BAMB-4 (Synonyms: ITPKA-IN-C14) |
| Catalog No.GC14668 |
BAMB-4 (ITPKA-IN-C14) es un inhibidor de ITPKA especÍfico y permeable a la membrana. BAMB-4 tiene alta estabilidad y permeabilidad de la membrana y frente a la actividad quinasa de inositol-1,4,5-trisfosfato (InsP3) de inositol-1,4,5-trisfosfato-3-quinasa A (ITPKA) con un valor IC50 de 20 μM. BAMB-4 se puede utilizar para la investigaciÓn de metÁstasis de cÁncer de pulmÓn.
Products are for research use only. Not for human use. We do not sell to patients.
Cas No.: 891025-25-5
Sample solution is provided at 25 µL, 10mM.
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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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