Synthesis and Antiinflammatory Activity of Certain 5,6,7,8-Tetrahydroquinolines and Related Compounds
作者:William Calhoun、Richard P. Carlson、Roger Crossley、Louis J. Datko、Scott Dietrich、Kenneth Heatherington、Lisa A. Marshall、Peter J. Meade、Albert Opalko、Robin G. Shepherd
DOI:10.1021/jm00009a008
日期:1995.4
8-tetrahydroquinolines, which have good antiulcer activity, led to three distinct classes of compounds with good in vivo antiinflammatory activity. Initial efforts led to a series of alkenes derived from 5,6,7,8-tetrahydroquinolines substituted at the 8-position. A second approach concentrated on replacing the CH linkage of these 8-benzylidene-substituted compounds with other spacer groups and increasing the
具有良好抗溃疡活性的一些8-亚苄基-5,6,7,8-四氢喹啉的修饰导致具有良好体内抗炎活性的三类化合物。最初的努力导致了一系列衍生自在8位上取代的5,6,7,8-四氢喹啉的烯烃。第二种方法集中于用其他间隔基团取代这些8-亚苄基取代的化合物的CH键,并将环烷基环的尺寸从六元环增加到七元环,从而提供6,7,8,9-四氢-5H-环庚[b]吡啶类似物。最后,将取代基从环烷基环切换到吡啶环的2-位。还检查了2-取代基的变化。