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Harmine

Cat. No. M6787

All AbMole products are for research use only, cannot be used for human consumption.

Harmine Structure
Synonym:

Telepathine

Size Price Availability Quantity
100mg USD 30  USD30 In stock
500mg USD 55  USD55 In stock
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Quality Control & Documentation
Biological Activity

Harmine is a potent and selective inhibitor of DYRK1A (IC50 values are 80, 800 and 900 nM for DYRK1A, DYRK3 and DYRK2 respectively). Harmine inhibits DYRK1A-mediated tau phosphorylation and regulates PPARγ expression. Harmine also induces pancreatic beta cell proliferation. Harmine exhibits antidiabetic activity. Orally bioavailable.

Chemical Information
Molecular Weight 212.25
Formula C13H12N2O
CAS Number 442-51-3
Form Solid
Solubility (25°C) DMSO 25 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Huber, et al. Bioorg Med Chem. Identification of aquaporin 4 inhibitors using in vitro and in silico methods.

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DYRK1-IN-1 is a highly selective and ligand-efficient DYRK1A inhibitor. DYRK1-IN-1 inhibits DYRK1A phosphorylation activity with an IC50 value of 220 nM.

Dyrk1A-IN-4 

Dyrk1A-IN-4 is a potent and orally active DYRK1A and DYRK2 inhibitor with IC50s of 2 nM and 6 nM, respectively.

Woodtide

Woodtide is a substrate for the DYRK (DYRK) family of kinases whose sequence is based on that around the DYRK phosphorylation site in FKHR.

Aristolactam A IIIa

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Dyrk1A-IN-5 

Dyrk1A-IN-5 (compound 5j) is a potent and selective DYRK1A inhibitor, with an IC50 of 6 nM. Dyrk1A-IN-5 dose-dependently reduces the phosphorylation of Thr434 in SF3B1, with an IC50 of 0.5 μM. Dyrk1A-IN-5 inhibits phosphorylation of tau at Thr212, with an IC50 of 2.1 μM. Dyrk1A-IN-5 can be used for Down syndrome research.

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Keywords: Harmine, Telepathine supplier, DYRK, inhibitors, activators

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