1. MAPK/ERK Pathway Stem Cell/Wnt Neuronal Signaling Immunology/Inflammation NF-κB Metabolic Enzyme/Protease Autophagy PI3K/Akt/mTOR
  2. JNK Wnt β-catenin Amyloid-β Reactive Oxygen Species (ROS) Beclin1 GSK-3 Beta-secretase
  3. JNK3/Wnt/β-catenin modulator-1

JNK3/Wnt/β-catenin modulator-1 is a brain-penetrant JNK3 inhibitor and Wnt/β-catenin activator. JNK3/Wnt/β-catenin modulator-1 decreases 1-42 production and reduced ROS generation. JNK3/Wnt/β-catenin modulator-1 inhibits the activation of JNK and Puma, promotes Beclin-1 expression, reduces GSK-3β and BACE1 expression and activates Wnt/β-catenin signaling. JNK3/Wnt/β-catenin modulator-1 improves cognitive and memory performance, attenuates histopathological brain damage, preserves structure of hippocampal pyramidal cells and cerebral cortical neurons. JNK3/Wnt/β-catenin modulator-1 can be used for the research of Alzheimer's disease.

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JNK3/Wnt/β-catenin modulator-1

JNK3/Wnt/β-catenin modulator-1 Chemical Structure

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Description

JNK3/Wnt/β-catenin modulator-1 is a brain-penetrant JNK3 inhibitor and Wnt/β-catenin activator. JNK3/Wnt/β-catenin modulator-1 decreases 1-42 production and reduced ROS generation. JNK3/Wnt/β-catenin modulator-1 inhibits the activation of JNK and Puma, promotes Beclin-1 expression, reduces GSK-3β and BACE1 expression and activates Wnt/β-catenin signaling. JNK3/Wnt/β-catenin modulator-1 improves cognitive and memory performance, attenuates histopathological brain damage, preserves structure of hippocampal pyramidal cells and cerebral cortical neurons. JNK3/Wnt/β-catenin modulator-1 can be used for the research of Alzheimer's disease[1].

IC50 & Target[1]

GSK-3β

 

BACE1

 

JNK3

 

In Vivo

JNK3/Wnt/β-catenin modulator-1 (compound 3a) (10 mg/kg; i.p.; daily; 45 days) improves cognitive function, reduces AD-related pathological markers, and modulates key signaling pathways in an AlCl3-induced AD rat model[1].
JNK3/Wnt/β-catenin modulator-1 (10 mg/kg; i.p.; daily; 45 days) has no significant effect on normal rats[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Wister (male, 230-250 g, AlCl₃-induced AD model)[1]
Dosage: 10 mg/kg
Administration: i.p.; daily; 45 days
Result: Reduced brain amyloid beta 1-42 levels by 56.2%, JNK levels by 62.17%, Puma levels by 65.24% and ROS levels by 59.25% compared to the AlCl3-treated group.
Increased brain Beclin-1 levels by 877% compared to the AlCl3-treated group.
Upregulated mRNA expression of Wnt7a (175%), β-catenin (282%), LRP6 (330%), and FZD4 (411%) compared to the AlCl3-treated group.
Downregulated mRNA expression of GSK-3β (56%) and BACE1 (75%) compared to the AlCl3-treated group.
Improved spatial memory by reducing escape latency in Morris Water Maze, recognition memory by increasing discrimination index and ratio in Novel Object Recognition, and working memory by increasing spontaneous alternation percentage in Y-maze compared to the AlCl3-treated group.
Restored nearly normal histological structure of hippocampal pyramidal cells and cerebral cortical neurons with minimal pyknotic nuclei compared to the AlCl3-treated group.
Molecular Weight

380.42

Formula

C18H16N6O2S

SMILES

O=S(C1=CC=C(N2N=NC=C2C)C=C1)(C3=CC=C(N4N=NC=C4C)C=C3)=O

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Please store the product under the recommended conditions in the Certificate of Analysis.

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Product Name:
JNK3/Wnt/β-catenin modulator-1
Cat. No.:
HY-181160
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