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Cytochrome P450 inhibitor, Deferasirox, Purity ≥98%
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Cat. No.: X24-08-YM374

Cytochrome P450 inhibitor, Deferasirox, Purity ≥98%

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Synonym: 201530-41-8; ICL-670; ICL-670A; CGP-72670; 4-[3,5-Bis(2-hydroxyphenyl)-1,2,4-triazol-1-yl]benzoic acid

  • MDL: MFCD09751362
  • CAS Number: 201530-41-8
  • Compound CID: 214348
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Product Size
5 mg; 10 mg; 25 mg; 50 mg
Price
Datasheet
Datasheet
MSDS
MSDS
Properties
Description
Deferasirox, soluble in DMSO and ethanol and insoluble in water, is an effective cell metabolism inhibitor, that has the ability to prevent the pathway of metabolism by inhibiting cytochrome P450.
Molecular Weight
373.36
Molecular Formula
C21H15N3O4
Form
Lyophilized powder
Purity
≥98%
Titer
Free from inappropriate visible particulates, foreign matter, discoloration, or other defects
Solubility
In vitro: DMSO: 64 mg/mL (171.42 mM); Water: insoluble; Ethanol: 2 mg/mL; In vivo: 5% DMSO + 40% PEG 300 + 5% Tween 80 + 50% H2O, 3.5 mg/mL
Applications
Deferasirox is a metabolism inhibitor that can be studied extensively for its potential therapeutic applications in the treatment of chronic iron overload due to conditions such as thalassemia or sideroblastic anemia, often resulting from repeated blood transfusions.
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