The Synthesis and Analgesic Activities of Some Spiro[indan-l,3'-pyrrolidine] Derivatives Designed as Rigid Analogs of Profadol
作者:P.A. crooks、R. Sommerville
DOI:10.1002/jps.2600710306
日期:1982.3
Aromatic hydroxylated derivatives of spiro[indan-1,3'-pyrrolidine], designed as conformationally restricted analogs of profadol, were synthesized and pharmacologically evaluated in mice for analgesia and other central nervous system activities. None of the compounds synthesized were as potent as profadol in writhing and hot plate tests, but the 4-hydroxy derivative exhibited codeine-level analgesia
合成了螺环[茚满-1,3'-吡咯烷]的芳香族羟基化衍生物,设计为异丙酚的构象受限类似物,并在小鼠中进行了镇痛和其他中枢神经系统活动的药理学评估。在扭体试验和热板试验中,合成的化合物均不如普萘洛尔有效,但4-羟基衍生物在试验中表现出可待因水平的镇痛作用。