Shopping Cart
Remove All
  • TargetMol
    Your shopping cart is currently empty

L-BUTHIONINE-(S,R)-SULFOXIMINE

Copy Product Info
🥰Excellent
Catalog No. T5371Cas No. 83730-53-4
Alias L-Butionine sulfoximine

L-Buthionine-(S,R)-sulfoximine, a cell-permeable and irreversible inhibitor of γ-glutamylcysteine synthetase (Ki <100 μM), induces oxidative stress in cells by depleting GSH.

L-BUTHIONINE-(S,R)-SULFOXIMINE

L-BUTHIONINE-(S,R)-SULFOXIMINE

Copy Product Info
🥰Excellent
Purity: 99.92%
Catalog No. T5371Alias L-Butionine sulfoximineCas No. 83730-53-4
L-Buthionine-(S,R)-sulfoximine, a cell-permeable and irreversible inhibitor of γ-glutamylcysteine synthetase (Ki <100 μM), induces oxidative stress in cells by depleting GSH.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
25 mg$33In StockIn Stock
50 mg$47In StockIn Stock
100 mg$80In StockIn Stock
Add to Cart
Add to Quotation
In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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.
Questions
TargetMol
View More

Batch Information

Select Batch
Purity:99.92%
Appearance:Solid
Color:White to Yellow
Contact us for more batch information

Resource Download

Product Introduction

Bioactivity
Description
L-Buthionine-(S,R)-sulfoximine, a cell-permeable and irreversible inhibitor of γ-glutamylcysteine synthetase (Ki <100 μM), induces oxidative stress in cells by depleting GSH.
Targets&IC50
Ovarian tumor:29 μM, Breast:8.6 μM, Melanoma:1.9 μM
In vitro
IC50 values (microM) for L-buthionine-S,R-sulfoximine (BSO) on melanoma, breast and ovarian tumor specimens were 1.9, 8.6, and 29, respectively. The IC90 for melanoma was 25.5 microM, a level 20-fold lower than steady-state levels achieved clinically [1]. GSH loss induced by L-buthionine-S,R-sulfoximine (BSO) leads to overproduction of reactive oxygen species (ROS) and triggers apoptosis of MYCN-amplified neuroblastoma cells [2].
In vivo
Systemic BSO administration selectively altered GSH homeostasis and EAAT3 levels in the mice cerebellum. Intraperitoneal treatment of mice with 6?mmol/kg of BSO depleted GSH and GSSG in the liver at 2?h of treatment [3].
SynonymsL-Butionine sulfoximine
Chemical Properties
Molecular Weight222.31
FormulaC8H18N2O3S
Cas No.83730-53-4
SmilesCCCCS(=N)(=O)CC[C@H](N)C(O)=O
Relative Density.1.29 g/cm3
Storage & Solubility Information
Storagekeep away from moisture,store at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: Insoluble
H2O: 50 mg/mL (224.91 mM), Sonication is recommended.
Solution Preparation Table
H2O
1mg5mg10mg50mg
1 mM4.4982 mL22.4911 mL44.9822 mL224.9112 mL
5 mM0.8996 mL4.4982 mL8.9964 mL44.9822 mL
10 mM0.4498 mL2.2491 mL4.4982 mL22.4911 mL
20 mM0.2249 mL1.1246 mL2.2491 mL11.2456 mL
50 mM0.0900 mL0.4498 mL0.8996 mL4.4982 mL
100 mM0.0450 mL0.2249 mL0.4498 mL2.2491 mL

Calculator

  • Molarity Calculator
  • Dilution Calculator
  • Reconstitution Calculator
  • Molecular Weight Calculator

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

You can also refer to dose conversion for different animals. More Dose Conversion

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

Related Tags: buy L-BUTHIONINE-(S,R)-SULFOXIMINE | purchase L-BUTHIONINE-(S,R)-SULFOXIMINE | L-BUTHIONINE-(S,R)-SULFOXIMINE cost | order L-BUTHIONINE-(S,R)-SULFOXIMINE | L-BUTHIONINE-(S,R)-SULFOXIMINE chemical structure | L-BUTHIONINE-(S,R)-SULFOXIMINE in vivo | L-BUTHIONINE-(S,R)-SULFOXIMINE in vitro | L-BUTHIONINE-(S,R)-SULFOXIMINE formula | L-BUTHIONINE-(S,R)-SULFOXIMINE molecular weight