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Chemistry

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Also known as: 878672-00-5, Rdea594, Rdea 594, Zurampic, Rdea-594, 2-((5-bromo-4-(4-cyclopropylnaphthalen-1-yl)-4h-1,2,4-triazol-3-yl)thio)acetic acid
Molecular Formula
C17H14BrN3O2S
Molecular Weight
404.3  g/mol
InChI Key
FGQFOYHRJSUHMR-UHFFFAOYSA-N
FDA UNII
73WY698HZ7

Lesinurad
Lesinurad is an oral uric acid transporter 1 (URAT1) inhibitor indicated for the treatment of hyperuricemia associated with gout. It reduces serum uric acid concentration through the inhibition of URAT1, an enzyme responsible for reuptake of uric acid from the renal tubule, and OAT4, another uric acid transporter associated with diuretic-induced hyperuricemia. Marketed as the product Zurampic, it is indicated for use in combination with a xanthine oxidase inhibitor for the treatment of hyperuricemia associated with gout in patients who have not achieved target serum uric acid levels with a xanthine oxidase inhibitor alone. In August 2017, a combination oral therapy consisting of lesinurad and [DB00437] was FDA-approved under the brand name Duzallo indicated for the treatment of gout-related hyperuricemia in patients with uncontrolled gout.
Lesinurad is an Urate Transporter 1 Inhibitor. The mechanism of action of lesinurad is as an Urate Transporter 1 Inhibitor, and Cytochrome P450 3A Inducer.
1 2D Structure

Lesinurad

2 Identification
2.1 Computed Descriptors
2.1.1 IUPAC Name
2-[[5-bromo-4-(4-cyclopropylnaphthalen-1-yl)-1,2,4-triazol-3-yl]sulfanyl]acetic acid
2.1.2 InChI
InChI=1S/C17H14BrN3O2S/c18-16-19-20-17(24-9-15(22)23)21(16)14-8-7-11(10-5-6-10)12-3-1-2-4-13(12)14/h1-4,7-8,10H,5-6,9H2,(H,22,23)
2.1.3 InChI Key
FGQFOYHRJSUHMR-UHFFFAOYSA-N
2.1.4 Canonical SMILES
C1CC1C2=CC=C(C3=CC=CC=C23)N4C(=NN=C4Br)SCC(=O)O
2.2 Other Identifiers
2.2.1 UNII
73WY698HZ7
2.3 Synonyms
2.3.1 MeSH Synonyms

1. ((5-bromo-4-(4-cyclopropyl-1-naphthyl)-4h-1,2,4-triazol-3-yl)sulfanyl)acetic Acid

2. Rdea594

3. Zurampic

2.3.2 Depositor-Supplied Synonyms

1. 878672-00-5

2. Rdea594

3. Rdea 594

4. Zurampic

5. Rdea-594

6. 2-((5-bromo-4-(4-cyclopropylnaphthalen-1-yl)-4h-1,2,4-triazol-3-yl)thio)acetic Acid

7. Lesinurad Free Acid

8. (+)-lesinurad

9. (-)-lesinurad

10. Lesinurad, (+)-

11. Lesinurad, (-)-

12. Lesinurad, (4r)-

13. Lesinurad, (4s)-

14. Q59cat99rs

15. 09erp08i3w

16. 73wy698hz7

17. 878672-00-5 (free Acid)

18. 2-(5-bromo-4-(4-cyclopropylnaphthalen-1-yl)-4h-1,2,4-triazol-3-ylthio)acetic Acid

19. 2-[[5-bromo-4-(4-cyclopropylnaphthalen-1-yl)-1,2,4-triazol-3-yl]sulfanyl]acetic Acid

20. 2-[[5-bromo-4-(4-cyclopropylnaphthalen-1-yl)-4h-1,2,4-triazol-3-yl]thio]acetic Acid

21. {[5-bromo-4-(4-cyclopropylnaphthalen-1-yl)-4h-1,2,4-triazol-3-yl]sulfanyl}acetic Acid

22. 2-(((4r)-5-bromo-4-(4-cyclopropyl-1-naphthalenyl)-4h-1,2,4-triazol-3-yl)thio)acetic Acid

23. 2-(((4s)-5-bromo-4-(4-cyclopropyl-1-naphthalenyl)-4h-1,2,4-triazol-3-yl)thio)acetic Acid

24. 2-{[5-bromo-4-(4-cyclopropylnaphthalen-1-yl)-4h-1,2,4-triazol-3-yl]sulfanyl}acetic Acid

25. Acetic Acid, 2-((5-bromo-4-(4-cyclopropyl-1-naphthalenyl)-4h-1,2,4-triazol-3-yl)thio)-

26. 1890222-25-9

27. 1890222-26-0

28. Acetic Acid, 2-(((4r)-5-bromo-4-(4-cyclopropyl-1-naphthalenyl)-4h-1,2,4-triazol-3-yl)thio)-

29. Acetic Acid, 2-(((4s)-5-bromo-4-(4-cyclopropyl-1-naphthalenyl)-4h-1,2,4-triazol-3-yl)thio)-

30. Lesinurad [usan]

31. Lesinurad [usan:inn]

32. Unii-09erp08i3w

33. Zurampic (tn)

34. Lesinurad (rdea594

35. Lesinurad [inn]

36. Lesinurad [mi]

37. Lesinurad (usan/inn)

38. Lesinurad (rdea594)

39. Unii-q59cat99rs

40. Lesinurad [who-dd]

41. Schembl842962

42. Unii-73wy698hz7

43. Gtpl7673

44. Lesinurad [orange Book]

45. Chembl2105720

46. Lesinurad, >=98% (hplc)

47. Bdbm37953

48. Chebi:90929

49. Duzallo Component Lesinurad

50. Dtxsid201026091

51. Hms3874m03

52. Amy27876

53. Bcp06435

54. Ex-a1289

55. Us10093631, Compound Lesinurad

56. Mfcd22572730

57. S4640

58. Zinc84757007

59. Akos027327368

60. Ccg-268685

61. Cs-1389

62. Db11560

63. Sb16705

64. Ac-29310

65. As-56014

66. Hy-15258

67. Rdea 594;rdea-594;rdea594

68. Ft-0776044

69. D09921

70. A857828

71. Q21820633

72. (5-bromo-4-(1-cyclopropylnaphthalen-4-yl)-4h-1,2,4-triazol-3-ylthio)acetic Acid

73. 2-(5-bromo-4-(1-cyclopropylnaphthalen-4-yl)-4h-1,2,4-triazol-3-ylthio)acetic Acid

74. 2-[[5-bromo-4-(4-cyclopropyl-1-naphthalenyl)-4h-1,2,4-triazol-3-yl]thio]-acetic Acid

75. 2-((5-bromo-4-(4-cyclopropylnaphthalen-1-yl)-4h-1,2,4-triazol-3- Yl)sulfanyl)acetic Acid

76. Rdea 594;sodium 2-((5-bromo-4-(4-cyclopropylnaphthalen-1-yl)-4h-1,2,4-triazol-3-yl)thio)acetate

2.4 Create Date
2011-10-31
3 Chemical and Physical Properties
Molecular Weight 404.3 g/mol
Molecular Formula C17H14BrN3O2S
XLogP34.7
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count5
Rotatable Bond Count5
Exact Mass402.99901 g/mol
Monoisotopic Mass402.99901 g/mol
Topological Polar Surface Area93.3 Ų
Heavy Atom Count24
Formal Charge0
Complexity479
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently Bonded Unit Count1
4 Drug and Medication Information
4.1 Drug Indication

For use, in combination with a xanthine oxidase inhibitor, for the treatment of hyperuricemia associated with gout in patients who have not achieved target serum uric acid levels with a xanthine oxidase inhibitor alone.


FDA Label


Zurampic, in combination with a xanthine oxidase inhibitor, is indicated in adults for the adjunctive treatment of hyperuricaemia in gout patients (with or without tophi) who have not achieved target serum uric acid levels with an adequate dose of a xanthine oxidase inhibitor alone.


5 Pharmacology and Biochemistry
5.1 Pharmacology

Dose-dependent reductions in serum uric acid levels and increases in urinary uric acid excretion have been observed following single and multiple oral doses of lesinurad.


5.2 MeSH Pharmacological Classification

Gout Suppressants

Agents that increase uric acid excretion by the kidney (URICOSURIC AGENTS), decrease uric acid production (antihyperuricemics), or alleviate the pain and inflammation of acute attacks of gout. (See all compounds classified as Gout Suppressants.)


Uricosuric Agents

Gout suppressants that act directly on the renal tubule to increase the excretion of uric acid, thus reducing its concentrations in plasma. (See all compounds classified as Uricosuric Agents.)


5.3 FDA Pharmacological Classification
5.3.1 Active Moiety
LESINURAD
5.3.2 FDA UNII
09ERP08I3W
5.3.3 Pharmacological Classes
Mechanisms of Action [MoA] - Cytochrome P450 3A Inducers
5.4 ATC Code

M04AB05


M - Musculo-skeletal system

M04 - Antigout preparations

M04A - Antigout preparations

M04AB - Preparations increasing uric acid excretion

M04AB05 - Lesinurad


5.5 Absorption, Distribution and Excretion

Absorption

Oral lesinurad is rapidly absorbed, reaching maximum plasma concentrations (Cmax) within 14 h following the administration a single 200 mg dose (in either the fed or fasted state).


Route of Elimination

Within 7 days following single dosing of radiolabeled lesinurad, 63% of administered radioactive dose was recovered in urine and 32% of administered radioactive dose was recovered in feces. Most of the radioactivity recovered in urine (> 60% of dose) occurred in the first 24 hours. Unchanged lesinurad in urine accounted for approximately 30% of the dose.


Volume of Distribution

The mean steady state volume of distribution of lesinurad was approximately 20 L following intravenous dosing.


5.6 Metabolism/Metabolites

Lesinurad undergoes oxidative metabolism mainly via the polymorphic cytochrome P450 CYP2C9 enzyme.


5.7 Mechanism of Action

Lesinurad inhibits the activity of uric acid transporter 1 (URAT1) and organic anion transporter 4 (OAT4). URAT1 is a major transporter enzyme responsible for reuptake of uric acid from the renal tubules; inhibition of URAT1 function thereby increases excretion of uric acid.


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DOSAGE - TABLET;ORAL - 200MG

USFDA APPLICATION NUMBER - 207988

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DOSAGE - TABLET;ORAL - 200MG;200MG

USFDA APPLICATION NUMBER - 209203

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DOSAGE - TABLET;ORAL - 300MG;200MG

USFDA APPLICATION NUMBER - 209203

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ABOUT THIS PAGE

Lesinurad Manufacturers

A Lesinurad manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lesinurad, including repackagers and relabelers. The FDA regulates Lesinurad manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lesinurad API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.

click here to find a list of Lesinurad manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

Lesinurad Suppliers

A Lesinurad supplier is an individual or a company that provides Lesinurad active pharmaceutical ingredient (API) or Lesinurad finished formulations upon request. The Lesinurad suppliers may include Lesinurad API manufacturers, exporters, distributors and traders.

click here to find a list of Lesinurad suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Lesinurad USDMF

A Lesinurad DMF (Drug Master File) is a document detailing the whole manufacturing process of Lesinurad active pharmaceutical ingredient (API) in detail. Different forms of Lesinurad DMFs exist exist since differing nations have different regulations, such as Lesinurad USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A Lesinurad DMF submitted to regulatory agencies in the US is known as a USDMF. Lesinurad USDMF includes data on Lesinurad's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Lesinurad USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of Lesinurad suppliers with USDMF on PharmaCompass.

Lesinurad NDC

National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Lesinurad as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Lesinurad API and other APIs are published in this directory by the FDA.

Unfinished drugs

The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.

Pharmaceutical companies that manufacture Lesinurad as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.

Compounded drug products

The NDC directory also contains data on finished compounded human drug products that contain Lesinurad and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Lesinurad NDC to their finished compounded human drug products, they may choose to do so.

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Lesinurad GMP

Lesinurad Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.

GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).

PharmaCompass offers a list of Lesinurad GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right Lesinurad GMP manufacturer or Lesinurad GMP API supplier for your needs.

Lesinurad CoA

A Lesinurad CoA (Certificate of Analysis) is a formal document that attests to Lesinurad's compliance with Lesinurad specifications and serves as a tool for batch-level quality control.

Lesinurad CoA mostly includes findings from lab analyses of a specific batch. For each Lesinurad CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.

Lesinurad may be tested according to a variety of international standards, such as European Pharmacopoeia (Lesinurad EP), Lesinurad JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Lesinurad USP).

Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.
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