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5A2-SC8

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Catalog No. T74450Cas No. 1857341-90-2

5A2-SC8 is an ionizable cationic lipid that is an ideal vehicle for the delivery of small RNAs, interacts with negatively charged cell membranes, and can be used for gene delivery and drug delivery.

5A2-SC8

5A2-SC8

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Catalog No. T74450Cas No. 1857341-90-2
5A2-SC8 is an ionizable cationic lipid that is an ideal vehicle for the delivery of small RNAs, interacts with negatively charged cell membranes, and can be used for gene delivery and drug delivery.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$239In StockIn Stock
5 mg$591In StockIn Stock
10 mg$987In StockIn Stock
25 mg$1,980In StockIn Stock
1 mL x 10 mM (in DMSO)$1,630-In Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
This molecule is a custom-made product. TargetMol has an excellent synthesis team with the experience and capability to provide you with cost-effective products.If you have any questions, please feel free to contact us. We are committed to serving you wholeheartedly.
All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.
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Purity:≥98%
Color:Transparent
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Product Introduction

Bioactivity
Description
5A2-SC8 is an ionizable cationic lipid that is an ideal vehicle for the delivery of small RNAs, interacts with negatively charged cell membranes, and can be used for gene delivery and drug delivery.
In vitro
5A2-SC8 is taken up by hepatocytes by binding to the LDL receptor (LDL-R) on the surface of hepatocytes and undergoing receptor-mediated endocytosis with the aid of a crown of surface-adsorbed ApoE protein. [2]
In vivo
A single dose of 75 mg/kg 5A2-SC8 administered intravenously was well tolerated in chronically ill mice with invasive hepatocellular carcinoma and did not adversely affect survival. [1]
Intravenous injection of 0.5 mg/kg 5A2-SC8 was effective in crossing the first barrier of hepatic Kupffer cells and was internalized by hepatocytes after 6 hours in the presence of siFVII labeled with Cy5.5 dye. [2]
Chemical Properties
Molecular Weight1841.71
FormulaC93H173N5O20S5
Cas No.1857341-90-2
SmilesO=C(OCCOC(=O)C(C)CSCCCCCCCC)CCN(CCNCCN(CCC(=O)OCCOC(=O)C(C)CSCCCCCCCC)CCC(=O)OCCOC(=O)C(C)CSCCCCCCCC)CCNCCN(CCC(=O)OCCOC(=O)C(C)CSCCCCCCCC)CCC(=O)OCCOC(=O)C(C)CSCCCCCCCC
Storage & Solubility Information
Storagekeep away from moisture | Pure form: -20°C for 3 years | In solvent: -80°C for 1 year
Solubility Information
DMSO: 80 mg/mL (43.44 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM0.5430 mL2.7149 mL5.4297 mL27.1487 mL
5 mM0.1086 mL0.5430 mL1.0859 mL5.4297 mL
10 mM0.0543 mL0.2715 mL0.5430 mL2.7149 mL
20 mM0.0271 mL0.1357 mL0.2715 mL1.3574 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
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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

Keywords

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