Cytochrome P450 inhibitor, Ozagrel, Purity ≥98%

Cat. No.: X24-08-YM379

Cytochrome P450 inhibitor, Ozagrel, Purity ≥98%

Synonym: 82571-53-7; OKY 046; OKY046; Ozagrel free acid; (E)-3-[4-(Imidazol-1-ylmethyl)phenyl]prop-2-enoic acid

  • MDL: MFCD00868231
  • CAS Number: 82571-53-7
  • Compound CID: 5282440
Product Size
10 mg; 25 mg; 50 mg; 100 mg
Price
Datasheet
MSDS
Properties
Description
Ozagrel, 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. It targets the thromboxane A2 synthetase.
Molecular Weight
228.25
Molecular Formula
C13H12N2O2
Targets
Thromboxane A2 synthetase: 11 nM
Form
Lyophilized powder
Purity
≥98%
Titer
Free from inappropriate visible particulates, foreign matter, discoloration, or other defects
Solubility
In vitro: DMSO: 44 mg/mL (192.77 mM); Water: insoluble; Ethanol: insoluble
Stability
In its lyophilized form, the chemical remains stable for 36 months.
Quality Level
Research grade
Applications
Ozagrel is a metabolism inhibitor that can be used for its ability to reduce blood clotting and improve blood flow by inhibiting the production of thromboxane A2, a compound that promotes platelet aggregation and vasoconstriction.
Storage
Store at -20ºC, and keep desiccated.
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