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Miltefosine

Catalog No. T0033   CAS 58066-85-6
Synonyms: HePC, Hexadecyl phosphocholine

Miltefosine (HePC) is the treatment of visceral and cutaneous leishmaniasis drug , and is proceeding clinical trials for this in several countries. Several medical agents produce some potency against visceral or cutaneous leishmaniasis, however a 2005 survey concluded that miltefosine is the only effective oral treatment for both forms of leishmaniasis.

All products from TargetMol are for Research Use Only. Not for Human or Veterinary or Therapeutic Use.
Miltefosine Chemical Structure
Miltefosine, CAS 58066-85-6
Pack Size Availability Price/USD Quantity
50 mg In stock $ 47.00
100 mg In stock $ 56.00
200 mg In stock $ 85.00
500 mg In stock $ 117.00
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Purity: 99.51%
Purity: 98%
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Biological Description
Chemical Properties
Storage & Solubility Information
Description Miltefosine (HePC) is the treatment of visceral and cutaneous leishmaniasis drug , and is proceeding clinical trials for this in several countries. Several medical agents produce some potency against visceral or cutaneous leishmaniasis, however a 2005 survey concluded that miltefosine is the only effective oral treatment for both forms of leishmaniasis.
Targets&IC50 PKC:7 μM
Kinase Assay Levels of enzymatically active caspase-3 are quantified using the ApoAlert Caspase Fluorescent assay kit. Briefly, 1×106 BC-1 PEL cells are treated with 50 μM Miltefosine, 50 μM Perifosine, or 20 nM NVP-BEZ235, as well as the respective vehicle controls. Cells are harvested and lysed 12 hours later. Equivalent micrograms of cell lysate for all samples are incubated with a fluorogenic caspase-3 substrate (DEVD-AFC). Cleavage of DEVD by caspase-3 releases AFC, the fluorescence of which is measured using a FLUOstar OPTIMA fluorometer, with excitation and emission filter wavelengths set to 400 and 505 nm, respectively[3].
Cell Research 2 &times 105 PEL cells are treated with the therapeutic compounds at the indicated doses or with appropriate vehicle as a negative control. Cells are followed for 96 hours, and cell viability is determined by trypan blue exclusion performed in quadruplicate. (Only for Reference)
Synonyms HePC, Hexadecyl phosphocholine
Molecular Weight 407.57
Formula C21H46NO4P
CAS No. 58066-85-6

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

H2O: 10 mM

DMSO: Insoluble

TargetMolReferences and Literature

1. Uberall F, et al. Y Res, 1991, 51(3), 807-812. 2. Chugh P, et al. Retrovirology, 2008, 5, 11. 3. Ruiter GA, et al. Anticancer Drugs, 2003, 14(2), 167-173.

Related compound libraries

This product is contained In the following compound libraries:
Drug Repurposing Compound Library Inhibitor Library Kinase Inhibitor Library Anti-Cancer Clinical Compound Library FDA-Approved Kinase Inhibitor Library Anti-Cancer Approved Drug Library Anti-Cancer Drug Library Anti-Lung Cancer Compound Library Approved Drug Library Neuronal Differentiation Compound Library

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Keywords

Miltefosine 58066-85-6 Chromatin/Epigenetic Cytoskeletal Signaling Microbiology/Virology PI3K/Akt/mTOR signaling Proteases/Proteasome Akt HIV Protease PKC HePC PKB inhibit HIV Inhibitor Protein kinase B Hexadecyl phosphocholine Human immunodeficiency virus inhibitor

 

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