AdipoGen Life Sciences

DYRK1A/B Inhibitor AnnH31

CHF 180.00
In stock
AG-CR1-3650-C500500 µgCHF 180.00
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Product Details
Synonyms 2-(7-Methoxy-1-methyl-9H-pyrido[3,4-b]indol-9-yl)acetonitrile; AnnH31
Product Type Chemical
Properties
Formula

C15H13N3O

MW 251.3
CAS 241809-12-1
Purity Chemicals ≥98% (HPLC, NMR)
Appearance Off-white to tan solid.
Solubility Soluble in DMSO.
Identity Determined by 1H-NMR.
Other Product Data

DMSO Stock Solution: Prior to performing biological experiments the DMSO stock solution should be further diluted into water or other aqueous buffers to ensure that the residual amount of DMSO is insignificant, since DMSO may have physiological effects at high concentrations.

InChi Key FCFDJQKAPLIDTQ-UHFFFAOYSA-N
Smiles CC1=NC=CC2=C1N(CC#N)C3=CC(OC)=CC=C32
Shipping and Handling
Shipping AMBIENT
Short Term Storage +4°C
Long Term Storage -20°C
Handling Advice Keep cool and dry.
Protect from light and moisture.
Use/Stability Stable for at least 2 years after receipt when stored at -20°C.
Documents
MSDS Download PDF
Product Specification Sheet
Datasheet Download PDF
Description
  • Potent selective membrane-permeable DYRK1A (IC50=81nM) and DYRK1B inhibitor. Off-target inhibition of CLK1 and slightly DYRK2 and HIPK2.
  • Shows minimal inhibitory effects on monoamine oxidase A (MAO A) (IC50=3.2µg), with 40-fold selectivity for DYRK1A over MAO A.
  • Dose-dependently reduced the phosphorylation of three known DYRK1A substrates (SF3B1, SEPT4 and tau) without negative effects on cell viability in celular assays.
  • Shows cytotoxic effects in HeLa cells at high concentrations (3-10µM).
  • The pleiotropic protein kinase DYRK1A has diverse functions in cell cycle control, neuronal differentiation and synaptic transmission and has attracted increasing interest as a potential drug target, due to its role in the pathology of Down syndrome, neurodegenerative diseases such as Alzheimer's disease and cancer. The closely related kinase DYRK1B has been associated with cancer cell survival by arresting cells in a quiescent state to allow cellular repair and mutations in DYRK1B might be causative in metabolic syndrome.
Product References
  1. Selectivity profiling and biological activity of novel beta-carbolines as potent and selective DYRK1 kinase inhibitors: K. Ruben, et al.; PLos One 10, e0132453 (2015)
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