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Synonyms: Vyxeos, CPX351, CPX 351

| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 1 mg | $1,270 | In Stock | In Stock | |
| 5 mg | $2,550 | - | In Stock |
| 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] |
| Synonyms | Vyxeos, CPX351, CPX 351 |
| Molecular Weight | 770.74 |
| Formula | C36H42N4O15 |
| Cas No. | 1256639-86-7 |
| Smiles | O[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 | Keep 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. |
Dissolve 2 mg of the compound in 100 μL DMSO
to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.
1) Add 100 μL of the DMSO
stock solution to 400 μL PEG300
and mix thoroughly until the solution becomes clear.
2) Add 50 μL Tween 80 and mix well until fully clarified.
3) Add 450 μL Saline,PBS or ddH2O
and mix thoroughly until a homogeneous solution is obtained.
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