Bringmann G, Mader T
Institute of Organic Chemistry, University of Würzburg, Federal Republic of Germany.
J Neural Transm Gen Sect. 1995;101(1-3):169-81. doi: 10.1007/BF01271554.
The in vivo formation of the diazepam-like 1,4-benzodiazepine deschloronordiazepam from its assumed biogenetic precursors, 2-amino-benzophenone and glycine, by the mould strain Penicillium verrucosum var. verrucosum, is described. Deschloronordiazepam formation was established by GC/MSD analysis monitoring characteristic fragment patterns of the benzodiazepine moiety. The identification of deschloronordiazepam was confirmed by feeding experiments of D5-2-aminobenzophenone, as well as its brominated and chlorinated derivatives to the mould. The formation of the 1,4-benzodiazepine was observed to depend on various factors, e.g. the time of application of the precursors, duration of the incubation and kind of cultivation. The results represent the first actual de novo synthesis of such diazepam-like 1,4-benzodiazepines from plausible biosynthetic precursors in a living organism, in agreement with a biosynthetic concept recently established in our group. Such pharmacologically active 1,4-benzodiazepines had been detected in trace amounts in mammalian and plant tissues. Because of their unusual molecular framework, they had previously been considered not to fit into any conventional biosynthetic route.
描述了疣孢青霉变种从假定的生物合成前体2-氨基二苯甲酮和甘氨酸在体内形成地西泮样1,4-苯二氮䓬去氯甲基地西泮的过程。通过气相色谱/质谱检测分析监测苯二氮䓬部分的特征碎片模式来确定去氯甲基地西泮的形成。通过向霉菌投喂D5-2-氨基二苯甲酮及其溴化和氯化衍生物的实验,证实了去氯甲基地西泮的鉴定。观察到1,4-苯二氮䓬的形成取决于各种因素,例如前体的施用时间、培养持续时间和培养种类。这些结果代表了首次在活生物体中从合理的生物合成前体实际从头合成这种地西泮样1,4-苯二氮䓬,这与我们小组最近建立的生物合成概念一致。这种具有药理活性的1,4-苯二氮䓬已在哺乳动物和植物组织中检测到痕量。由于其不寻常的分子结构,它们以前被认为不适合任何传统的生物合成途径。