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BAMB-4 (Synonyms: ITPKA-IN-C14)

カタログ番号GC14668

BAMB-4 (ITPKA-IN-C14) は、特異的で膜透過性の ITPKA 阻害剤です。 BAMB-4 は高い安定性と膜透過性を持ち、IC50 値が 20 のイノシトール-1,4,5-三リン酸-3-キナーゼ A (ITPKA) のイノシトール-1,4,5-三リン酸 (InsP3) キナーゼ活性に対してμM。 BAMB-4 は、肺がんの転移の研究に使用できます。

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BAMB-4 化学構造

Cas No.: 891025-25-5

サイズ 価格 在庫数 個数
10mM (in 1mL DMSO)
$196.00
在庫あり
5mg
$227.00
在庫あり
10mg
$345.00
在庫あり

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Sample solution is provided at 25 µL, 10mM.

Description Chemical Properties Product Documents Related Products

BAMB-4 is an inhibitor of inositol-1,4,5-trisphosphate-3-kinase A (ITPKA) with an IC50 value of 20 µM [1].

ITPKA is an InsP3 kinase. It binds to actin filaments and bundles them. This protein regulates actin dynamics as well as inositol phosphate signaling [1].

BAMB-4 was almost completely taken up by H1299 cells. BAMB-4 did not belong to typical kinase inhibitors. Its relatively high specificity and high cellular uptake provide the possibility to effectively inhibit InsP3 kinase in vivo. Among InsP3Kinase inhibitors, BAMB-4 exhibit the lowest inhibition frequency. BAMB-4 showed an inhibitory effect only in 1 from 42 tested targets. There was no detected BAMB-4 target in kinase screens. These results indicated that BAMB-4 is not a typical kinase inhibitor. In vitro, data showed that BAMB-4 increased Km and reduced Vmax with respect to InsP3. BAMB-4 at the lowest concentration (10 µM) increased the Km-value for InsP3 by 160%. BAMB-4 at elevated concentrations did not further rise the Km-value for InsP3. BAMB-4 dose-dependently decreased Vmax from 75% to 50%. Decreased Vmax and increased Km in presence of inhibitor indicated that BAMB-4 might belong to mixed type inhibitors. Data showed that BAMB-4 also reduced Vmax and increased Km with respect to ATP [2].

There is still no any available result of the application of BAMB-4 in animals.

References:
[1].  Schrder D, Tdter K, Gonzalez B, et al. The new InsP 3 Kinase inhibitor BIP-4 is competitive to InsP 3 and blocks proliferation and adhesion of lung cancer cells. Biochemical pharmacology, 2015, 96(2): 143-150.
[2].  Schrder D, Rehbach C, Seyffarth C, et al. Identification of a new membrane-permeable inhibitor against inositol-1, 4, 5-trisphosphate-3-kinase A. Biochemical and biophysical research communications, 2013, 439(2): 228-234.

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