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Chemistry

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Also known as: 775304-57-9, Ptc124, 3-(5-(2-fluorophenyl)-1,2,4-oxadiazol-3-yl)benzoic acid, 3-[5-(2-fluorophenyl)-1,2,4-oxadiazol-3-yl]benzoic acid, Ptc-124, Ataluren (ptc124)
Molecular Formula
C15H9FN2O3
Molecular Weight
284.24  g/mol
InChI Key
OOUGLTULBSNHNF-UHFFFAOYSA-N
FDA UNII
K16AME9I3V

Ataluren
Ataluren is a novel, orally administered drug that targets nonsense mutations. Ataluren is approved for use by the European Medicines Agency to treat Duchenne Muscular Dystrophy in patients aged 5 years and older who are able to walk. More specifically, ataluren is used in the small group of patients whose disease is caused by a specific genetic defect (called a nonsense mutation) in the dystrophin gene. This drug does not yet have approval by the US Food and Drug Administration or by Health Canada for any indications.
1 2D Structure

Ataluren

2 Identification
2.1 Computed Descriptors
2.1.1 IUPAC Name
3-[5-(2-fluorophenyl)-1,2,4-oxadiazol-3-yl]benzoic acid
2.1.2 InChI
InChI=1S/C15H9FN2O3/c16-12-7-2-1-6-11(12)14-17-13(18-21-14)9-4-3-5-10(8-9)15(19)20/h1-8H,(H,19,20)
2.1.3 InChI Key
OOUGLTULBSNHNF-UHFFFAOYSA-N
2.1.4 Canonical SMILES
C1=CC=C(C(=C1)C2=NC(=NO2)C3=CC(=CC=C3)C(=O)O)F
2.2 Other Identifiers
2.2.1 UNII
K16AME9I3V
2.3 Synonyms
2.3.1 MeSH Synonyms

1. Ptc 124

2. Ptc-124

3. Ptc124

2.3.2 Depositor-Supplied Synonyms

1. 775304-57-9

2. Ptc124

3. 3-(5-(2-fluorophenyl)-1,2,4-oxadiazol-3-yl)benzoic Acid

4. 3-[5-(2-fluorophenyl)-1,2,4-oxadiazol-3-yl]benzoic Acid

5. Ptc-124

6. Ataluren (ptc124)

7. Translarna

8. Ptc124 (ataluren)

9. Ptc 124

10. Benzoic Acid, 3-[5-(2-fluorophenyl)-1,2,4-oxadiazol-3-yl]-

11. K16ame9i3v

12. Ncgc00168759-02

13. Benzoic Acid, 3-(5-(2-fluorophenyl)-1,2,4-oxadiazol-3-yl)-

14. Dsstox_cid_26776

15. Dsstox_rid_81895

16. Dsstox_gsid_46776

17. Ataluren [usan]

18. Cas-775304-57-9

19. Ataluren [usan:inn]

20. Unii-k16ame9i3v

21. Translarna (tn)

22. Ptc124,ataluren

23. Ataluren(ptc124)

24. Ataluren; Ptc124

25. Ptc124 - Ataluren

26. Ataluren (usan/inn)

27. Ataluren [inn]

28. Ataluren [mi]

29. Ec-000.2051

30. Ataluren [who-dd]

31. Schembl60614

32. Mls006011160

33. Chembl256997

34. Gtpl7341

35. Dtxsid5046776

36. Chebi:94805

37. Ex-a385

38. Bcpp000097

39. Hms3656h20

40. Albb-036381

41. Bcp01756

42. Tox21_112631

43. Bbl102158

44. Mfcd09864996

45. Ncgc00168759

46. S6003

47. Stl555957

48. Zinc13831791

49. Akos005146455

50. Tox21_112631_1

51. Ccg-267286

52. Cs-0503

53. Db05016

54. Ex-3387

55. Gs-3946

56. Sb16685

57. Ncgc00168759-04

58. Ncgc00168759-05

59. Ncgc00168759-10

60. Ac-28390

61. Am808091

62. Hy-14832

63. Smr004702931

64. Bb 0261439

65. Ft-0651455

66. Sw219696-1

67. D09323

68. 304f579

69. Au-004/43508117

70. Q753330

71. Brd-k94830329-001-01-4

72. 3-[5-(2-fluoro-phenyl)-[1,2,4]oxadiazol-3-yl]-benzoic Acid

73. 3-[5-(2-fluorophenyl)-[1,2,4]oxadiazol-3-yl]benzoic Acid

74. Ptc124;3-[5-(2-fluorophenyl)-1,2,4-oxadiazol-3-yl]benzoic Acid;ptc-124

75. Jbf

2.4 Create Date
2006-10-26
3 Chemical and Physical Properties
Molecular Weight 284.24 g/mol
Molecular Formula C15H9FN2O3
XLogP33.1
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count6
Rotatable Bond Count3
Exact Mass284.05972032 g/mol
Monoisotopic Mass284.05972032 g/mol
Topological Polar Surface Area76.2 Ų
Heavy Atom Count21
Formal Charge0
Complexity382
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

Ataluren is approved for use by the European Medicines Agency to treat Duchenne Muscular Dystrophy in patients aged 5 years and older who are able to walk. More specifically, ataluren is used in the small group of patients whose disease is caused by a specific genetic defect (called a nonsense mutation) in the dystrophin gene.


Translarna is indicated for the treatment of Duchenne muscular dystrophy resulting from a nonsense mutation in the dystrophin gene, in ambulatory patients aged 2 years and older. Efficacy has not been demonstrated in non-ambulatory patients.

The presence of a nonsense mutation in the dystrophin gene should be determined by genetic testing.


Treatment of cystic fibrosis


Treatment of dystrophinopathy


5 Pharmacology and Biochemistry
5.1 ATC Code

M09AX03


M - Musculo-skeletal system

M09 - Other drugs for disorders of the musculo-skeletal system

M09A - Other drugs for disorders of the musculo-skeletal system

M09AX - Other drugs for disorders of the musculo-skeletal system

M09AX03 - Ataluren


5.2 Absorption, Distribution and Excretion

Absorption

Peak plasma levels of ataluren are attained approximately 1.5 hours after dosing in subjects who received medicinal product within 30 minutes of a meal.


Route of Elimination

After a single oral dose of radiolabeled ataluren, approximately half of the administered radioactive dose is recovered in the faeces and the remainder was recovered in the urine. In the urine, unchanged ataluren and the acyl glucuronide metabolite account for less than 1% and 49%, respectively, of the administered dose.


5.3 Metabolism/Metabolites

Ataluren is metabolized by conjugation via uridine diphosphate glucuronosyltransferase (UGT) enzymes, predominantly UGT1A9 in liver and intestine. In vivo, the only metabolite detected in plasma after oral administration of radio-labelled ataluren was the ataluren-O-1-acyl glucuronide; exposure to this metabolite in humans was approximately 8% of the plasma AUC of ataluren.


5.4 Biological Half-Life

Ataluren plasma half-life ranges from 2-6 hours and is unaffected either by dose or repeated administration.


5.5 Mechanism of Action

Ataluren enables ribosomal readthrough of mRNA containing premature stop codons that otherwise would result in premature termination of protein chains. Use of ataluren allows cellular machinery to bypass nonsense mutations in genetic material, continue the translation process, and thereby restore the production of a full-length, functional protein. The research on the effects of Ataluren on the translation and stability of nonsense-containing mRNA in vitor show that Ataluren promoted readthrough at each of the nonsense codons, showing maximal activity with UGA, while having no effect on mRNA levels. Unlike the stable cell line assays, Ataluren did not discriminate significantly between the UAG and UAA mRNAs. Ataluren was a more potent nonsense-suppressing agent than gentamicin, and exhibited 4- to 15-fold stimulation of in vitro readthrough relative to the controls at levels similar to those in the stable cell reporter assays. These results indicate that Ataluren modulates termination efficiency at premature nonsense codons.


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Lifecare Laboratories Pvt Ltd

India

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Virtual BoothLifecare Labs has been developing innovative products in specialist areas of medicine.

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NDC API

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ASC 2024
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ATALUREN

NDC Package Code : 48087-0138

Start Marketing Date : 2018-11-29

End Marketing Date : 2024-12-31

Dosage Form (Strength) : POWDER (1kg/kg)

Marketing Category : BULK INGREDIENT

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Virtual BoothLifecare Labs has been developing innovative products in specialist areas of medicine.

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Ataluren

About the Company : Lifecare Labs specializes in producing bulk drugs (APIs) and intermediates that adhere to the industry's stringent quality parameters. Its objective is to deliver excellence throug...

Lifecare Labs specializes in producing bulk drugs (APIs) and intermediates that adhere to the industry's stringent quality parameters. Its objective is to deliver excellence through its "quality designed for excellence" mission and meet its customers' requirements. Cost-effectiveness is a top priority for the company, and it aims to establish long-term relationships with its clients. Lifecare Labs possesses state-of-the-art facilities for manufacturing bulk drugs (APIs) and intermediates and has dedicated units for products. Its mission is to become a globally recognized company responsible for its customers, business partners and society.
LifeCare Laboratories
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API Reference Price

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18-Oct-2022
18-Oct-2022
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