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Pactimibe sulfate

(Synonyms: CS-505, CS 505) Copy Product Info
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Synonyms: CS-505, CS 505

Catalog No. T62974 Copy Product Info
Purity: 99.08%
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Pactimibe sulfate (CS-505) is a dual ACAT1/2 inhibitor that targets ACAT1 with an IC50 value of 4.9 μM and ACAT2 with an IC50 value of 3.0 μM. Pactimibe sulfate (CS-505) inhibits oleoyl-CoA noncompetitively with a Ki value of 5.6 μM and significantly suppresses cholesterol ester formation with an IC50 value of 6.7 μM. Pactimibe sulfate (CS-505) reduces plasma cholesterol activity and demonstrates anti-atherogenic potential. Pactimibe sulfate (CS-505) is applicable to lipid metabolism, atherosclerosis, and cholesterol homeostasis-related research.
Pactimibe sulfate
Cas No. 608510-47-0
Pack SizePriceUSA StockGlobal StockQuantity
1 mg$133-In Stock
5 mg$333-In Stock
10 mg$596-In Stock
25 mg$1,230-In Stock
50 mg$1,880-In Stock
1 mL x 10 mM (in DMSO)$342-In Stock
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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For research use only—not for human use. No sales to individuals. Use as intended only.
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Purity:99.08%
Appearance:Solid
Color:Purple
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Product Introduction

Bioactivity
Description
Pactimibe sulfate (CS-505) is a dual ACAT1/2 inhibitor that targets ACAT1 with an IC50 value of 4.9 μM and ACAT2 with an IC50 value of 3.0 μM. Pactimibe sulfate (CS-505) inhibits oleoyl-CoA noncompetitively with a Ki value of 5.6 μM and significantly suppresses cholesterol ester formation with an IC50 value of 6.7 μM. Pactimibe sulfate (CS-505) reduces plasma cholesterol activity and demonstrates anti-atherogenic potential. Pactimibe sulfate (CS-505) is applicable to lipid metabolism, atherosclerosis, and cholesterol homeostasis-related research.
Targets & IC50
ACAT2:3.0 μM, ACAT1:4.9 μM, ACAT:4.7 μM (in THP-1 cells), cholesteryl ester formation:6.7 μM, ACAT:2.7 μM (in macrophages), ACAT:2 μM (in the liver), oleoyl-CoA:5.6 μM (Ki)
In vitro
Pactimibe sulfate (CS-505) inhibits ACAT activities in the liver, macrophages and THP-1 cells with IC50 values of 2 μM, 2.7 μM and 4.7 μM, respectively[1].
Pactimibe sulfate (CS-505) inhibits ACAT1 and ACAT2 activities with IC50 values of 4.9 μM and 3 μM[1].
In vivo
Pactimibe sulfate (CS-505) (diet supplemented with 0.03 or 0.1% (w/w); 12-24weeks) significantly increases plasma triglyceride (TG) and reduces non-high density lipoprotein cholesterol (non-HDL-C) in Male apoE−/− mice[1].
Pactimibe sulfate (CS-505) (diet supplemented with 0.03 or 0.1% (w/w); 12-24weeks) reduces MMP-2 expression by 44 and 70% in Male apoE−/− mice[1].
SynonymsCS-505, CS 505
Chemical Properties
Molecular Weight931.27
FormulaC50H82N4O10S
Cas No.608510-47-0
SmilesO=C(CC1=C(C)C(CCN2CCCCCCCC)=C2C(NC(C(C)(C)C)=O)=C1C)O.O=S(O)(O)=O.O=C(CC3=C(C)C(CCN4CCCCCCCC)=C4C(NC(C(C)(C)C)=O)=C3C)O
Storage & Solubility Information
StorageKeep away from moisture, Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 96 mg/mL (103.09 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.0738 mL5.3690 mL10.7380 mL53.6901 mL
5 mM0.2148 mL1.0738 mL2.1476 mL10.7380 mL
10 mM0.1074 mL0.5369 mL1.0738 mL5.3690 mL
20 mM0.0537 mL0.2685 mL0.5369 mL2.6845 mL
50 mM0.0215 mL0.1074 mL0.2148 mL1.0738 mL
100 mM0.0107 mL0.0537 mL0.1074 mL0.5369 mL
Note : The dilution table applies only to solid products. For liquid products, please calculate the stock solution based on the stated concentration and/or density.

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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
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2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

Dose Conversion

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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
Related Tags: Pactimibe sulfate chemical structure | Pactimibe sulfate in vivo | Pactimibe sulfate in vitro | Pactimibe sulfate formula | Pactimibe sulfate molecular weight