC50 8.11 |
| Alpha-2 adrenergic receptor | Adra2b|Adra2c|Adra2a | unknown | Ki 7.89 |
| Alpha-2B adrenergic receptor | ADRA2B | unknown | Ki 7.89 |
| 5-hydroxytryptamine receptor 2A | HTR2A | unknown | Ki 7.73 |
| Alpha-2C adrenergic receptor | ADRA2C | unknown | Ki 7.62 |
| Alpha-2A adrenergic receptor | ADRA2A | unknown | Ki 6.97 |
Regulatory approvals (1)
| Date | Agency | Marketed as | Applicant | Orphan |
|---|---|---|---|---|
| 1976-06-23 | FDA | — | PFIZER |
ATC classification
| ATC code | Therapeutic hierarchy |
|---|---|
C02CA01 | CARDIOVASCULAR SYSTEM › ANTIHYPERTENSIVES › ANTIADRENERGIC AGENTS, PERIPHERALLY ACTING › Alpha-adrenoreceptor antagonists |
C02LE01 | CARDIOVASCULAR SYSTEM › ANTIHYPERTENSIVES › ANTIHYPERTENSIVES AND DIURETICS IN COMBINATION › Alpha-adrenoreceptor antagonists and diuretics |
Reported adverse-event signals
Strongest FDA FAERS disproportionality signals (log-likelihood ratio). A signal is a statistical association in spontaneous reports, not proof that the drug causes the event.
| MedDRA term | LLR |
|---|---|
| Completed suicide | 232.6 |
| Body mass index abnormal | 136.4 |
| Analgesic drug level above therapeutic | 131.6 |
| Suicidal ideation | 126.8 |
| Central nervous system lupus | 122.3 |
| Antidepressant drug level above therapeutic | 118.3 |
| Post-traumatic stress disorder | 118.3 |
| Serositis | 117.3 |
| Priapism | 97.8 |
| Dissociation | 94.4 |
| Atrioventricular block first degree | 86.3 |
| Lupus nephritis | 86.2 |
Chemical structure
Full physicochemical, ADMET and 3D-structure analysis of Prazosin is on its molecule page.
| Molecular formula | C19H21N5O4 |
|---|---|
| Molecular weight | 383.41 g/mol |
| CAS number | 19216-56-9 |
| InChIKey | IENZQIKPVFGBNW-UHFFFAOYSA-N |
| PubChem CID | 4893 |
Frequently asked questions
Answers are generated from the structured data on this page, not written by hand.
What is Prazosin used for?
DrugCentral lists the following indications for Prazosin: Hypertensive disorder.
How does Prazosin work?
Prazosin is classified as Adrenergic alpha-Antagonists; its molecular targets in DrugCentral include Adra1b|Adra1d|Adra1a, ADRA1A (inverse agonist), Adra1a and Adra1b.
When was Prazosin first approved?
Prazosin was first approved by the FDA in 1976.
What drug class does Prazosin belong to?
Prazosin is in the alpha-Adrenergic Blocker class.
What is the chemical formula of Prazosin?
Prazosin has the molecular formula C19H21N5O4 and a molecular weight of 383.41 g/mol.
Browse: all drugs starting with P · drug guides by category · protein targets A–Z.
Sources
- DrugCentral drug card 4209 — structure, indications, targets, approvals, pharmacologic classes (CC BY-SA 4.0)
- ChEMBL CHEMBL1558 — compound record and bioactivity
- PubChem CID 4893 — chemical identifiers
- DrugBank DB00457 — drug record
- FDA UNII XM03YJ541D — substance identity
- DailyMed: FDA labels for Prazosin — current prescribing information (label search)
- UniProt P35348 (ADRA1A) — target protein
- UniProt P25100 (ADRA1D) — target protein
- UniProt P35368 (ADRA1B) — target protein
- UniProt P28221 (HTR1D) — target protein
- UniProt P0DMS8 (ADORA3) — target protein
- UniProt P16083 (NQO2) — target protein
- FDA Adverse Event Reporting System (openFDA FAERS) — adverse-event signals, as aggregated by DrugCentral
How this page is built: methodology · editorial policy & corrections.
For research and educational use only — not medical advice. This page is compiled automatically from public databases. It is not written or reviewed by a clinician. Do not start, stop or change any treatment based on it; consult a qualified healthcare professional. Spotted an error? See our corrections policy or email hello@molforge.ai.