Dils W L, West T D, Walsh D A
J Biol Chem. 1977 Jun 25;252(12):4287-92.
The synthesis and properties of N6-monobutyryl adenosine 5'-monophosphate are described. The properties of synthesized monobutyryl nucleotide have been compared to those of a metabolite recognized in previous studies (Castagna, M. C., Palmer, W.K., and Walsh, D.A. (1977) Arch. Biochem. Biophys. 181, 46-60) as the major radioactive product produced in the liver upon perfusion with N6,O2'-dibutyryl cyclic [3H]adenosine 3':5'-monophosphate. By the criteria of cochromatography on DEAE-cellulose and in three thin layer chromatographic systems and from equivalent rates of alkaline hydrolysis, N6-monobutyryl adenosine 5'-monophosphate has been identified as a major hepatic metabolite of N6,O2'-dibutyryl cyclic adenosine 3':5'-monophosphate.
描述了N6 - 单丁酰腺苷5'-单磷酸的合成及性质。已将合成的单丁酰核苷酸的性质与先前研究(Castagna, M. C., Palmer, W.K., 和 Walsh, D.A. (1977) Arch. Biochem. Biophys. 181, 46 - 60)中所认可的一种代谢物的性质进行了比较,该代谢物是用N6,O2'-二丁酰环[3H]腺苷3':5'-单磷酸灌注肝脏时产生的主要放射性产物。根据在DEAE - 纤维素上的共色谱分析以及在三种薄层色谱系统中的分析标准,以及通过等效的碱性水解速率,N6 - 单丁酰腺苷5'-单磷酸已被鉴定为N6,O2'-二丁酰环腺苷3':5'-单磷酸的一种主要肝脏代谢物。