In vivo formation of diazepam-like 1,4-benzodiazepines by Penicillium verrucosum var. verrucosum after administration of 2-aminobenzophenones and glycine.

G Bringmann, T Mader
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引用次数: 1

Abstract

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.

给药2-氨基苯甲酮和甘氨酸后,疣状青霉在体内形成类地西泮1,4-苯二氮卓类药物。
描述了由其假定的生物遗传前体2-氨基二苯甲酮和甘氨酸,由霉菌菌株疣状青霉菌在体内形成的类地西泮1,4-苯二氮卓类地氯硝地西泮。通过GC/MSD分析监测苯二氮卓的特征片段模式,确定了地氯诺地西泮的形成。通过d5 -2-氨基苯甲酮及其溴化和氯化衍生物对霉菌的投料实验,证实了去氯硝地西泮的鉴定。观察到1,4-苯二氮卓的形成取决于各种因素,如前体的施用时间、孵育时间和培养种类。这一结果代表了在活的有机体中从合理的生物合成前体中首次实际重新合成这种类地西泮1,4-苯二氮卓类药物,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-苯二氮卓类药物已在哺乳动物和植物组织中微量检测到。由于它们不同寻常的分子结构,它们以前被认为不适合任何传统的生物合成途径。
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