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Cytochrome P450 inhibitor, Itraconazole, Purity ≥98%
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Cat. No.: X24-08-YM375

Cytochrome P450 inhibitor, Itraconazole, Purity ≥98%

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Synonym: 84625-61-6; Oriconazole; Itraconazol; Itrizole; Itrizole (TN); Sporanox (TN); ITCZ; 2-Butan-2-yl-4-[4-[4-[4-[[(2R,4S)-2-(2,4-dichlorophenyl)-2-(1,2,4-triazol-1-ylmethyl)-1,3-dioxolan-4-yl]methoxy]phenyl]piperazin-1-yl]phenyl]-1,2,4-triazol-3-one

  • MDL: MFCD00941396
  • CAS Number: 84625-61-6
  • Compound CID: 55283
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Product Size
100 mg; 250 mg; 500 mg; 1000 mg
Price
Datasheet
Datasheet
MSDS
MSDS
Properties
Description
Itraconazole, soluble in warmed DMSO and insoluble in water and ethanol, is an effective cell metabolism inhibitor, that has the ability to prevent the pathway of metabolism by inhibiting cytochrome P450.
Molecular Weight
705.65
Molecular Formula
C35H38Cl2N8O4
Form
Lyophilized powder
Purity
≥98%
Titer
Free from inappropriate visible particulates, foreign matter, discoloration, or other defects
Solubility
In vitro: DMSO (warmed): 7 mg/mL (9.91 mM); Water: insoluble; Ethanol: insoluble; In vivo: 5% DMSO + 40% PEG 300 + 10% Tween 80 + 45% ddH2O, 1.66 mg/mL
Applications
Itraconazole is a metabolism inhibitor that can be studied extensively for its potential therapeutic applications in the treatment of fungal infections, including aspergillosis, blastomycosis, histoplasmosis, and onychomycosis.
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