Synthesis and biological evaluation of α,α-difluorobenzylphosphonic acid derivatives as small molecular inhibitors of protein-tyrosine phosphatase 1B
作者:Tsutomu Yokomatsu、Tetsuo Murano、Ikuko Umesue、Shinji Soeda、Hiroshi Shimeno、Shiroshi Shibuya
DOI:10.1016/s0960-894x(99)00027-x
日期:1999.2
series of alpha,alpha-difluorobenzylphosphonic acids having a hydrophobic functional group were prepared via the Stille coupling reaction from halogenated alpha,alpha-difluorobenzylphosphonates. Evaluation of inhibitory activity toward protein tyrosine phosphatase (PTP 1B) revealed that the ethynyl, phenylethynyl and (E)-styryl groups on the benzene nuclei increased the inhibitory activity of alpha,alph
通过Stille偶联反应,由卤化的α,α-二氟苄基膦酸酯制备了一系列具有疏水性官能团的α,α-二氟苄基膦酸。对蛋白酪氨酸磷酸酶(PTP 1B)的抑制活性的评估表明,苯核上的乙炔基,苯基乙炔基和(E)-苯乙烯基增加了α,α-二氟苄基膦酸的抑制活性。将(E)-苯乙烯基和双甲基磺酰胺官能团同时引入到α,α-二氟苄基膦酸的苯核上时,抑制活性显着提高。