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NPT100-18A

Catalog No. T214396 Copy Product Info
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NPT100-18A is an inhibitor of α-synuclein oligomerization. It can restore cleaved caspase-3 levels to normal. NPT100-18A reduces mitochondrial oxidative stress probe levels in a compartment-specific manner and, at high concentrations, can increase ATP signaling. NPT100-18A is useful for research in Parkinson's disease (PD).

NPT100-18A

Copy Product Info
🥰Excellent
Catalog No. T214396

NPT100-18A is an inhibitor of α-synuclein oligomerization. It can restore cleaved caspase-3 levels to normal. NPT100-18A reduces mitochondrial oxidative stress probe levels in a compartment-specific manner and, at high concentrations, can increase ATP signaling. NPT100-18A is useful for research in Parkinson's disease (PD).

NPT100-18A
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For research use only—not for human use. No sales to individuals. Use as intended only.
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Product Introduction

Bioactivity
Description
NPT100-18A is an inhibitor of α-synuclein oligomerization. It can restore cleaved caspase-3 levels to normal. NPT100-18A reduces mitochondrial oxidative stress probe levels in a compartment-specific manner and, at high concentrations, can increase ATP signaling. NPT100-18A is useful for research in Parkinson's disease (PD).
In vitro
NPT100-18A (10 nM) reduces the number of Triton-X100 insoluble α-synuclein aggregates in iPSC-derived mDAN. It specifically decreases mitochondrial ROS levels in iPSC-derived mDAN without affecting overall intracellular ROS levels. At a concentration of 1 µM, NPT100-18A significantly enhances ATP signaling in iPSC-derived mDAN. Administering NPT100-18A (10 nM) over 21 days notably reduces the percentage of cCasp3⁺ neurons in iPSC-derived mDAN and inhibits early neuron apoptosis pathways associated with α-synuclein.
In vivo
NPT100-18A (1-20 mg/kg, intraperitoneally, once daily for 90 days) significantly improved motor dysfunction in mThy1-wt-α-syn transgenic mice and reduced α-syn oligomers and associated neurodegenerative pathology.
Chemical Properties
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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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:
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