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• W2028376384 abstract "Previous studies have shown that BD1008 (N-[2-(3,4-dichlorophenyl)ethyl]-N-methyl-2-(1-pyrrolidinyl)ethylamine) and related analogs attenuate the toxicity and stimulant effects of cocaine through antagonism of σ receptors. In the present study, six analogs of BD1008 (UMB 98–103) were synthesized and evaluated in receptor binding and behavioral studies. Competition binding studies confirmed that all six compounds have high affinity for σ1 receptors, moderate affinity for σ2 receptors, and low to negligible affinity for monoamine transporters, opioid, N-methyl-d-aspartate, dopamine, and 5-HT receptors. In behavioral pharmacological studies, pretreatment of mice with UMB 100, UMB 101, or UMB 103 significantly attenuated cocaine-induced convulsions and lethality. Together with earlier studies, the data suggest that analogs of BD1008 are promising medication development leads for reducing the toxicity of cocaine." @default.
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• W2028376384 date "2004-05-01" @default.
• W2028376384 modified "2023-10-12" @default.
• W2028376384 title "Novel analogs of the σ receptor ligand BD1008 attenuate cocaine-induced toxicity in mice" @default.
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• W2028376384 doi "https://doi.org/10.1016/j.ejphar.2004.03.037" @default.
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