McClard R W, Tsimikas S, Schriver K E
Arch Biochem Biophys. 1986 Feb 15;245(1):282-6. doi: 10.1016/0003-9861(86)90215-8.
We describe the synthesis of a mixture of D-manno- and D-gluco-2,5-anhydro-1-deoxy-1-phosphonohexitol 6-phosphate via a Horner-Emmons reaction of 2,3,5-tri-O-benzyl-beta-D-arabinofuranose followed by phosphorylation of the equivalent 6-position and subsequent deprotection. This mixture inhibits fructose-1,6-bisphosphatase; the concentration required for half-maximal effect in the presence of 25 microM AMP is approximately 6 microM. The mixture of analogs also stimulates 6-phosphofructo-1-kinase from rabbit liver; the concentration required to reach one-half Vmax was found to be ca. 25 microM at 0.25 mM fructose 6-phosphate and 50 microM AMP. These analogs have replaced the labile anomeric phosphate of fructose 2,6-bisphosphate with a stable methylenephosphonate, and could be of great interest due to their appropriate physiological effects and their chemical stability.
我们描述了通过2,3,5-三-O-苄基-β-D-阿拉伯呋喃糖的霍纳-埃蒙斯反应,接着对相应的6-位进行磷酸化以及随后的脱保护反应,合成D-甘露糖型和D-葡萄糖型2,5-脱水-1-脱氧-1-膦酰基己糖醇6-磷酸酯混合物的过程。该混合物可抑制果糖-1,6-二磷酸酶;在25μM AMP存在下产生半数最大效应所需的浓度约为6μM。该类似物混合物还能刺激兔肝中的6-磷酸果糖-1-激酶;在0.25 mM果糖6-磷酸和50μM AMP条件下,达到最大反应速度一半时所需的浓度约为25μM。这些类似物用稳定的亚甲基膦酸酯取代了果糖2,6-二磷酸不稳定的异头磷酸酯,鉴于其适当的生理效应和化学稳定性,可能具有极大的研究价值。