Urapidil
CARDIOVASCULAR SYSTEM
Also known as: ebrantil, eupressyl, mediatensyl, urapidil HCl, urapidil hydrochloride, uraprene, uropidil
Data last refreshed: (DrugCentral release 2024-11-01)
Key facts
Urapidil is a drug catalogued in DrugCentral. It was first approved by the YEAR INTRODUCED in 1981. DrugCentral lists 4 molecular targets, including HTR1A, ADRA1A and ADRA1D. Recorded indications include Hypertensive emergency.
- Molecular targets: HTR1A, ADRA1A, ADRA1D and ADRA1B (4 listed in DrugCentral).
- Indications: Hypertensive emergency.
- ATC code: C02CA06 (Alpha-adrenoreceptor antagonists).
- Molecular formula: C20H29N5O3; molecular weight 387.48 g/mol.
Indications & contraindications
Drug–disease relationships curated by DrugCentral (OMOP / SNOMED concepts).
Indications (1)
- Hypertensive emergency
Mechanism & targets
Molecular targets (4)
| Target | Gene | Action | Activity |
|---|---|---|---|
| 5-hydroxytryptamine receptor 1A | HTR1A | unknown | Ki 9.46 |
| Alpha-1A adrenergic receptor | ADRA1A | antagonist | Ki 8.85 |
| Alpha-1D adrenergic receptor | ADRA1D | antagonist | Ki 7.90 |
| Alpha-1B adrenergic receptor | ADRA1B | antagonist | Ki 7.10 |
Regulatory approvals (1)
| Date | Agency | Marketed as | Applicant | Orphan |
|---|---|---|---|---|
| 1981-01-01 | YEAR INTRODUCED | — | — |
ATC classification
| ATC code | Therapeutic hierarchy |
|---|---|
C02CA06 | CARDIOVASCULAR SYSTEM › ANTIHYPERTENSIVES › ANTIADRENERGIC AGENTS, PERIPHERALLY ACTING › Alpha-adrenoreceptor antagonists |
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 |
|---|---|
| Acute kidney injury | 551.3 |
| Hyperkalaemia | 280.1 |
| Hyponatraemia | 207.3 |
| Rash maculo-papular | 160.1 |
| Eosinophilia | 138.6 |
| Hepatic cytolysis | 134.6 |
| Toxic epidermal necrolysis | 130.3 |
| Bradycardia | 120.9 |
| Product prescribing error | 111.0 |
| Hypotension | 108.6 |
| Fall | 105.4 |
| Hypoglycaemia | 102.4 |
Chemical structure
Full physicochemical, ADMET and 3D-structure analysis of Urapidil is on its molecule page.
| Molecular formula | C20H29N5O3 |
|---|---|
| Molecular weight | 387.48 g/mol |
| CAS number | 34661-75-1 |
| InChIKey | ICMGLRUYEQNHPF-UHFFFAOYSA-N |
| PubChem CID | 5639 |
Frequently asked questions
Answers are generated from the structured data on this page, not written by hand.
What is Urapidil used for?
DrugCentral lists the following indications for Urapidil: Hypertensive emergency.
How does Urapidil work?
Its molecular targets in DrugCentral include HTR1A, ADRA1A (antagonist), ADRA1D (antagonist) and ADRA1B (antagonist).
When was Urapidil first approved?
Urapidil was first approved by the YEAR INTRODUCED in 1981.
What is the chemical formula of Urapidil?
Urapidil has the molecular formula C20H29N5O3 and a molecular weight of 387.48 g/mol.
Browse: all drugs starting with U · drug guides by category · protein targets A–Z.
Sources
- DrugCentral drug card 2796 — structure, indications, targets, approvals, pharmacologic classes (CC BY-SA 4.0)
- ChEMBL CHEMBL1256716 — compound record and bioactivity
- PubChem CID 5639 — chemical identifiers
- DrugBank DB12661 — drug record
- FDA UNII A78GF17HJS — substance identity
- UniProt P08908 (HTR1A) — target protein
- UniProt P35348 (ADRA1A) — target protein
- UniProt P25100 (ADRA1D) — target protein
- UniProt P35368 (ADRA1B) — 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.