>>Signaling Pathways>> PI3K/Akt/mTOR Signaling>> CK2>>TBCA

TBCA (Synonyms: Casein Kinase II Inhibitor III,Tetrabromocinnamic Acid)

Catalog No.GC14181

TBCA는 IC50이 110nM이고 Ki가 77nM인 고도로 선택적인 CK2(카제인 키나제 II) 억제제입니다. TBCA는 CK1, DYRK1A 및 27개의 다른 키나제의 패널보다 CK2에 대한 선택성을 보여줍니다.

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TBCA Chemical Structure

Cas No.: 934358-00-6

Size 가격 재고 수량
1mg
US$50.00
재고 있음
5mg
US$157.00
재고 있음
10mg
US$292.00
재고 있음
25mg
US$663.00
재고 있음

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Sample solution is provided at 25 µL, 10mM.

Description Chemical Properties Product Documents Related Products

Tetrabromocinnamic Acid (TBCA) is a new class of specific protein kinase CK2 inhibitors [1].

Protein kinases have been involved in catalyzing the phosphorylation of serine, threonine and tyrosine residues in protein substrates that play dominant roles in controlling nearly all cellular functions. The Ser/Thr-specific protein kinase CK2 has been implicated in signal transduction, gene expression, DNA repair, RNA and protein synthesis. CK2 is invariably elevated in a wide spectrum of tumours [1].

In vitro: TBCA was a selective, cell-permeable inhibitor of CK2 with an IC50 of 0.11 μM. The Ki value was 77 nM. TBCA showed minimal effect on a panel of 28 other kinases. TBCA induced cell death in Jurkat adult T cell leukemia cells with an DC50 of 7.7 μM [1]. TBCA dose-dependently inhibited platelet aggregation and secretion induced by various agonists including 2-MeSADP, AYPGKF, SFLLRN, and CRP [2]. TBCA also significantly inhibited agonist-induced thromboxane A2 (TxA2) generation and ERK phosphorylation. TBCA significantly inhibited platelet spreading on immobilized fibrinogen surface and clot retraction mediated by integrin αIIbβ3 signaling [2].

References:
[1] Pagano M A, Poletto G, Di Maira G, et al.  Tetrabromocinnamic acid (TBCA) and related compounds represent a new class of specific protein kinase CK2 inhibitors[J]. Chembiochem, 2007, 8(1): 129-139.
[2] Ryu S Y, Kim S.  Evaluation of CK2 inhibitor (E)-3-(2, 3, 4, 5-tetrabromophenyl) acrylic acid (TBCA) in regulation of platelet function[J]. European journal of pharmacology, 2013, 720(1): 391-400.

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