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Takinib (Synonyms: EDHS-206)

Katalog-Nr.GC32687

Takinib (EDHS-206) ist ein oral aktiver und selektiver TAK1-Inhibitor (IC50 = 9,5 nM), mehr als 1,5 log stÄrker als die zweit- und drittplatzierten Ziele, IRAK4 (120 nM) bzw. IRAK1 (390 nM).

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Takinib Chemische Struktur

Cas No.: 1111556-37-6

Größe Preis Lagerbestand Menge
10mM (in 1mL DMSO)
79,00 $
Auf Lager
1mg
43,00 $
Auf Lager
5mg
111,00 $
Auf Lager
10mg
139,00 $
Auf Lager
50mg
556,00 $
Auf Lager
100mg
1.020,00 $
Auf Lager

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Sample solution is provided at 25 µL, 10mM.

Description Protocol Chemical Properties Product Documents Related Products

Takinib is a potent and selective TAK1 inhibitor with an IC50 of 9.5 nM.

At 10 mM, Takinib shows significant inhibitory activity (<10% enzyme activity after exposure) on six serine/threonine kinases, including TAK1, IRAK4, IRAK1, GCK, CLK2, and MINK1. Analysis reveals that increasing concentrations of Takinib leads to a decrease in Vmax while maintaining KM. When the enzyme is activated with 5 mM ATP for 3 hr, the same Vmax is reached for 0, 10, 50, and 100 nM Takinib, and KM increases for these concentrations, which implies that Takinib is an ATP-competitive inhibitor if TAK1 is ATP activated. Importantly, results show that Takinib inhibits the function of both activated and un-activated TAK1 with identical potency. TNF-α stimulation in the presence of Takinib induces caspase activity in MDA-MB-231 cells in a dose-dependent manner, whereas unstimulated cells do not upregulate caspase activity. Takinib reduces phosphorylation significantly but does not influence total protein levels. Takinib inhibits phosphorylation of IKK, MAPK 8/9, and c-Jun in a dose-dependent manner. Takinib shows an almost complete inhibition of IL-6 secretion at micromolar concentrations following 24 hr of treatment in the presence of TNF-α[1].

[1]. Totzke J, et al. Takinib, a Selective TAK1 Inhibitor, Broadens the Therapeutic Efficacy of TNF-α Inhibition for Cancer and Autoimmune Disease. Cell Chem Biol. 2017 Aug 17;24(8):1029-1039.

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