Description：

Miltefosine inhibits PI3K/Akt activity with ED50 of 17.2 μM and 8.1 μM in carcinoma cell lines A431 and HeLa, first oral drug for Visceral leishmaniasis, effective against both promastigotes and amastigotes.

Chemical Information：

Molecular Weight (MW)		407.57
Formula		C21H46NO4P
CAS No.		58066-85-6
Solubility (25°C) *	DMSO	Insoluble
	Water	81 mg/mL (198.73 mM)
	Alcohol	81 mg/mL (198.73 mM)

Preparing Stock Solutions

Concentration Volume (DMSO) Mass	1 mg	5 mg	10 mg
1 mM	2.4536 mL	12.2678 mL	24.5357 mL
5 mM	0.4907 mL	2.4536 mL	4.9071 mL
10 mM	0.2454 mL	1.2268 mL	2.4536 mL
50 mM	0.0491 mL	0.2454 mL	0.4907 mL

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