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BD-1047

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
BD-1047
Clinical data
ATC code
  • none
Identifiers
  • N'-[2-(3,4-dichlorophenyl)ethyl]-N,N,N'-trimethylethane-1,2-diamine
CAS Number
PubChemCID
IUPHAR/BPS
ChemSpider
UNII
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC13H20Cl2N2
Molar mass275.22 g·mol−1
3D model (JSmol)
  • Clc1ccc(CCN(C)CCN(C)C)cc1Cl
  • InChI=1S/C13H20Cl2N2/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 checkY
  • Key:MGVRNMUKTZOQOW-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

BD-1047 is asigma receptorantagonist, selective for theσ1 subtype. It has effects in animal studies suggestive ofantipsychotic activity and may also be useful in the treatment ofneuropathic pain.[1][2]

More recent studies also suggest a novel role for BD-1047 in attenuatingethanol-inducedneurotoxicityin vitro, and additional research is being conducted on this compound as a possible pharmacotherapy for alcohol use disorder (AUD)[3]

References

[edit]
  1. ^Skuza G, Rogóz Z (2006). "Effect of BD 1047, a sigma1 receptor antagonist, in the animal models predictive of antipsychotic activity".Pharmacological Reports.58 (5):626–35.PMID 17085854.
  2. ^Roh DH, Kim HW, Yoon SY, Seo HS, Kwon YB, Kim KW, Han HJ, Beitz AJ, Na HS, Lee JH (November 2008)."Intrathecal injection of the sigma(1) receptor antagonist BD1047 blocks both mechanical allodynia and increases in spinal NR1 expression during the induction phase of rodent neuropathic pain".Anesthesiology.109 (5):879–89.doi:10.1097/ALN.0b013e3181895a83.PMID 18946301.
  3. ^Reynolds AR, Saunders MA, Prendergast MA (2016)."Ethanol Stimulates Endoplasmic Reticulum Inositol Triphosphate and Sigma Receptors to Promote Withdrawal-Associated Loss of Neuron-Specific Nuclear Protein/Fox-3".Alcohol Clin Exp Res.40 (7):1454–61.doi:10.1111/acer.13097.PMC 6662182.PMID 27177604.
σ1
σ2
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