Sulfhydryl alkylating reagent that inhibits H+-ATPase and suppresses the short circuit current (IC50 = 22 µM) in pancreatic duct cells. Inactivates NADP-dependent isocitrate dehydrogenase. Also a potent inhibitor of both Mg2+ and Ca2+/Mg2+-stimulated DNA fragmentation in rat liver nuclei. Stimulates arachidonic acid release through activation of PLA2 in endothelial cells.
Sulfhydryl alkylating reagent. Has been used for blocking sulfhydryl containing reagents which interfere with glucose oxidase assays. Inactivates NADP-dependent isocitrate dehydrogenase. Endonuclease inhibitor. Also a potent inhibitor of both Mg2+ and Ca2+/Mg2+-stimulated DNA fragmentation in rat liver nuclei.
生物化学的/生理学的作用
Primary Target H+-ATPase
Target IC50: 22 µM in suppressing short circuit current
警告
Toxicity: Corrosive (L)
再構成
Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.
その他情報
Huang, Y.C., et al. 1995. Arch. Biochem. Biophys. 316, 485. Neve, E.P.A., et al. 1995. Biochem. Pharmacol. 49, 57. Cain, K., et al. 1994. Biochem. Cell Biol.72, 631. Banger, K.K., et al. 1993. Biochem. J. 290, 199. Mattingly, J.R., Jr., et al. 1993. J. Biol. Chem. 268, 3925.
法的情報
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany