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1. 2-(2-nitro-4-(trifluoromethyl)benzoyl)cyclohexane-1,3-dione
2. 2-(2-nitro-4-trifluoromethylbenzoyl)-1,3-cyclohexanedione
3. Ntbc Cpd
4. Orfadin
1. 104206-65-7
2. Orfadin
3. 2-(2-nitro-4-(trifluoromethyl)benzoyl)cyclohexane-1,3-dione
4. Nitisone
5. Ntbc
6. 2-(2-nitro-4-trifluoromethylbenzoyl)-1,3-cyclohexanedione
7. 2-[2-nitro-4-(trifluoromethyl)benzoyl]cyclohexane-1,3-dione
8. 2-(2-nitro-4-trifluoromethylbenzoyl)cyclohexane-1,3-dione
9. Sc 0735
10. Sc-0735
11. 2-(alpha,alpha,alpha-trifluoro-2-nitro-p-tuluoyl)-1,3-cyclohexanedione
12. 1,3-cyclohexanedione, 2-[2-nitro-4-(trifluoromethyl)benzoyl]-
13. 2-{[2-nitro-4-(trifluoromethyl)phenyl]carbonyl}cyclohexane-1,3-dione
14. Chembl1337
15. Chebi:50378
16. 1,3-cyclohexanedione, 2-(2-nitro-4-(trifluoromethyl)benzoyl)-
17. Mfcd01752192
18. Sc0735
19. K5bn214699
20. Nitisinone [inn]
21. Nitisinone [usan:inn]
22. Nitisinona
23. Nitisinonum
24. Smr002529592
25. Orfadin (tn)
26. Nitisinone (jan/usan/inn)
27. Unii-k5bn214699
28. Nityr
29. Fe-0200
30. 2-[2-nitro-4-(trifluoromethyl)benzoyl]-1,3-cyclohexanedione
31. Nitisinone [mi]
32. Nitisinone [jan]
33. Nitisinone [usan]
34. Nitisinone [vandf]
35. Nitisinone [mart.]
36. Nitisinone [who-dd]
37. Bidd:pxr0129
38. Mls004774025
39. Mls006011955
40. Nitisinone [ema Epar]
41. Schembl338795
42. Ambz0071
43. Gtpl6834
44. Dtxsid9042673
45. Nitisinone [orange Book]
46. Nitisinone, >=95% (hplc)
47. Schembl15996621
48. Hms3740a15
49. Hms3870k03
50. Bcp15276
51. Hy-b0607
52. Bdbm50088804
53. Nsc773149
54. Rb3134
55. S5325
56. Akos015891363
57. Akos015994590
58. Zinc100014475
59. Am62666
60. Ccg-222085
61. Db00348
62. Ex-6233
63. Nsc-773149
64. Sb19017
65. Ncgc00185778-01
66. Ncgc00185778-02
67. Ncgc00185778-04
68. Ncgc00185778-07
69. Ac-26934
70. Sy047291
71. Db-014936
72. Ft-0672739
73. D05177
74. A800922
75. Sr-01000940576
76. J-505680
77. Q3877355
78. Sr-01000940576-2
79. Ntbc; Nitisone; Sc0735; Sc 0735; Sc-0735
80. Z1514110653
81. 1,3-cyclohexanedione,2-[2-nitro-4-(trifluoromethyl)benzoyl]-
82. 2-(2-nitro-4-(trifluoromethyl)-benzoyl)cyclohexane-1,3-dione
83. 2-[2-nitro-4-(trifluoromethyl)benzoyl]cyclohexane-1,3-dione;nitisinone
84. 2-(.alpha.,.alpha.,.alpha.-trifluoro-2-nitro-p-tuluoyl)-1,3-cyclohexanedione
Molecular Weight | 329.23 g/mol |
---|---|
Molecular Formula | C14H10F3NO5 |
XLogP3 | 2.3 |
Hydrogen Bond Donor Count | 0 |
Hydrogen Bond Acceptor Count | 8 |
Rotatable Bond Count | 2 |
Exact Mass | 329.05110691 g/mol |
Monoisotopic Mass | 329.05110691 g/mol |
Topological Polar Surface Area | 97 Ų |
Heavy Atom Count | 23 |
Formal Charge | 0 |
Complexity | 524 |
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 |
1 of 2 | |
---|---|
Drug Name | Orfadin |
PubMed Health | Nitisinone (By mouth) |
Drug Classes | Gastrointestinal Agent |
Drug Label | Orfadin contains nitisinone, which is a hydroxyphenyl-pyruvate dioxygenase inhibitor indicated as an adjunct to dietary restriction of tyrosine and phenylalanine in the treatment of hereditary tyrosinemia type 1 (HT-1). Nitisinone occurs as white to... |
Active Ingredient | Nitisinone |
Dosage Form | Capsule |
Route | Oral |
Strength | 5mg; 2mg; 10mg |
Market Status | Prescription |
Company | Swedish Orphan |
2 of 2 | |
---|---|
Drug Name | Orfadin |
PubMed Health | Nitisinone (By mouth) |
Drug Classes | Gastrointestinal Agent |
Drug Label | Orfadin contains nitisinone, which is a hydroxyphenyl-pyruvate dioxygenase inhibitor indicated as an adjunct to dietary restriction of tyrosine and phenylalanine in the treatment of hereditary tyrosinemia type 1 (HT-1). Nitisinone occurs as white to... |
Active Ingredient | Nitisinone |
Dosage Form | Capsule |
Route | Oral |
Strength | 5mg; 2mg; 10mg |
Market Status | Prescription |
Company | Swedish Orphan |
Used as an adjunct to dietary restriction of tyrosine and phenylalanine in the treatment of hereditary tyrosinemia type 1.
FDA Label
Hereditary tyrosinemia type 1 (HT 1)
Orfadin is indicated for the treatment of adult and paediatric (in any age range) patients with confirmed diagnosis of hereditary tyrosinemia type 1 (HT 1) in combination with dietary restriction of tyrosine and phenylalanine.
Alkaptonuria (AKU)
Orfadin is indicated for the treatment of adult patients with alkaptonuria (AKU).
Treatment of adult and paediatric patients with confirmed diagnosis of hereditary tyrosinemia type 1 (HT-1) in combination with dietary restriction of tyrosine and phenylalanine.
Treatment of adult and paediatric (in any age range) patients with confirmed diagnosis of hereditary tyrosinemia type 1 (HT 1) in combination with dietary restriction of tyrosine and phenylalanine.
Treatment of tyrosinemia type 1
Hereditary tyrosinemia type 1 occurs due to a deficiency in fumarylacetoacetase (FAH), the final enzyme in the tyrosine catabolic pathway. Nitisinone inhibits catabolism of tyrosine by preventing the catabolic intermediates. In patients with HT-1, these catabolic intermediates are converted to the toxic metabolites succinylacetone and succinylacetoacetate, which are responsible for the observed liver and kidney toxicity. Succinylacetone can also inhibit the porphyrin synthesis pathway leading to the accumulation of 5-aminolevulinate, a neurotoxin responsible for the porphyric crises characteristic of HT-1.
Enzyme Inhibitors
Compounds or agents that combine with an enzyme in such a manner as to prevent the normal substrate-enzyme combination and the catalytic reaction. (See all compounds classified as Enzyme Inhibitors.)
A16AX04
A16AX04
A16AX04
A - Alimentary tract and metabolism
A16 - Other alimentary tract and metabolism products
A16A - Other alimentary tract and metabolism products
A16AX - Various alimentary tract and metabolism products
A16AX04 - Nitisinone
Absorption
The capsule and liquid formulations are bioequivalent in both the plasma concentration-time curve and maximum plasma concentration (Cmax).
~54 hours
Nitisinone is a competitive inhibitor of 4-hydroxyphenyl-pyruvate dioxygenase, an enzyme upstream of fumarylacetoacetate hydrolyase (FAH) in the tyrosine catabolic pathway. By inhibiting the normal catabolism of tyrosine in patients with hereditary tyrosinemia type 1 (HT-1), nitisinone prevents the accumulation of the catabolic intermediates maleylacetoacetate and fumarylacetoacetate.
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PharmaCompass offers a list of Nitisinone API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Nitisinone manufacturer or Nitisinone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Nitisinone manufacturer or Nitisinone supplier.
PharmaCompass also assists you with knowing the Nitisinone API Price utilized in the formulation of products. Nitisinone API Price is not always fixed or binding as the Nitisinone Price is obtained through a variety of data sources. The Nitisinone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Orfadin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Orfadin, including repackagers and relabelers. The FDA regulates Orfadin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Orfadin 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 Orfadin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Orfadin supplier is an individual or a company that provides Orfadin active pharmaceutical ingredient (API) or Orfadin finished formulations upon request. The Orfadin suppliers may include Orfadin API manufacturers, exporters, distributors and traders.
click here to find a list of Orfadin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Orfadin DMF (Drug Master File) is a document detailing the whole manufacturing process of Orfadin active pharmaceutical ingredient (API) in detail. Different forms of Orfadin DMFs exist exist since differing nations have different regulations, such as Orfadin USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Orfadin DMF submitted to regulatory agencies in the US is known as a USDMF. Orfadin USDMF includes data on Orfadin's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Orfadin USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Orfadin suppliers with USDMF on PharmaCompass.
A Orfadin written confirmation (Orfadin WC) is an official document issued by a regulatory agency to a Orfadin manufacturer, verifying that the manufacturing facility of a Orfadin active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Orfadin APIs or Orfadin finished pharmaceutical products to another nation, regulatory agencies frequently require a Orfadin WC (written confirmation) as part of the regulatory process.
click here to find a list of Orfadin suppliers with Written Confirmation (WC) 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 Orfadin as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Orfadin 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 Orfadin 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 Orfadin and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Orfadin NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Orfadin suppliers with NDC on PharmaCompass.
Orfadin 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 Orfadin 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 Orfadin GMP manufacturer or Orfadin GMP API supplier for your needs.
A Orfadin CoA (Certificate of Analysis) is a formal document that attests to Orfadin's compliance with Orfadin specifications and serves as a tool for batch-level quality control.
Orfadin CoA mostly includes findings from lab analyses of a specific batch. For each Orfadin 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.
Orfadin may be tested according to a variety of international standards, such as European Pharmacopoeia (Orfadin EP), Orfadin JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Orfadin USP).