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CPX-351

(Synonyms: Vyxeos, CPX351, CPX 351) Copy Product Info
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Synonyms: Vyxeos, CPX351, CPX 351

Catalog No. T31088 Copy Product Info
Purity: 99.76%
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CPX-351 (Vyxeos) is a liposomal formulation of cytarabine and daunorubicin with potential antitumor activity. CPX-351 delivers these two compounds to leukemia cells in a synergistic 5:1 ratio, with higher delivery rates than in normal bone marrow cells. CPX-351 is indicated for the treatment of acute myeloid leukemia.
CPX-351
Cas No. 1256639-86-7
Pack SizePriceUSA StockGlobal StockQuantity
1 mg$1,270In StockIn Stock
5 mg$2,550-In Stock
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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For research use only—not for human use. No sales to individuals. Use as intended only.
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Purity:99.76%
Appearance:Solid
Color:Red
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Product Introduction

Bioactivity
Description
CPX-351 (Vyxeos) is a liposomal formulation of cytarabine and daunorubicin with potential antitumor activity. CPX-351 delivers these two compounds to leukemia cells in a synergistic 5:1 ratio, with higher delivery rates than in normal bone marrow cells. CPX-351 is indicated for the treatment of acute myeloid leukemia.
Targets & IC50
NMUR1:45 nM (Kb), NMUR1:7.35 (pA2), Primary AML cells、leukemia blast cells:0.223 µM, Cyt:Daun:0.03:0.006 uM to 10:2 uM
In vitro
Methods: p53 wild-type AML cells (MOLM-13, MV4-11, MOLM-14) were treated with CPX-351 (62.5 nM) alone or in combination with M3814 (500 nM), and apoptosis rates were assessed at various time points using Annexin V flow cytometry.
Results: M3814 significantly enhanced CPX-351-induced apoptosis in p53 wild-type AML cells, with a time-dependent increase. [2]
Methods: MOLM-13 cells were co-cultured with healthy bone marrow-derived MSCs and treated with CPX-351 alone or in combination with M3814; apoptosis was assessed by Annexin V flow cytometry.
Results: MSCs attenuated the apoptosis-inducing effect of CPX-351 monotherapy, whereas the combination of M3814 and CPX-351 significantly reversed the protective effect of MSCs and restored cytotoxicity against AML cells.[2]
In vivo
Methods: C57BL/6 mice (female, 8–10 weeks old) received tail vein injections (CPX-351 group: 12:5.3 mg/kg; “7+3” group: 600:9 mg/kg) every 3 days for a total of 3 doses.
Results: The “7+3” group exhibited intestinal injury, colon shortening, inflammatory infiltration, increased permeability, and bacterial translocation. The CPX-351 group showed no such pathological changes, maintaining intestinal barrier integrity and immune function. [1]
SynonymsVyxeos, CPX351, CPX 351
Chemical Properties
Molecular Weight770.74
FormulaC36H42N4O15
Cas No.1256639-86-7
SmilesO[C@@H]1[C@@H](O[C@H](CO)[C@H]1O)N2C(=O)N=C(N)C=C2.OC=1C2=C([C@@H](O[C@H]3C[C@H](N)[C@H](O)[C@H](C)O3)C[C@@](C(C)=O)(O)C2)C(O)=C4C1C(=O)C=5C(C4=O)=C(OC)C=CC5
Relative Density.1.31g/cm3
Storage & Solubility Information
StorageKeep away from moisture,Store at low temperature Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature.

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TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.
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Preparation of the In Vivo Formulation:

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Keywords

Related Tags: CPX-351 chemical structure | CPX-351 in vivo | CPX-351 in vitro | CPX-351 formula | CPX-351 molecular weight