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Chemical Structure
Chemical Structure
Chemical Structure

DYRK1A/B Inhibitor AnnH31 [241809-12-1]

Research Use Only
AG-CR1-3650
AdipoGen Life Sciences
CAS Number241809-12-1
Product group Chemicals
Estimated Purity>98%
Molecular Weight251.3
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Packing Size
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Overview

  • Supplier
    AdipoGen Life Sciences
  • Product Name
    DYRK1A/B Inhibitor AnnH31 [241809-12-1]
  • Delivery Days Customer
    10
  • CAS Number
    241809-12-1
  • Certification
    Research Use Only
  • Estimated Purity
    >98%
  • Hazard Information
    Warning
  • Molecular Formula
    C15H13N3O
  • Molecular Weight
    251.3
  • Scientific Description
    Chemical. CAS: 241809-12-1. Formula: C15H13N3O. MW: 251.3. Synthetic. 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=3.2microg), 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 (3-10microM). 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 Alzheimers 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. - 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=3.2microg), 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 (3-10microM). 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 Alzheimers 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.
  • SMILES
    CC1=NC=CC2=C1N(CC#N)C3=CC(OC)=CC=C32
  • Storage Instruction
    -20°C,2°C to 8°C
  • UNSPSC
    51202000

References

  • 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)