Debromohymeni<wbr/>aldisine

Debromohymenialdisine

CAT N°: 14873
Price:

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}

Territorial Availability: Available through Bertin Technologies only in France

  • Synonyms
    • (4Z)-4-(2-amino-1,5-dihydro-5-oxo-4H-imidazol-4-ylidene)-4,5,6,7-tetrahydro-pyrrolo[2,3-c]azepin-8(1H)-one
  • Correlated keywords
    • 96562-99-1 natural products inhibitors inhibits inhibitions kinases cells cycles DNA damages Chks Chk-1 Chk-2 Chk1 Chk2 1 2 one two checkpoint kinases marine sponge alkaloids blocks blockage blocking G2 arrest repairs regulation regulates regulated MAP kinases 1 MEK-1 MEK1 MEKs glycogen synthase kinase-3b GSK-3b kinase-3beta kinase-3.beta. kinase-3 ? K-3 ? K-3.beta. K-3beta K-3b GSKs cyclin-dependent cyclin dependent 5 five p25 CDKs Cdk5 Cdk-5 protein tyrosine 6 Brk SKF108753 SKF-108753 SKFs 108753 Z-debromohymenialdisine 96562-99-1 humans sensor signals checkpoints ataxia telangiectasia mutated ATM ATM-Tad2 Tad2 MAP
  • Product Overview:
    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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