Westerduin P, Willems H A, van Boeckel C A
Akzo Pharma, Organon Scientific Development Group, Oss, Netherlands.
Carbohydr Res. 1992 Oct 9;234:131-40. doi: 10.1016/0008-6215(92)85044-z.
The syntheses are described of four isosteric racemic myo-inositol 1,4,5-trisphosphate (1) analogues with the phosphate groups replaced by sulfonamide (2), sulfate (3), methylphosphonate (4), and carboxymethyl (5). None of these compounds had any affinity for the IP3 receptor or induced platelet aggregation.
描述了四种等排体的外消旋肌醇1,4,5 -三磷酸酯(1)类似物的合成,其中磷酸基团被磺酰胺(2)、硫酸酯(3)、甲基膦酸酯(4)和羧甲基(5)取代。这些化合物均对IP3受体没有任何亲和力,也不会诱导血小板聚集。