BD 1008 dihydrobromide
Chemical Name: N-[2-(3,4-Dichlorophenyl)ethyl]-N-methyl-2-(1-pyrrolidinyl)ethylamine dihydrobromide
Biological Activity
Potent and selective σ-ligand (Ki against [3H]-(+)-3-PPP = 0.34 nM).Technical Data
The technical data provided above is for guidance only.
For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.
Background References
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High-throughput genotoxicity assay identifies antioxidants as inducers of DNA damage response and cell death.
Fox JT, Sakamuru S, Huang R
Proc. Natl. Acad. Sci. U.S.A., 2012;109(14):5423-8. -
Antagonism of N-MthD.-aspartate receptors by σ site ligands: potency, subtype-selectivity and mechanisms of inhibition.
Whittemore et al.
J.Pharmacol.Exp.Ther., 1997;282:326 -
Synthesis, characterization, and biological evaluation of a novel class of N-(arylethyl)-N-alkyl-2-(1-pyrrolidinyl)ethylamines - structural requirements and binding affinity at the σ receptor.
De Costa et al.
J.Med.Chem., 1992;35:38 -
Differentiation of σ ligand-activated receptor subtypes that modulate NMDA-evoked [3H]-noradrenaline release in rat hippocampal slices.
Monnet et al.
Br.J.Pharmacol., 1996;119:65
Product Datasheets
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Citations for BD 1008 dihydrobromide
The citations listed below are publications that use Tocris products. Selected citations for BD 1008 dihydrobromide include:
2 Citations: Showing 1 - 2
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Stimulants as specific inducers of DA-independentσ agonist self-administration in rats.
Authors: Hiranita Et al.
Neurochem Int 2013;347:42633
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Decreases in cocaine self-administration with dual inhibition of the DA transporter and σ receptors.
Authors: Hiranita Et al.
J Pharmacol Exp Ther 2011;339:662
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