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LY231617

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Catalog No. T22942Cas No. 141545-89-3
Alias LY-231617

LY231617 is an orally bioavailable, blood-brain barrier-penetrant antioxidant that mitigates systemic ischaemic neuronal injury in rats. It exerts neuroprotective effects against H₂O₂-induced toxicity by inhibiting lipid peroxidation.

LY231617

LY231617

😃Good
Purity: 97.48%
Catalog No. T22942Alias LY-231617Cas No. 141545-89-3
LY231617 is an orally bioavailable, blood-brain barrier-penetrant antioxidant that mitigates systemic ischaemic neuronal injury in rats. It exerts neuroprotective effects against H₂O₂-induced toxicity by inhibiting lipid peroxidation.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$32-In Stock
5 mg$73-In Stock
10 mg$113-In Stock
25 mg$239-In Stock
50 mg$347-In Stock
100 mg$538-In Stock
1 mL x 10 mM (in DMSO)$80-In Stock
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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.
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Purity:97.48%
Appearance:Solid
Color:Yellow
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Product Introduction

Bioactivity
Description
LY231617 is an orally bioavailable, blood-brain barrier-penetrant antioxidant that mitigates systemic ischaemic neuronal injury in rats. It exerts neuroprotective effects against H₂O₂-induced toxicity by inhibiting lipid peroxidation.
In vitro
After co-incubation with hippocampal cells overnight, LY231617 (0.25-25 μM) attenuated the toxicity of H₂O₂ on hippocampal cell cultures, with the most significant effect observed at 10 μM [1].
Overnight incubation with LY231617 (5 μM) inhibited prostaglandin production in 8-parazacco spilurus subsp. spilurus and prevented glutathione depletion [1].
In vivo
In the rat four-vessel occlusion model, LY231617 (50 mg/kg) administered orally 30 minutes before ischemia significantly alleviated neuronal damage [2]. LY231617 (20 mg/kg) administered intravenously 30 minutes after ischemia effectively protected the hippocampus and striatum from damage caused by four-vessel occlusion [2].
SynonymsLY-231617
Chemical Properties
Molecular Weight299.88
FormulaC17H30ClNO
Cas No.141545-89-3
SmilesCl.OC=1C(=CC(=CC1C(C)(C)C)CNCC)C(C)(C)C
Relative Density.no data available
Storage & Solubility Information
Storagestore under nitrogen | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 200 mg/mL (666.93 mM), Sonication is recommended.
Ethanol: <29.99 mg/mL, Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 5 mg/mL (16.67 mM), Sonication is recommended.
Please add the solvents sequentially, clarifying the solution as much as possible before adding the next one. Dissolve by heating and/or sonication if necessary. Working solution is recommended to be prepared and used immediately. The formulation provided above is for reference purposes only. In vivo formulations may vary and should be modified based on specific experimental conditions.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.3347 mL16.6733 mL33.3467 mL166.7334 mL
5 mM0.6669 mL3.3347 mL6.6693 mL33.3467 mL
10 mM0.3335 mL1.6673 mL3.3347 mL16.6733 mL
20 mM0.1667 mL0.8337 mL1.6673 mL8.3367 mL
50 mM0.0667 mL0.3335 mL0.6669 mL3.3347 mL
100 mM0.0333 mL0.1667 mL0.3335 mL1.6673 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:
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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

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