TBCA

CAS No. 934358-00-6

TBCA( Casein Kinase II Inhibitor III, TBCA )

Catalog No. M27483 CAS No. 934358-00-6

TBCA is a highly selective CK2 (casein kinase II) inhibitor, IC50 = 110 nM, Ki = 77 nM. TBCA shows selectivity for CK2 over CK1, DYRK1A and a panel of 27 other kinases.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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Biological Information

  • Product Name
    TBCA
  • Note
    Research use only, not for human use.
  • Brief Description
    TBCA is a highly selective CK2 (casein kinase II) inhibitor, IC50 = 110 nM, Ki = 77 nM. TBCA shows selectivity for CK2 over CK1, DYRK1A and a panel of 27 other kinases.
  • Description
    TBCA is a highly selective CK2 (casein kinase II) inhibitor, IC50 = 110 nM, Ki = 77 nM. TBCA shows selectivity for CK2 over CK1, DYRK1A and a panel of 27 other kinases.(In Vitro):TBCA inhibits CK2 double mutant (Val66 Ile174) with an IC50 of 0.68 μM. TBCA (0-100 μM; 24 hours) shows a drastic effect on Jurkat cells viability . TBCA dose-dependently inhibits platelet aggregation and secretion induced by various agonists including CRP, 2-MeSADP, AYPGKF and SFLLRN. TBCA also inhibits phosphorylation of PDK1, Akt, and GSK3β induced by AYPGKF.
  • In Vitro
    TBCA (0-100 μM; 24 hours) shows a drastic effect on Jurkat cells viability.TBCA also inhibits CK2 double mutant (Val66 Ile174) with an IC50 of 0.68 μM.TBCA dose-dependently inhibits platelet aggregation and secretion induced by various agonists including 2-MeSADP, AYPGKF, SFLLRN, and CRP. TBCA also inhibits phosphorylation of PDK1, Akt, and GSK3β induced by AYPGKF. Cell Viability Assay Cell Line:Jurkat cells Concentration:0-100 μM Incubation Time:24 hours Result:The viability of Jurkat cells was reduced.
  • In Vivo
    ——
  • Synonyms
    Casein Kinase II Inhibitor III, TBCA
  • Pathway
    Metabolic Enzyme/Protease
  • Target
    Casein Kinase
  • Recptor
    ——
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    934358-00-6
  • Formula Weight
    463.74
  • Molecular Formula
    C9H4Br4O2
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 100 mg/mL (215.64 mM)
  • SMILES
    C(=C/C(O)=O)\C1=C(Br)C(Br)=C(Br)C(Br)=C1
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1.Buerge IJ, et al. Stereoselective Metabolism of the Sterol Biosynthesis Inhibitor Fungicides Fenpropidin, Fenpropimorph, and Spiroxamine in Grapes, Sugar Beets, and Wheat. J Agric Food Chem. 2016 Jul 6;64(26):5301-9.
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