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Deferasirox

Cat. No. M5557
Deferasirox Structure
Synonym:

CGP-72670, ICL-670

Size Price Availability Quantity
2mg USD 30  USD30 In stock
5mg USD 50  USD50 In stock
10mg USD 70  USD70 In stock
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Quality Control & Documentation
Biological Activity

Deferasirox (ICL-670) is an iron chelator that causes iron loss that promotes BclxL downregulation and cell death. Deferasirox (ICL-670) also induced P450 3A4 and inhibited 2C8 and 1A2.

Chemical Information
Molecular Weight 373.36
Formula C21H15N3O4
CAS Number 201530-41-8
Solubility (25°C) DMSO 90 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
Conversion of different model animals based on BSA (PMID: 27057123)
Species Mouse Rat Rabbit Guinea pig Hamster Dog
Weight (kg) 0.02 0.15 1.8 0.4 0.08 10
Body Surface Area (m2) 0.007 0.025 0.15 0.05 0.02 0.5
Km factor 3 6 12 8 5 20
Animal A (mg/kg) = Animal B (mg/kg) multiplied by  Animal B Km
Animal A Km

For example, to modify the dose of Compound A used for a mouse (20 mg/kg) to a dose based on the BSA for a rat, multiply 20 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for Compound A of 10 mg/kg.

References

[1] Chang HH, et al. Ann Hematol. The long-term efficacy and tolerability of oral deferasirox for patients with transfusion-dependent β-thalassemia in Taiwan.

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Keywords: Deferasirox, CGP-72670, ICL-670 supplier, Cytochrome P450 (e.g. CYP17), inhibitors, activators


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