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Synthesis of a 2,4,6,8,10-dodecapentanoic acid thioester as a substrate for biosynthesis of heat stable antifungal factor (HSAF)

机译:2,4,6,8,10-十二烷酸的合成 硫酯作为生物合成热的基质 稳定的抗真菌因子(HsaF)

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摘要

The N-acetylcystamine (SNAC) thioester of dodecapentaenoic acid, an analog of a putative intermediate in the biosynthesis of Heat Stable Antifungal Factor (HSAF), is synthesized. Key steps include sequential Horner–Emmons homologations with the Weinreb amide of diethylphosponoacetic acid, and thioesterification of an aldol-derived 3-hydroxyalkanoate, which serves as a stable precursor of the sensitive polyenoate. The thioester was investigated as a biosynthetic substrate using a purified nonribosomal peptide synthetase and was not incorporated in the observed products.
机译:合成了十二碳五烯酸的N-乙酰半胱胺(SNAC)硫酯,它是热稳定抗真菌因子(HSAF)生物合成中假定的中间体的类似物。关键步骤包括与二乙基膦酸乙酸的Weinreb酰胺进行连续的霍纳-埃蒙斯同源性,以及醛醇衍生的3-羟基链烷酸酯的硫酯化,后者用作敏感多烯酸酯的稳定前体。使用纯化的非核糖体肽合成酶对硫酯作为生物合成底物进行了研究,未将其掺入观察到的产物中。

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