Deferasirox
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Systematic (IUPAC) name | |
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[4-[(3Z,5E)-3,5-bis(6-oxo-1-cyclohexa-2,4- dienylidene)-1,2,4-triazolidin-1-yl]benzoic acid | |
Clinical data | |
[[Regulation of therapeutic goods |Template:Engvar data]] |
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Pregnancy category | |
Routes of administration | Oral |
Legal status | |
Legal status | |
Pharmacokinetic data | |
Bioavailability | 70% |
Protein binding | 99% |
Metabolism | Hepatic glucuronidation |
Biological half-life | 8 to 16 hours |
Excretion | Fecal (84%) and renal (8%) |
Identifiers | |
CAS Number | 201530-41-8 |
ATC code | V03AC03 (WHO) |
PubChem | CID 5493381 |
ChemSpider | 4591431 |
Chemical data | |
Formula | C21H15N3O4 |
Molar mass | 373.362 g/mol[[Script error: No such module "String".]] |
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Deferasirox (marketed as Exjade) is a rationally-designed[1] oral iron chelator. Its main use is to reduce chronic iron overload in patients who are receiving long-term blood transfusions for conditions such as beta-thalassemia and other chronic anemias.[1][2] It is the first oral medication approved in the USA for this purpose.[3]
It was approved by the United States Food and Drug Administration (FDA) in November 2005.[1][3] According to FDA (May 2007), renal failure and cytopenias have been reported in patients receiving deferasirox oral suspension tablets.
Properties of deferasirox
The half-life of deferasirox is between 8 and 16 hours allowing once a day dosing. Two molecules of deferasirox are capable of binding to 1 atom of iron which are subsequently eliminated by fecal excretion. Its low molecular weight and high lipophilicity allows the drug to be taken orally unlike desferoxamine which has to be administered by IV route (intravenous infusion). Together with deferiprone, deferasirox seems to be capable of removing iron from cells (cardiac myocytes and hepatocytes) as well as removing iron from the blood.
Synthesis
Deferasirox can be prepared from simple commercially available starting materials (salicylic acid, salicylamide and 4-hydrazinobenzoic acid) in the following two-step synthetic sequence:
The condensation of salicyloyl chloride (formed in situ from salicylic acid and thionyl chloride) with salicylamide under dehydrating reaction conditions results in formation of 2-(2-hydroxyphenyl)-1,3(4H)-benzoxazin-4-one. This intermediate is isolated and reacted with 4-hydrazinobenzoic acid in the presence of base to give 4-(3,5-bis(2-hydroxyphenyl)-1,2,4-triazol-1-yl)benzoic acid (Deferasirox)[4].
Risks
Deferasirox was the #2 drug on the list of 'Most frequent suspected drugs in reported patient deaths' compiled by the Institute for Safe Medical Practices in 2009. There were 1320 deaths reported, perhaps explained by an update to the ADE data of Novartis, and a new boxed warning about gastrointestinal haemorrhage as well as kidney and liver failure. [5]
References
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- ↑ 1.0 1.1 1.2 Choudhry VP, Naithani R (2007). "Current status of iron overload and chelation with deferasirox". Indian J Pediatr. 74 (8): 759–64. doi:10.1007/s12098-007-0134-7. PMID 17785900. Free full text
- ↑ Yang LP, Keam SJ, Keating GM (2007). "Deferasirox : a review of its use in the management of transfusional chronic iron overload". Drugs. 67 (15): 2211–30. PMID 17927285.
- ↑ 3.0 3.1 "FDA Approves First Oral Drug for Chronic Iron Overload" (Press release). United States Food and Drug Administration. November 9, 2005. http://www.fda.gov/bbs/topics/news/2005/NEW01258.html. Retrieved 2007-10-31.
- ↑ Stefan Steinhauser, Uwe Heinz, Mark Bartholomä, Thomas Weyhermüller, Hanspeter Nick, Kaspar Hegetschweiler (2004). "Complex Formation of ICL670 and Related Ligands with FeIII and FeII". European Journal of Inorganic Chemistry. 2004 (21): 4177–4192. doi:10.1002/ejic.200400363. ]
- ↑ ISMP (2010). "ISMP QuarterWatch(TM)". 15 (12). ISMP Medication Safety Alert. pp. 1–3.
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