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Vinflunine ditartrate, a fluorinated microtubule inhibitor and member of the Vinca alkaloids family, exhibits anti-angiogenic, vascular-disrupting, and anti-metastatic properties. It presents a potential avenue for studying transitional cell carcinoma of the urothelial tract, non-small cell lung cancer, and breast carcinoma[1][2].

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 5 mg | $1,088 | Inquiry | Inquiry | |
| 10 mg | $1,744 | Inquiry | Inquiry |
| Description | Vinflunine ditartrate, a fluorinated microtubule inhibitor and member of the Vinca alkaloids family, exhibits anti-angiogenic, vascular-disrupting, and anti-metastatic properties. It presents a potential avenue for studying transitional cell carcinoma of the urothelial tract, non-small cell lung cancer, and breast carcinoma[1][2]. |
| In vitro | Vinflunine (0.01-10 μM; 45 min) rapidly alters endothelial cell morphology, causing retraction and rounding[2]. Within 1 hour at the same concentrations, it disrupts capillary-like structure formation and inhibits motility, with an IC50 of 0.71 μM[2]. Over 1 to 72 hours, Vinflunine (0.001-10 μM) effectively suppresses endothelial cell proliferation in vitro[2]. |
| In vivo | Vinflunine (0.08-20 mg/kg; i.v.) reduces the number of experimental liver metastases by human LS174T colon cancer cells. Vinflunine (0.63-5 mg/kg; i.v. before and 2 days after Matrigel implantation) inhibits the bFGF-induced angiogenic response in mice in a dose-dependent manner. [Animal Model: Female athymic nude mice (BALB/c/Ola/Hsd-nu) implanted with LS174T cells][2]. |
| Molecular Weight | 967.03 |
| Formula | C49H60F2N4O14 |
| Cas No. | 194468-36-5 |
| Smiles | O[C@H]([C@@H](O)C(O)=O)C(O)=O.[H][C@@]12N3CC[C@@]11c4cc(c(OC)cc4N(C)[C@@]1([H])[C@](O)([C@H](OC(C)=O)[C@]2(CC)C=CC3)C(=O)OC)[C@]1(C[C@]2([H])C[C@H](C[N@@](C2)Cc2c1[nH]c1ccccc21)C(C)(F)F)C(=O)OC |c:41| |
| Storage | 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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