Pegcetacoplan (acetate)
Referentie HY-P3252A-1mg
Formaat : 1mg
Merk : MedChemExpress
| Description |
Pegcetacoplan acetate is a pegylated complement C3/C3b inhibitor. Pegcetacoplan acetate acts by specifically binding to and inhibiting C3 and C3b, thereby suppressing the complement cascade at its proximal stage. Pegcetacoplan is not a known inhibitor or inducer of CYP450 isoenzymes. Pegcetacoplan acetate can be used for the research of complement-mediated diseases, including paroxysmal nocturnal hemoglobinuria (PNH) and age-related macular degeneration (AMD)[1][2][3][4]. |
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| In Vitro |
Pegcetacoplan acetate targets C3 in the complement cascade, upstream of C5, thereby providing control over both intravascular and extravascular haemolysis[3]. MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only. |
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| Essai clinique |
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| Formule |
(C2H4O)nC170H248N50O47S4.xC2H4O2 |
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| Appearance |
Solid |
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| Color |
White to off-white |
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| Livraison | Room temperature in continental US; may vary elsewhere. |
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| Stockage |
Sealed storage, away from moisture
*In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture) |
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| Solvant et solubilité |
In Vitro:
DMSO : 50 mg/mL (Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO) 3 M Sodium Acetate Solution (pH 5.2) : ≥ 12.5 mg/mL *"≥" means soluble, but saturation unknown. Select the appropriate dissolution method based on your experimental animal and administration route.
For the following dissolution methods, please ensure to first prepare a clear stock solution using an In Vitro approach and then sequentially add co-solvents:
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| Pureté et documentation | |||||||
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