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Tau Protein Phosphorylation-IN-1

Catalog No. T213552 Copy Product Info
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Tau ProteinPhosphorylation-IN-1 is a tau protein phosphorylation inhibitor that effectively protects PC12 cells from Aβ25-35-induced cytotoxicity (EC50 = 1.93 μM) and is capable of crossing the blood-brain barrier. It reverses tau protein hyperphosphorylation both in vitro and in vivo, significantly suppresses the expression of immune-related cytotoxic factors, blocks the MAPK and NF-κB signaling pathways, and reduces the levels of RAGE and apoptosis factor Bax/Bcl-2. In Alzheimer's disease mouse models, Tau ProteinPhosphorylation-IN-1 alleviates neuronal damage and improves learning and memory capabilities. It is applicable for Alzheimer's disease research.

Tau Protein Phosphorylation-IN-1

Copy Product Info
🥰Excellent
Catalog No. T213552

Tau ProteinPhosphorylation-IN-1 is a tau protein phosphorylation inhibitor that effectively protects PC12 cells from Aβ25-35-induced cytotoxicity (EC50 = 1.93 μM) and is capable of crossing the blood-brain barrier. It reverses tau protein hyperphosphorylation both in vitro and in vivo, significantly suppresses the expression of immune-related cytotoxic factors, blocks the MAPK and NF-κB signaling pathways, and reduces the levels of RAGE and apoptosis factor Bax/Bcl-2. In Alzheimer's disease mouse models, Tau ProteinPhosphorylation-IN-1 alleviates neuronal damage and improves learning and memory capabilities. It is applicable for Alzheimer's disease research.

Tau Protein Phosphorylation-IN-1
Cas No. 3075165-36-2
Pack SizePriceUSA StockGlobal StockQuantity
10 mgInquiry10-14 weeks10-14 weeks
50 mgInquiry10-14 weeks10-14 weeks
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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With extensive experience in compound synthesis, we can provide rapid custom synthesis services for this product according to your research needs.
For research use only—not for human use. No sales to individuals. Use as intended only.
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Product Introduction

Bioactivity
Description
Tau ProteinPhosphorylation-IN-1 is a tau protein phosphorylation inhibitor that effectively protects PC12 cells from Aβ25-35-induced cytotoxicity (EC50 = 1.93 μM) and is capable of crossing the blood-brain barrier. It reverses tau protein hyperphosphorylation both in vitro and in vivo, significantly suppresses the expression of immune-related cytotoxic factors, blocks the MAPK and NF-κB signaling pathways, and reduces the levels of RAGE and apoptosis factor Bax/Bcl-2. In Alzheimer's disease mouse models, Tau ProteinPhosphorylation-IN-1 alleviates neuronal damage and improves learning and memory capabilities. It is applicable for Alzheimer's disease research.
In vitro
Tau Protein Phosphorylation-IN-1 (compound B1) shows no toxicity to PC12 cells at a concentration of 30 μM for 24 hours and effectively counters Aβ 25-35-induced cytotoxicity at 10 μM. In PC12 cells exposed to Aβ 25-35, Tau Protein Phosphorylation-IN-1 (2.5-10 μM, 24 hours) exhibits neuroprotective effects through various mechanisms. It significantly reduces tau phosphorylation at Thr181, Thr205, and Ser396 sites, inhibits the phosphorylation of MAPKs (p38, ERK, JNK) and NF-κB, reverses Aβ-induced upregulation of iNOS and COX-2 expression, regulates apoptosis-related proteins Bax/Bcl-2 expression, and suppresses RAGE.
In vivo
Tau Protein Phosphorylation-IN-1, administered intraperitoneally at doses of 2.5, 5, and 10 mg/kg once daily for 28 days, effectively enhances cognitive function, reduces excessive tau protein phosphorylation, and suppresses neuroinflammation in a mouse model of Alzheimer's disease.
Chemical Properties
Molecular Weight628.9
FormulaC39H56N4O3
Cas No.3075165-36-2
SmilesC(OCCN1C(=NN=N1)C2=CC=CC=C2)(=O)[C@]34[C@](C=5[C@@](C)(CC3)[C@@]6(C)[C@](CC5)([C@]7(C)[C@@](CC6)(C(C)(C)[C@@H](O)CC7)[H])[H])(CC(C)(C)CC4)[H]
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:
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