Stereoselective Potencies and Relative Toxicities of 纬-Coniceine and N-Methylconiine Enantiomers
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纬-Coniceine, coniine, and N-methylconiine are toxic alkaloids present in poison hemlock (Conium maculatum). We previously reported the comparison of the relative potencies of (+)- and (-)-coniine enantiomers. In this study, we synthesized 纬-coniceine and the enantiomers of N-methylconiine and determined the biological activity of 纬-coniceine and each of the N-methylconiine enantiomers in vitro and in vivo. The relative potencies of these piperidine alkaloids on cells expressing human fetal muscle-type nicotinic acetylcholine receptors had the rank order of 纬-coniceine > (鈭?-N-methylconiine > (卤)-N-methylconiine > (+)-N-methylconiine. The relative lethalities of 纬-coniceine and (鈭?-, (卤)-, and (+)-N-methylconiine in vivo using a mouse bioassay were 4.4, 16.1, 17.8, and 19.2 mg/kg, respectively. The results from this study suggest 纬-coniceine is a more potent agonist than the enantiomers of N-methylconiine and that there is a stereoselective difference in the in vitro potencies of the enantiomers of N-methylconiine that correlates with the relative toxicities of the enantiomers in vivo.
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