Miltefosine

目录号: A14138

PI3K/Akt inhibitor

Miltefosine

Miltefosine Chemical Structure

CAS NO. 58066-85-6

Miltefosine inhibits PI3K/Akt activity with ED50 of 17.2 μM and 8.1 μM in carcinoma cell lines A431 and HeLa

库存: 现货

规格 价格 数量
100 mg
¥ 650.00
500 mg
¥ 1,900.00
10mM * 1mL in DMSO
¥ 640.00
Warning 产品仅用于科学研究,不针对患者销售,望谅解.

详情

Miltefosine inhibits PI3K/Akt activity with ED50 of 17.2 μM and 8.1 μM in carcinoma cell lines A431 and HeLa
Targets
Akt PI3K PKC
N/A~7 μM
In vitro (25°C) DMSO 82 mg/mL (201.19 mM)
Water <1 mg/mL (<1 mM)
Ethanol 82 mg/mL (201.19 mM)
In vivo Saline 30 mg/mL
* <1 mg/ml means slightly soluble or insoluble.
* Please note that Adooq tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations.
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
0.1 mM 24.53 mL 122.67 mL 245.34 mL
0.5 mM 4.91 mL 24.53 mL 49.07 mL
1 mM 2.45 mL 12.27 mL 24.53 mL
5 mM 0.49 mL 2.45 mL 4.91 mL

*The above data is based on the productmolecular weight 407.6. Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.

Technical Details

目录号 A14138
MECHANISM OF ACTION Inhibitor
M. Wt 407.6
Formula C21H46NO4P
Solubility DMSO
Purity >98%
Storage at -20°C 3 years Powder
CAS No. 58066-85-6
Synonyms HePC
SMILES CCCCCCCCCCCCCCCCOP(=O)([O-])OCC[N+](C)(C)C

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