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Oral iron chelator

Deferasirox

Deferasirox
All data from the card 29
Pronunciation
de FER a sir ox
Trade names
Exjade, others
Other names
CGP-72670, ICL-670A, IC L670
AHFS/Drugs.com
Monograph
MedlinePlus
a606002
License data
US DailyMed: Deferasirox
Pregnancycategory
AU: C
Routes ofadministration
By mouth
ATC code
V03AC03 (WHO)
Legal status
AU: S4 (Prescription only) UK: POM (Prescription only) US: ℞-only EU: Rx-only In general: ℞ (Prescription only)
Bioavailability
70%
Protein binding
99%
Metabolism
Liver glucuronidation
Elimination half-life
8 to 16 hours
Excretion
Fecal (84%) and kidney (8%)
CAS Number
201530-41-8
PubChem CID
214348
DrugBank
DB01609
ChemSpider
4591431
UNII
V8G4MOF2V9
KEGG
D03669
ChEBI
CHEBI:49005
ChEMBL
ChEMBL550348
CompTox Dashboard (EPA)
DTXSID1048596
ECHA InfoCard
100.211.077
Formula
C21H15N3O4
Molar mass
373.368 g·mol−1
3D model (JSmol)
Interactive image
Density
1.4±0.1 g/cm3

Deferasirox, sold under the brand name Exjade among others, is an 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. It is the first oral medication approved in the United States for this purpose.

It was approved by the US Food and Drug Administration (FDA) in November 2005. According to the FDA (May 2007), kidney failure and cytopenias have been reported in patients receiving deferasirox tablets for oral suspension. It is approved in the European Union by the European Medicines Agency (EMA) for children six years and older for chronic iron overload from repeated blood transfusions. It is on the World Health Organization's List of Essential Medicines.

In July 2020, Teva decided to discontinue deferasirox. It is available as a generic medication.

Properties

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 deferoxamine 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

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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).

Risks

Deferasirox ranked second on the list of drugs most frequently suspected in reported patient deaths compiled for 2019, by the Institute for Safe Medical Practices, with 1320 suspected deaths. A boxed warning was added in the same year with regard to kidney failure, liver failure and gastrointestinal bleeding. It is suspected that the main driver of this spike in suspected deaths relates to the re-analysis of adverse event data by Novartis.

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Text from Wikipedia, CC BY-SA 4.0 · Source article