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  3. Ilmofosine

Ilmofosine (BM41440) is a potent and selective protein kinase C inhibitor. Ilmofosine induces cell cycle arrest at the G2 phase. Ilmofosine also is an anti-leishmanial agent.

For research use only. We do not sell to patients.

Ilmofosine Chemical Structure

Ilmofosine Chemical Structure

CAS No. : 83519-04-4

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Description

Ilmofosine (BM41440) is a potent and selective protein kinase C inhibitor. Ilmofosine induces cell cycle arrest at the G2 phase. Ilmofosine also is an anti-leishmanial agent[1][2].

In Vitro

Ilmofosine inhibits amastigotes of Leishmania donovani and an antimony-resistant line of L. infantum with ED50 values of 3.73, 3.46 µM[1].
Ilmofosine (15 µM; 48 h) induces cell cycle arrest at G2 phase in CA46 cells[2].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Cycle Analysis[2]

Cell Line: CA46 cells
Concentration: 15 µM
Incubation Time: 48 h
Result: Induced cell cycle arrest at G2-phase.
Molecular Weight

525.77

Formula

C26H56NO5PS

CAS No.
SMILES

CCCCCCCCCCCCCCCCSCC(COC)COP(OCC[N+](C)(C)C)([O-])=O

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Room temperature in continental US; may vary elsewhere.

Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

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Ilmofosine Related Classifications

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  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Ilmofosine
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HY-133838
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