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Sardomozide (Synonyms: SAM-486A, CGP 48664)

Catalog No. T12833 Copy Product Info
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Sardomozide is an inhibitor of S-adenosylmethionine decarboxylase (SAMDC)(IC50 of 5 nM).

Sardomozide

Copy Product Info
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Catalog No. T12833
Synonyms SAM-486A, CGP 48664

Sardomozide is an inhibitor of S-adenosylmethionine decarboxylase (SAMDC)(IC50 of 5 nM).

Sardomozide
Cas No. 149400-88-4
Pack SizePriceUSA StockGlobal StockQuantity
25 mg$1,5201-2 weeks1-2 weeks
50 mg$1,9801-2 weeks1-2 weeks
100 mg$2,5001-2 weeks1-2 weeks
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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Custom-made molecule. TargetMol’s expert synthesis team delivers cost-effective solutions. Contact us for inquiries. Committed to serving you.However, due to objective factors, there is a small probability that the synthesis may not be successful during the R&D process. We appreciate your understanding.
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Product Introduction

Bioactivity
Description
Sardomozide is an inhibitor of S-adenosylmethionine decarboxylase (SAMDC)(IC50 of 5 nM).
Targets&IC50
SAMDC:5 nM
In vitro
Sardomozide acts as an inhibitor of S-adenosylmethionine decarboxylase (SAMDC), showing potency with an IC50 value of 5 nM in cell assays. With a 48-hour exposure to 3 μM of Sardomozide, the activity of intracellular SAMDC is diminished to 10% compared to the control[1]. Additionally, in cells grown in the presence of Sardomozide, specifically CHO/664 cells treated with DENSPM, there is an absence of vacuole formation. These cells also exhibit inhibited growth and maintain DENSPM levels comparable to those in parental CHO cells[2].
SynonymsSAM-486A, CGP 48664
Chemical Properties
Molecular Weight230.27
FormulaC11H14N6
Cas No.149400-88-4
SmilesC(=N)(N)C1=C2C(C(=NNC(=N)N)CC2)=CC=C1
Relative Density.1.54 g/cm3 (Predicted)
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.

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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:
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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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