Silodosin
alpha-Adrenergic Blocker — GENITO URINARY SYSTEM AND SEX HORMONES
Also known as: rapaflo, silodoshin, silodyx, urief, urorec
Data last refreshed: (DrugCentral release 2024-11-01)
Key facts
Silodosin is an ofp drug in the alpha-Adrenergic Blocker class catalogued in DrugCentral. It was first approved by the FDA in 2008. Its mechanism of action is classified as Adrenergic alpha-Antagonists. DrugCentral lists 19 molecular targets, including ADRA1A, Adra1a and ADRA1D. Recorded indications include Benign prostatic hyperplasia.
- Approval status: ofp (first approved 2008 by the FDA).
- Drug class: alpha-Adrenergic Blocker.
- Mechanism of action: Adrenergic alpha-Antagonists.
- Molecular targets: ADRA1A, Adra1a, ADRA1D and ADRA1B (19 listed in DrugCentral).
- Indications: Benign prostatic hyperplasia.
- ATC code: G04CA04 (Alpha-adrenoreceptor antagonists).
- Molecular formula: C25H32F3N3O4; molecular weight 495.54 g/mol.
Indications & contraindications
Drug–disease relationships curated by DrugCentral (OMOP / SNOMED concepts).
Indications (1)
- Benign prostatic hyperplasia
Contraindications (6)
- Acute nephropathy
- Cataract surgery
- Hepatic failure
- Intraoperative floppy iris syndrome
- Kidney disease
- Orthostatic hypotension
Mechanism & targets
| Mechanism of action (MoA) | Adrenergic alpha-Antagonists |
|---|---|
| Established pharmacologic class | alpha-Adrenergic Blocker |
Molecular targets (19)
| Target | Gene | Action | Activity |
|---|---|---|---|
| Alpha-1A adrenergic receptor | ADRA1A | antagonist | Ki 10.44 |
| Alpha-1A adrenergic receptor | Adra1a | unknown | IC50 9.10 |
| Alpha-1D adrenergic receptor | ADRA1D | antagonist | Ki 8.70 |
| Alpha-1B adrenergic receptor | ADRA1B | antagonist | Ki 7.70 |
| Beta-2 adrenergic receptor | ADRB2 | unknown | Ki 7.48 |
| 5-hydroxytryptamine receptor 1A | HTR1A | unknown | Ki 7.33 |
| D(3) dopamine receptor | DRD3 | unknown | Ki 7.14 |
| 5-hydroxytryptamine receptor 1D | HTR1D | unknown | Ki 7.04 |
| Alpha-2C adrenergic receptor | ADRA2C | unknown | Ki 6.44 |
| 5-hydroxytryptamine receptor 1B | HTR1B | unknown | Ki 6.43 |
| 5-hydroxytryptamine receptor 7 | HTR7 | unknown | Ki 6.32 |
| Alpha-2A adrenergic receptor | ADRA2A | unknown | Ki 6.17 |
| Alpha-2B adrenergic receptor | ADRA2B | unknown | Ki 6.11 |
| D(2) dopamine receptor | DRD2 | unknown | Ki 6.00 |
| D(4) dopamine receptor | DRD4 | unknown | Ki 5.80 |
| 5-hydroxytryptamine receptor 2B | HTR2B | unknown | Ki 5.68 |
| Histamine H1 receptor | HRH1 | unknown | Ki 5.45 |
| Potassium voltage-gated channel subfamily H member 2 | KCNH2 | unknown | IC50 5.09 |
| Multidrug resistance protein 1 | ABCB1 | unknown | — |
Regulatory approvals (2)
| Date | Agency | Marketed as | Applicant | Orphan |
|---|---|---|---|---|
| 2010-01-29 | EMA | — | — | |
| 2008-10-08 | FDA | — | ACTAVIS LABS UT INC |
ATC classification
| ATC code | Therapeutic hierarchy |
|---|---|
G04CA04 | GENITO URINARY SYSTEM AND SEX HORMONES › UROLOGICALS › DRUGS USED IN BENIGN PROSTATIC HYPERTROPHY › 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 |
|---|---|
| Urinary retention | 243.6 |
| Reversible airways obstruction | 140.9 |
| Acute kidney injury | 134.5 |
| Interstitial lung disease | 130.0 |
| Hyponatraemia | 90.9 |
| Erectile dysfunction | 89.2 |
| Cerebral infarction | 79.6 |
| Retrograde ejaculation | 72.3 |
| Inappropriate antidiuretic hormone secretion | 68.9 |
| Haematuria | 68.4 |
| Granulomatous rosacea | 67.1 |
| Orthostatic hypotension | 64.2 |
Chemical structure
Full physicochemical, ADMET and 3D-structure analysis of Silodosin is on its molecule page.
| Molecular formula | C25H32F3N3O4 |
|---|---|
| Molecular weight | 495.54 g/mol |
| CAS number | 160970-54-7 |
| InChIKey | PNCPYILNMDWPEY-QGZVFWFLSA-N |
| PubChem CID | 5312125 |
Frequently asked questions
Answers are generated from the structured data on this page, not written by hand.
What is Silodosin used for?
DrugCentral lists the following indications for Silodosin: Benign prostatic hyperplasia.
How does Silodosin work?
Silodosin is classified as Adrenergic alpha-Antagonists; its molecular targets in DrugCentral include ADRA1A (antagonist), Adra1a, ADRA1D (antagonist) and ADRA1B (antagonist).
When was Silodosin first approved?
Silodosin was first approved by the FDA in 2008.
What drug class does Silodosin belong to?
Silodosin is in the alpha-Adrenergic Blocker class.
What is the chemical formula of Silodosin?
Silodosin has the molecular formula C25H32F3N3O4 and a molecular weight of 495.54 g/mol.
Browse: all drugs starting with S · drug guides by category · protein targets A–Z.
Sources
- DrugCentral drug card 4151 — structure, indications, targets, approvals, pharmacologic classes (CC BY-SA 4.0)
- ChEMBL CHEMBL24778 — compound record and bioactivity
- PubChem CID 5312125 — chemical identifiers
- DrugBank DB06207 — drug record
- FDA UNII CUZ39LUY82 — substance identity
- DailyMed: FDA labels for Silodosin — current prescribing information (label search)
- UniProt P35348 (ADRA1A) — target protein
- UniProt P25100 (ADRA1D) — target protein
- UniProt P35368 (ADRA1B) — target protein
- UniProt P07550 (ADRB2) — target protein
- UniProt P08908 (HTR1A) — target protein
- UniProt P35462 (DRD3) — target protein
- FDA Adverse Event Reporting System (openFDA FAERS) — adverse-event signals, as aggregated by DrugCentral
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