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PHYTOSPHINGOSINE

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Catalog No. T9503Cas No. 554-62-1

Phytosphingosine is a phospholipid with anticancer properties. In cancer cells, Phytosphingosine induces cell apoptosis through activation of caspase 8 and translocation of Bax.

PHYTOSPHINGOSINE

PHYTOSPHINGOSINE

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Purity: 99.81%
Catalog No. T9503Cas No. 554-62-1
Phytosphingosine is a phospholipid with anticancer properties. In cancer cells, Phytosphingosine induces cell apoptosis through activation of caspase 8 and translocation of Bax.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
25 mg$40In StockIn Stock
50 mg$52In StockIn Stock
100 mg$73In StockIn Stock
500 mg$176-In Stock
1 mL x 10 mM (in DMSO)$29In StockIn Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:99.81%
Appearance:Solid
Color:White
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Product Introduction

PHYTOSPHINGOSINE AI Summary
PHYTOSPHINGOSINE exhibits a broad spectrum of bioactivity across various biological targets and pathogens. It inhibits the proliferation of wild type human Jurkat cells and mutant Jurkat cells (SBR1, SBR2, and SBR3) with IC50 values of 3750.0 nM, 6570.0 nM, 5290.0 nM, and 4120.0 nM, respectively, as measured by MTT assay. The resistance indices for these mutant cell lines are 1.8, 1.4, and 1.1. The compound also shows fungicidal activity against various Candida species with a minimum fungicidal concentration (MFC) of 1.0 µg/ml. It inhibits Rhodococcus sp. M777 Endoglycoceramidase 2 with a Ki value of 850000.0 nM and affects mutant variants of this enzyme. Additional bioactivities include inhibition of Bacillus subtilis Sfp phosphopantetheinyl transferase (PPTase) with a potency of 31622.8 nM, the vitamin D receptor (VDR) with a potency of 79432.8 nM, and Polymerase Kappa with a potency of 29934.9 nM. It also demonstrates partial inhibition of electric eel AChE (24.41% at 2 mg/ml) and horse BChE (7.46% at the same concentration). Notably, PHYTOSPHINGOSINE shows antiviral activity against SARS-CoV-2, inhibiting virus-induced cytotoxicity in Caco-2 and VERO-6 cells, with varying inhibition rates and IC50 values exceeding 20000.0 nM. Additionally, the compound inhibits SARS-CoV-2 3CL-Pro protease activity, although with a negative percentage inhibition at 20 µM. PHYTOSPHINGOSINE also demonstrates minor inhibition of human HDAC6 enzyme, with inhibition percentages of 0.56% and 4.33% in different enzymatic assays..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Phytosphingosine is a phospholipid with anticancer properties. In cancer cells, Phytosphingosine induces cell apoptosis through activation of caspase 8 and translocation of Bax.
Chemical Properties
Molecular Weight317.51
FormulaC18H39NO3
Cas No.554-62-1
SmilesCCCCCCCCCCCCCC[C@@H](O)[C@@H](O)[C@@H](N)CO
Relative Density.1.31g/cm3
Storage & Solubility Information
Storagekeep away from direct sunlight,store at low temperature,store under nitrogen | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 7.5 mg/mL (23.62 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 4 mg/mL (12.6 mM), Sonication is recommended.
Please add the solvents sequentially, clarifying the solution as much as possible before adding the next one. Dissolve by heating and/or sonication if necessary. Working solution is recommended to be prepared and used immediately. The formulation provided above is for reference purposes only. In vivo formulations may vary and should be modified based on specific experimental conditions.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.1495 mL15.7475 mL31.4951 mL157.4754 mL
5 mM0.6299 mL3.1495 mL6.2990 mL31.4951 mL
10 mM0.3150 mL1.5748 mL3.1495 mL15.7475 mL
20 mM0.1575 mL0.7874 mL1.5748 mL7.8738 mL

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In Vivo Formulation Calculator (Clear solution)

Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.
Stock Solution Preparation:

Dissolve 2 mg of the compound in 100 μL DMSOTargetMol | reagent 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.

Preparation of the In Vivo Formulation:

1) Add 100 μL of the DMSOTargetMol | reagent stock solution to 400 μL PEG300TargetMol | reagent 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 ddH2OTargetMol | reagent and mix thoroughly until a homogeneous solution is obtained.

This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
1 Enter information below:
mg/kg
g
μL
2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

Dose Conversion

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Tech Support

Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc

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