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Cytochrome P450 inhibitor, Posaconazole, Purity ≥98%
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Cat. No.: X24-08-YM380

Cytochrome P450 inhibitor, Posaconazole, Purity ≥98%

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Synonym: 171228-49-2; Noxafil; Posaconazole SP; SCH56592; Schering 56592; 4-[4-[4-[4-[[(3R,5R)-5-(2,4-Difluorophenyl)-5-(1,2,4-triazol-1-ylmethyl)oxolan-3-yl]methoxy]phenyl]piperazin-1-yl]phenyl]-2-[(2S,3S)-2-hydroxypentan-3-yl]-1,2,4-triazol-3-one

  • MDL: MFCD00941162
  • CAS Number: 171228-49-2
  • Compound CID: 468595
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Product Size
5 mg; 10 mg; 25 mg; 50 mg
Price
Datasheet
Datasheet
MSDS
MSDS
Properties
Description
Posaconazole, soluble in 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
700.8
Molecular Formula
C37H42F2N8O4
Form
Lyophilized powder
Purity
≥98%
Titer
Free from inappropriate visible particulates, foreign matter, discoloration, or other defects
Solubility
In vitro: DMSO: 90 mg/mL (128.42 mM); Water: insoluble; Ethanol: insoluble; In vivo: 1% DMSO + 30% polyethylene glycol + 1% Tween 80, 28 mg/mL
Applications
Posaconazole is a metabolism inhibitor that can be studied extensively for its potential therapeutic applications in the treatment of a variety of fungal infections.
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