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Ilmofosine (BM41440) is a potent and selective inhibitor of protein kinase C (protein kinase C). It induces cell cycle arrest in the G2 phase and also acts as an antileishmanial agent.

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 10 mg | Inquiry | 10-14 weeks | 10-14 weeks | |
| 50 mg | Inquiry | 10-14 weeks | 10-14 weeks |
| Description | Ilmofosine (BM41440) is a potent and selective inhibitor of protein kinase C (protein kinase C). It induces cell cycle arrest in the G2 phase and also acts as an antileishmanial agent. |
| In vitro | Ilmofosine inhibits the promastigotes and antimony-resistant strains of Leishmania, with an ED₅₀ of 3.73 µM and 3.46 µM, respectively. Additionally, Ilmofosine at a concentration of 15 µM for 48 hours induces cell cycle arrest in CA46 cells at the G2 phase. |
| Synonyms | BM41440 |
| Molecular Weight | 525.77 |
| Formula | C26H56NO5PS |
| Cas No. | 83519-04-4 |
| Smiles | O=P([O-])(OCC[N+](C)(C)C)OCC(COC)CSCCCCCCCCCCCCCCCC |
| 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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