Shanghai Institute of Pharmaceutical Industry, 1111 North Zhongshan Road, Shanghai 200437, PR China.
Bioorg Med Chem Lett. 2010 Feb 1;20(3):1256-9. doi: 10.1016/j.bmcl.2009.11.108. Epub 2009 Nov 27.
Four optical isomers of SIPI5056 were synthesized and evaluated for their antidepressant activities and acute toxicities as novel multiple reuptake inhibitors of monoamine transmitters. Chiral alanines were used as educts to prepare their respective target compounds in nine steps. Pharmacological results showed that the (1R,2S)-SIPI5056 isomer has higher inhibitory activity and lower toxicity than other three isomers and is worthy of further development.
四种 SIPI5056 的对映异构体被合成并评估了它们作为单胺递质的新型多摄取抑制剂的抗抑郁活性和急性毒性。手性丙氨酸被用作原料,通过九步反应制备各自的目标化合物。药理结果表明,(1R,2S)-SIPI5056 对映异构体比其他三种异构体具有更高的抑制活性和更低的毒性,值得进一步开发。