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Chemical Structure
Chemical Structure
Chemical Structure

DMAT [749234-11-5]

Research Use Only
AG-CR1-3654
AdipoGen Life Sciences
CAS Number749234-11-5
Product group Chemicals
Estimated Purity>96%
Molecular Weight476.8
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Overview

  • Supplier
    AdipoGen Life Sciences
  • Product Name
    DMAT
  • Delivery Days Customer
    10
  • CAS Number
    749234-11-5
  • Certification
    Research Use Only
  • Estimated Purity
    >96%
  • Hazard Information
    Warning
  • Molecular Formula
    C9H7Br4N3
  • Molecular Weight
    476.8
  • Scientific Description
    Chemical. CAS: 749234-11-5. Formula: C9H7Br4N3. MW: 476.8. Synthetic. Potent high affinity ATP-competitive inhibitor of casein kinase II (CK2) (IC50=0.13microM). Inhibits CK2 in rat liver with >1000-fold greater selectivity for CK2 than for CK1 (IC50=140nM and >200 microM, respectively). DYRK1A and DYRK2 inhibitor (IC50= ~0.4microM for both). Shown to inhibit additional kinases, such as PIM1, PIM3, HIPK2, HIPK3, PKD1 and CDK2 in the submicromolar range. Anticancer agent. Apoptosis inducer in different cancer cell lines. Induces reactive oxygen species (ROS) and DNA double strand breaks in tumor cells. Induces apoptosis in cells expressing an inhibitor-resistant CK2, by inhibiting quinone reductase 2 (NQO2), binding with similar affinities to the oxidized and reduced forms of NQO2. Useful for in vivo studies due to cell permeability and high efficacy in cultured cells and implications in research and treatment of neoplasia and infective diseases, in which CK2 plays a role. - Potent high affinity ATP-competitive inhibitor of casein kinase II (CK2) (IC50=0.13microM). Inhibits CK2 in rat liver with >1000-fold greater selectivity for CK2 than for CK1 (IC50=140nM and >200 microM, respectively). DYRK1A and DYRK2 inhibitor (IC50= ~0.4microM for both). Shown to inhibit additional kinases, such as PIM1, PIM3, HIPK2, HIPK3, PKD1 and CDK2 in the submicromolar range. Anticancer agent. Apoptosis inducer in different cancer cell lines. Induces reactive oxygen species (ROS) and DNA double strand breaks in tumor cells. Induces apoptosis in cells expressing an inhibitor-resistant CK2, by inhibiting quinone reductase 2 (NQO2), binding with similar affinities to the oxidized and reduced forms of NQO2. Useful for in vivo studies due to cell permeability and high efficacy in cultured cells and implications in research and treatment of neoplasia and infective diseases, in which CK2 plays a role.
  • SMILES
    CN(C)C1=NC2=C(Br)C(Br)=C(Br)C(Br)=C2N1
  • Storage Instruction
    -20°C,2°C to 8°C
  • UNSPSC
    51202000