Debromohymeni<wbr/>aldisine

Debromohymenialdisine

CAT N°: 14873
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177.00 150.45

Damaged DNA in humans is detected by sensor proteins that transmit a signal through checkpoint kinases (Chks) Chk1 and Chk2.{24026} Debromohymenialdisine (DBH) is a marine sponge alkaloid that inhibits Chk1 and Chk2 (IC50 = 3 and 3.5 µM, respectively), blocking G2 arrest.{24024,24029} Because it does not significantly affect the activity of ataxia-telangiectasia mutated (ATM) or ATM-Tad2-related protein, DBH is a useful tool for studying the roles of Chk1 and Chk2 in DNA repair and cell cycle regulation.{24024} DBH also inhibits MAP kinase kinase 1 (IC50 = 881 nM), glycogen synthase kinase 3? (IC50 = 1.39 ?M), cyclin-dependent kinase 5/p25 (IC50 = 9.12 ?M), protein tyrosine kinase 6 (IC50 = 0.6 ?M), and other kinases largely unrelated to DNA damage/repair and cell cycling.{24027,24028,24025,24023}

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