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1. ((5-bromo-4-(4-cyclopropyl-1-naphthyl)-4h-1,2,4-triazol-3-yl)sulfanyl)acetic Acid
2. Rdea594
3. Zurampic
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
Molecular Weight | 404.3 g/mol |
---|---|
Molecular Formula | C17H14BrN3O2S |
XLogP3 | 4.7 |
Hydrogen Bond Donor Count | 1 |
Hydrogen Bond Acceptor Count | 5 |
Rotatable Bond Count | 5 |
Exact Mass | 402.99901 g/mol |
Monoisotopic Mass | 402.99901 g/mol |
Topological Polar Surface Area | 93.3 Ų |
Heavy Atom Count | 24 |
Formal Charge | 0 |
Complexity | 479 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 0 |
Undefined Atom Stereocenter Count | 0 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 1 |
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.
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.
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.)
M04AB05
M - Musculo-skeletal system
M04 - Antigout preparations
M04A - Antigout preparations
M04AB - Preparations increasing uric acid excretion
M04AB05 - Lesinurad
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.
Lesinurad undergoes oxidative metabolism mainly via the polymorphic cytochrome P450 CYP2C9 enzyme.
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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ABOUT THIS PAGE
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.
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.
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.
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).
The FDA updates the NDC directory daily. The NDC numbers for Lesinurad API and other APIs are published in this directory by the FDA.
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.
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.
click here to find a list of Lesinurad suppliers with NDC on PharmaCompass.
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.
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).
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