Burnelli S, Varoli L, Guarnieri A, Lumachi B
Dipartimento di Scienze Farmaceutiche, Università degli Studi di Bologna.
Boll Chim Farm. 1991 Apr;130(4):133-5.
As fluorenyl rigid analogues of previous biphenylyl alcanoic acids with very interesting antiinflammatory activity, the 3-(m-tolyl and m-anisyl)-3-hydroxy-3-(2-fluorenyl)-propionic acids have been prepared by means of the Reformatsky reaction and following hydrolysis of the obtained ethyl esters. The preliminary antiinflammatory assay showed that the structural modification inactivates the compounds.
作为先前具有非常有趣抗炎活性的联苯基链烷酸的芴基刚性类似物,3-(间甲苯基和间甲氧基苯基)-3-羟基-3-(2-芴基)丙酸已通过Reformatsky反应并在所得乙酯水解后制备。初步抗炎试验表明,结构修饰使这些化合物失活。