Lesinurad
Urate Transporter 1 Inhibitor — MUSCULO-SKELETAL SYSTEM
Also known as: RDEA594, RDEA594 Sodium, zurampic
Data last refreshed: (DrugCentral release 2024-11-01)
Key facts
Lesinurad is an ofm drug in the Urate Transporter 1 Inhibitor class catalogued in DrugCentral. It was first approved by the FDA in 2015. Its mechanism of action is classified as Cytochrome P450 3A Inducers and Urate Transporter 1 Inhibitors. DrugCentral lists 2 molecular targets, including SLC22A11 and SLC22A12. Recorded indications include Hyperuricemia.
- Approval status: ofm (first approved 2015 by the FDA).
- Drug class: Urate Transporter 1 Inhibitor.
- Mechanism of action: Cytochrome P450 3A Inducers; Urate Transporter 1 Inhibitors.
- Molecular targets: SLC22A11 and SLC22A12 (2 listed in DrugCentral).
- Indications: Hyperuricemia.
- ATC code: M04AB05 (Preparations increasing uric acid excretion).
- Molecular formula: C17H14BrN3O2S; molecular weight 404.28 g/mol.
Indications & contraindications
Drug–disease relationships curated by DrugCentral (OMOP / SNOMED concepts).
Indications (1)
- Hyperuricemia
Mechanism & targets
| Mechanism of action (MoA) | Cytochrome P450 3A Inducers; Urate Transporter 1 Inhibitors |
|---|---|
| Established pharmacologic class | Urate Transporter 1 Inhibitor |
Molecular targets (2)
| Target | Gene | Action | Activity |
|---|---|---|---|
| Solute carrier family 22 member 11 | SLC22A11 | inhibitor | IC50 5.43 |
| Solute carrier family 22 member 12 | SLC22A12 | inhibitor | IC50 5.14 |
Regulatory approvals (2)
| Date | Agency | Marketed as | Applicant | Orphan |
|---|---|---|---|---|
| 2016-02-18 | EMA | — | AstraZeneca AB | |
| 2015-12-22 | FDA | — | ARDEA BIOSCIENCES INC |
ATC classification
| ATC code | Therapeutic hierarchy |
|---|---|
M04AB05 | MUSCULO-SKELETAL SYSTEM › ANTIGOUT PREPARATIONS › ANTIGOUT PREPARATIONS › Preparations increasing uric acid excretion |
Pharmacogenomics
Drug-label and guideline annotations from PharmGKB and CPIC.
- EMA label: CYP2C9 · Actionable PGx
- FDA label: CYP2C9 · Actionable PGx
- Swissmedic label: CYP2C9 · Informative PGx
Chemical structure
Full physicochemical, ADMET and 3D-structure analysis of Lesinurad is on its molecule page.
| Molecular formula | C17H14BrN3O2S |
|---|---|
| Molecular weight | 404.28 g/mol |
| CAS number | 878672-00-5 |
| InChIKey | FGQFOYHRJSUHMR-UHFFFAOYSA-N |
| PubChem CID | 53465279 |
Frequently asked questions
Answers are generated from the structured data on this page, not written by hand.
What is Lesinurad used for?
DrugCentral lists the following indications for Lesinurad: Hyperuricemia.
How does Lesinurad work?
Lesinurad is classified as Cytochrome P450 3A Inducers and Urate Transporter 1 Inhibitors; its molecular targets in DrugCentral include SLC22A11 (inhibitor) and SLC22A12 (inhibitor).
When was Lesinurad first approved?
Lesinurad was first approved by the FDA in 2015.
What drug class does Lesinurad belong to?
Lesinurad is in the Urate Transporter 1 Inhibitor class.
What is the chemical formula of Lesinurad?
Lesinurad has the molecular formula C17H14BrN3O2S and a molecular weight of 404.28 g/mol.
Browse: all drugs starting with L · drug guides by category · protein targets A–Z.
Sources
- DrugCentral drug card 5075 — structure, indications, targets, approvals, pharmacologic classes (CC BY-SA 4.0)
- ChEMBL CHEMBL2105716 — compound record and bioactivity
- PubChem CID 53465279 — chemical identifiers
- DrugBank DB11560 — drug record
- FDA UNII 09ERP08I3W — substance identity
- DailyMed: FDA labels for Lesinurad — current prescribing information (label search)
- UniProt Q9NSA0 (SLC22A11) — target protein
- UniProt Q96S37 (SLC22A12) — target protein
- PharmGKB / CPIC — pharmacogenomic label annotations
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