A cell-permeable, benzyl amine compound that can cross the blood-brain barrier and act as a selective antagonist of Sigma-2/progesterone receptor membrane component 1 (PGRMC1) receptor. Shown to competitively displace selective radioligand (3H-DTG) from homogenates of human B cell lines (Ki = 48 nM). Effectively blocks the effects of Abeta on membrane trafficking (EC50 = 8.7 µM) and displaces Abeta binding on cultured neurons (EC50 = 3.9 µM). It can also reverse Abeta oligomer-mediated trafficking deficits (EC50 = 7.3 µM) and restore normal synaptic function and cognitive abilities in a murine model of Alzheimer′s disease (10 - 30 mg/kg. p.o. over a period of 5.5 months). Shown to be effective when added either 1 hour prior to or 1 hour after Abeta oligomer preparations.
Please note that the molecular weight for this compound is batch-specific due to variable water content. Please refer to the vial label or the certificate of analysis for the batch-specific molecular weight. The molecular weight provided represents the baseline molecular weight without water.
Biochem./physiol. Wirkung
Primary Target Sigma-2
Verpackung
Packaged under inert gas
Warnhinweis
Toxicity: Standard Handling (A)
Rekonstituierung
Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.
Sonstige Hinweise
Izzo, P.M., et al. 2014. Plos One.9, e111898.
Rechtliche Hinweise
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
Lagerklassenschlüssel
11 - Combustible Solids
WGK
WGK 3
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
Analysenzertifikate (COA)
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