作者:Mosaad S. Mohamed、Rehab Kamel、Samar S. Fatahala
DOI:10.1016/j.ejmech.2011.04.034
日期:2011.7
The Pyrrole derivatives Ia–d were prepared and utilized for the preparation of pyrrolo[2,3-d]pyrimidine derivatives IIa–c, III, IVa–e, V and VIIIa–c; pyrrolo[3,2-e]tetrazolo[1,5-c]pyrimidine VI and pyrrolo[4,3e][1,2,4]triazolo[1,5-c]pyrimidine derivative derivatives VIIa–c. These some newly synthesized compounds were examined for their in vitro antimicrobial activity and in vivo anti-inflammatory.
制备了吡咯衍生物Ia-d,并用于制备吡咯并[2,3- d ]嘧啶衍生物IIa-c,III,IVa-e,V和VIIIa-c;吡咯并[3,2-e]四唑并[1,5-c]嘧啶VI和吡咯并[4,3e] [1,2,4]三唑并[1,5-c]嘧啶衍生物衍生物VIIa–c。检查了这些新合成的化合物的体外抗菌活性和体内活性消炎(药。结果表明,与布洛芬(标准消炎药)相比,这些化合物具有良好的消炎活性。本文还讨论了这些化合物的结构活性关系(SAR)和抗炎活性。