Introduction:Basic information about CAS 104206-65-7|Nitisinone, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
| Common Name | Nitisinone |
|---|
| CAS Number | 104206-65-7 | Molecular Weight | 329.228 |
|---|
| Density | 1.5±0.1 g/cm3 | Boiling Point | 486.2±45.0 °C at 760 mmHg |
|---|
| Molecular Formula | C14H10F3NO5 | Melting Point | 129-131°C |
|---|
| MSDS | ChineseUSA | Flash Point | 247.9±28.7 °C |
|---|
Names
| Name | nitisinone |
|---|
| Synonym | More Synonyms |
|---|
Nitisinone BiologicalActivity
| Description | Nitisinone(SC0735) is an inhibitor of the enzyme 4-hydroxyphenylpyruvate dioxygenase.Target: 4-Hydroxyphenylpyruvate DioxygenaseNitisinone is a drug used to slow the effects of hereditary tyrosinemia type 1. Nitisinone reduced urinary HGA levels from an average of 4.0 +/- 1.8 (SD) g/day to 0.2 +/- 0.2 g/day ( P < .001). Low-dose nitisinone effectively reduced urinary HGA levels in patients with alkaptonuria. Future long-term clinical trials are planned to determine the benefits of nitisinone in preventing joint deterioration and providing pain relief, and its long-term side effects [1]. Nitisinone can prevent the development of liver disease and significantly reduce the risk of developing hepatocellular carcinoma; however, vigorous surveillance for the development of HCC needs to be continued lifelong [2]. |
|---|
| Related Catalog | Signaling Pathways >>Others >>OthersResearch Areas >>Metabolic Disease |
|---|
| References | [1]. Suwannarat, P., et al., Use of nitisinone in patients with alkaptonuria. Metabolism, 2005. 54(6): p. 719-28. [2]. Santra, S. and U. Baumann, Experience of nitisinone for the pharmacological treatment of hereditary tyrosinaemia type 1. Expert Opin Pharmacother, 2008. 9(7): p. 1229-36. |
|---|
Chemical & Physical Properties
| Density | 1.5±0.1 g/cm3 |
|---|
| Boiling Point | 486.2±45.0 °C at 760 mmHg |
|---|
| Melting Point | 129-131°C |
|---|
| Molecular Formula | C14H10F3NO5 |
|---|
| Molecular Weight | 329.228 |
|---|
| Flash Point | 247.9±28.7 °C |
|---|
| Exact Mass | 329.051117 |
|---|
| PSA | 97.03000 |
|---|
| LogP | 1.37 |
|---|
| Vapour Pressure | 0.0±1.2 mmHg at 25°C |
|---|
| Index of Refraction | 1.535 |
|---|
| InChIKey | OUBCNLGXQFSTLU-UHFFFAOYSA-N |
|---|
| SMILES | O=C1CCCC(=O)C1C(=O)c1ccc(C(F)(F)F)cc1[N+](=O)[O-] |
|---|
| Storage condition | 2-8°C |
|---|
Toxicological Information
CHEMICAL IDENTIFICATION - RTECS NUMBER :
- GV0766666
- CHEMICAL NAME :
- 1,3-Cyclohexanedione, 2-(2-nitro-4-trifluorobenzoyl)-
- CAS REGISTRY NUMBER :
- 104206-65-7
- LAST UPDATED :
- 199806
- DATA ITEMS CITED :
- 1
HEALTH HAZARD DATAACUTE TOXICITY DATA - TYPE OF TEST :
- TDLo - Lowest published toxic dose
- ROUTE OF EXPOSURE :
- Oral
- SPECIES OBSERVED :
- Rodent - rat
- DOSE/DURATION :
- 4200 ug/kg/6W-I
- TOXIC EFFECTS :
- Sense Organs and Special Senses (Eye) - corneal damage Blood - other changes
- REFERENCE :
- TXAPA9 Toxicology and Applied Pharmacology. (Academic Press, Inc., 1 E. First St., Duluth, MN 55802) V.1- 1959- Volume(issue)/page/year: 141,439,1996
|
Safety Information
| Hazard Codes | Xi |
|---|
| RIDADR | NONH for all modes of transport |
|---|
| HS Code | 2914700090 |
|---|
Customs
| HS Code | 2914700090 |
|---|
| Summary | HS: 2914700090 halogenated, sulphonated, nitrated or nitrosated derivatives of ketones and quinones, whether or not with other oxygen function Tax rebate rate:9.0% Supervision conditions:none VAT:17.0% MFN tariff:5.5% General tariff:30.0% |
|---|
Articles29
More Articles
| Generation of healthy mice from gene-corrected disease-specific induced pluripotent stem cells. PLoS Biol. 9(7) , e1001099, (2011) Using the murine model of tyrosinemia type 1 (fumarylacetoacetate hydrolase [FAH] deficiency; FAH⁻/⁻ mice) as a paradigm for orphan disorders, such as hereditary metabolic liver diseases, we evaluated... | |
| Serum markers in alkaptonuria: simultaneous analysis of homogentisic acid, tyrosine and nitisinone by liquid chromatography tandem mass spectrometry. Ann. Clin. Biochem. 52 , 597-605, (2015) Alkaptonuria is a rare debilitating autosomal recessive disorder of tyrosine metabolism, where deficiency of homogentisate 1,2-dioxygenase results in increased homogentisic acid. Homogentisic acid is ... | |
| A misguided 'pill in the pocket' approach with flecainide leading to cardiac arrest. BMJ Case Rep. 2012 , doi:10.1136/bcr-2012-006868, (2012)
| |
Synonyms
| nitisinonum |
| 2-(2-Nitro-4-trifluoromethylbenzoyl)-1,3-cyclohexanedione |
| 2-[2-Nitro-4-(trifluoromethyl)benzoyl]-1,3-cyclohexanedione |
| 2-(2-nitro-4-(trifluoromethyl)benzoyl)cyclohexane-1,3-dione |
| Orfadin |
| Nitisinone [INN] |
| nitisinona |
| Orfadin (TN) |
| 1,3-Cyclohexanedione, 2-[2-nitro-4-(trifluoromethyl)benzoyl]- |
| Nitisone |
| 2-(2-Nitro-4-trifluoromethylbenzoyl)cyclohexane-1,3-dione |
| 2-[2-nitro-4-(trifluoromethyl)benzoyl]cyclohexane-1,3-dione |
| Nitisinone |