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Sandoz 58-035

(Synonyms: Sandoz58-035) Copy Product Info
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Synonyms: Sandoz58-035

Catalog No. T88328 Copy Product Info
Purity: 99.83%
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Sandoz 58-035 acts as a competitive inhibitor of cholesterol acyltransferase (ACAT), significantly blocking (>98%) the hormonally stimulated esterification of cholesterol within cells. Sandoz 58-035 is therefore used in lipid metabolism and enzymology research systems to investigate ACAT-dependent cholesterol esterification processes, intracellular cholesterol trafficking, and regulation of sterol storage pathways in cellular models of lipid homeostasis.
Sandoz 58-035
Cas No. 78934-83-5
Pack SizePriceUSA StockGlobal StockQuantity
1 mg$89-In Stock
5 mg$189-In Stock
10 mg$313-In Stock
25 mgPreferential-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:99.83%
Appearance:Solid
Color:White
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Product Introduction

Bioactivity
Description
Sandoz 58-035 acts as a competitive inhibitor of cholesterol acyltransferase (ACAT), significantly blocking (>98%) the hormonally stimulated esterification of cholesterol within cells. Sandoz 58-035 is therefore used in lipid metabolism and enzymology research systems to investigate ACAT-dependent cholesterol esterification processes, intracellular cholesterol trafficking, and regulation of sterol storage pathways in cellular models of lipid homeostasis.
In vivo
Method: Granulosa cells were cultured under limited or no serum conditions and treated long-term (2–6 days) with ACAT inhibitor Sandoz 58-035. Progesterone production was measured under basal conditions and after stimulation with estradiol, FSH, estradiol+FSH, or insulin. LDL was used as exogenous cholesterol. Acute (2–20 h) effects were also tested in swine and hamster ovarian cells.
Result: Long-term treatment with Sandoz 58-035 significantly increased basal progesterone production and amplified hormone-stimulated progesterone production by 2–10 fold. The effect was mimicked by LDL, and co-treatment with LDL and Sandoz 58-035 did not further increase steroidogenesis. Acute (2–20 h) treatment did not alter progesterone biosynthesis in swine or hamster ovarian cells.
SynonymsSandoz58-035
Chemical Properties
Molecular Weight465.79
FormulaC30H47NOSi
Cas No.78934-83-5
SmilesO=C(NC(C=1C=CC=CC1)CC2=CC=C(C=C2)C)CC[Si](C)(C)CCCCCCCCCC
Storage & Solubility Information
StorageKeep away from direct sunlight,Keep 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: 80 mg/mL (171.75 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.1469 mL10.7345 mL21.4689 mL107.3445 mL
5 mM0.4294 mL2.1469 mL4.2938 mL21.4689 mL
10 mM0.2147 mL1.0734 mL2.1469 mL10.7345 mL
20 mM0.1073 mL0.5367 mL1.0734 mL5.3672 mL
50 mM0.0429 mL0.2147 mL0.4294 mL2.1469 mL
100 mM0.0215 mL0.1073 mL0.2147 mL1.0734 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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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

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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: Sandoz 58-035 chemical structure | Sandoz 58-035 in vivo | Sandoz 58-035 formula | Sandoz 58-035 molecular weight