Synthesis, pharmacological evaluation and docking studies of new sulindac analogues
作者:Nelilma C. Romeiro、Ramon D.F. Leite、Lidia M. Lima、Suzana V.S. Cardozo、Ana L.P. de Miranda、Carlos A.M. Fraga、Eliezer J. Barreiro
DOI:10.1016/j.ejmech.2008.11.012
日期:2009.5
This paper describes the synthesis, pharmacological evaluation and docking studies of a series of new sulindac analogues. Overall, the designed compounds revealed good, in vivo, antinociceptive activity and satisfactory anti-inflammatory profile. Flexible molecular docking with COX-1/COX-2 has shown putative binding modes of the designed compounds while the theoretical evaluation of cell permeability based
本文描述了一系列新的舒林酸类似物的合成,药理学评价和对接研究。总体而言,设计的化合物显示出良好的体内抗伤害感受活性和令人满意的抗炎特性。与COX-1 / COX-2的灵活分子对接已显示出所设计化合物的推定结合模式,而基于Lipinski的5条法则对细胞通透性的理论评估有助于理化生物学结果。