作者:Wen-Shyong Li、James D. McChesney
DOI:10.1002/jps.2600810711
日期:1992.7
ehydroabietate (29), 16-nor-16-carboxydehydroabietic acid (30), 16-nor-16-carboxydehydroabietinol (31), 7-keto-16-nor-16-carboxydehydroabietic acid (32), methyl 7-hydroxy-16-nor-16-carboxydehydroabietate (33), and 7-hydroxy-16-nor-16-carboxydehydroabietic acid (34) were prepared from dehydroabietic acid. Only 22 and 32 had weak anti-inflammatory activity.
16-nor-16-羧基脱氢松香酸甲酯(22),16-nor-16-羧基脱氢松香醇乙酸酯(23),7-酮16-nor-16-nor-16-羧基脱氢松香酸甲酯(29),16-nor-16-羧基脱氢松香酸(30) ),16-nor-16-羧基脱氢松香醇(31),7-酮-16-nor-16-羧基脱氢松香酸(32),7-羟基-16-nor-16-羧基脱氢松香酸甲酯(33)和7-羟基-由脱氢松香酸制备16-nor-16-羧基脱氢松香酸(34)。只有22和32的抗炎活性较弱。