Massa S, Stefancich G, Artico M, Corelli F, Pantaleoni G C, Palumbo G, Fanini D, Giorgi R
Farmaco Sci. 1986 Apr;41(4):281-91.
The synthesis of new antiinflammatory aroylthiopheneacetic acids bearing a pyrrole moiety is described. These compounds can be regarded as analogues of thiaprofen and related isosteres. The antiinflammatory activity of the new pyrryl derivatives has been evaluated in comparison with indomethacin, tolmetin and the unknown 5-(2-chlorobenzoyl)thiophene-2-acetic acid. Among tested derivatives the compounds containing the pyrrole ring were devoid of analgesic-antiinflammatory activities.
描述了带有吡咯部分的新型抗炎芳酰基噻吩乙酸的合成。这些化合物可被视为噻洛芬及相关电子等排体的类似物。已将新型吡咯衍生物的抗炎活性与吲哚美辛、托美丁和未知的5-(2-氯苯甲酰基)噻吩-2-乙酸进行了比较评估。在所测试的衍生物中,含有吡咯环的化合物没有镇痛抗炎活性。