BDE 77 505G/ML IN NONANE OEKANAL (C15-1631-904)

General description

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.

Biochem/physiol Actions

Primary Target
H+-ATPase

Target IC₅₀: 22 µM in suppressing short circuit current

Warning

Toxicity: Corrosive (L)

Reconstitution

Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.

Other Notes

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.

Legal Information

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