A selective antagonist of σ1 receptors
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BD 1047 (hydrobromide)

Item No. 22928

Technical Information
Formal Name
N1-[2-(3,4-dichlorophenyl)ethyl]-N1,N2,N2-trimethyl-1,2-ethanediamine, dihydrobromide
CAS Number
138356-21-5
Molecular Formula
C13H20Cl2N2 • 2HBr
Formula Weight
Purity
≥98%
Formulation
A crystalline solid
PBS (pH 7.2): 10 mg/ml
SMILES
ClC1=C(Cl)C=CC(CCN(C)CCN(C)C)=C1.Br.Br
InChi Code
InChI=1S/C13H20Cl2N2.2BrH/c1-16(2)8-9-17(3)7-6-11-4-5-12(14)13(15)10-11;;/h4-5,10H,6-9H2,1-3H3;2*1H
InChi Key
WOALTFHGLDVJHK-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    BD 1047 is a selective antagonist of sigma-1 (σ1) receptors (Ki = 0.9 nM in a radioligand binding assay).1 It is selective for σ1 receptors with binding affinity values greater than 10,000 nM for human recombinant dopamine, opioid, PCP, and serotonin receptors in vitro. In vivo, pretreatment with BD 1047 protects against convulsions and lethality induced by cocaine (Item Nos. 16186 | ISO60176) and reduces cocaine-induced locomotor activity. It reduces dystonias induced by the σ receptor agonists haloperidol (Item No. 12014) and di-o-tolylguanidine (DTG) in rats in a dose-dependent manner.2 In vivo administration of BD 1047 also attenuates mechanical allodynia and microglial activation in a rat model of bone cancer pain.3

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. McCracken, K.A., Bowen, W.D., de Costa, B.R., et alTwo novel σ receptor ligands, BD1047 and LR172, attenuate cocaine-induced toxicity and locomotor activity. Eur. J. Pharmacol. 370(3), 225-232 (1999).

    2. Matsumoto, R.R., Bowen, W.D., Tom, V.A., et alCharacterization of two novel σ receptor ligands: antidystonic effects in rats suggest σ receptor antagonism. Eur. J. Pharmacol. 280(3), 301-310 (1995).

    3. Zhu, S., Wang, C., Han, Y., et alSigma-1 receptor antagonist BD1047 reduces mechanical allodynia in a rat model of bone cancer pain through the inhibition of spinal NR1 phosphorylation and microglia activation. mediators Inflamm. 2015, 265056 (2015).