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Nurr1 agonist 12

Nurr1 agonist 12 (Compound 37) is the agonist for nuclear receptor-associated protein 1 (Nurr1) that activates the transcriptional activity of Nurr1 with an EC50 of 0.06 μM. Nurr1 agonist 12 activates the human response elements NBRE, NurRE, and DR5 with EC50 of 0.07 μM, 0.027 μM, and 0.014 μM, respectively. Nurr1 agonist 12 induces the expression of Nurr1-regulated neurotrophic genes, such as tyrosine hydroxylase (TH), SOD1/2, BDNF, Sestrin 3, and BIRC5 (Survivin) . Nurr1 agonist 12 exhibits neuroprotective efficacy against Paraquat-induced neurotoxicity[1].

Product Specifications

UNSPSC

12352005

Target

Nuclear Hormone Receptor 4A/NR4A

Related Pathways

Vitamin D Related/Nuclear Receptor

Applications

Neuroscience-Neuromodulation

Field of Research

Neurological Disease

Purity

99.62

Solubility

DMSO : 100 mg/mL (ultrasonic)

Smiles

O=C(C1=C(Cl)C=C2C=CNC2=C1)NC3=CC4=C(C=CC=C4)N=C3

Molecular Formula

C18H12ClN3O

Molecular Weight

321.76

References & Citations

[1]Egner M, et al., A Nurr1 Agonist Derived from the Natural Ligand DHI Induces Neuroprotective Gene Expression. J Med Chem. 2025 Feb 27;68 (4) :4829-4847.

Shipping Conditions

Room Temperature

Storage Conditions

-20°C, 3 years; 4°C, 2 years (Powder)

Scientific Category

Reference compound1

Clinical Information

No Development Reported

Isoform

Nurr1/NR4A2

Available Sizes

Curated Selection

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