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植物科血皮草科来源的苯并菲咯酮类化合物的分布、生物合成和生物活性。

Distribution, biosynthesis, and biological activity of phenylphenalenone-type compounds derived from the family of plants, Haemodoraceae.

机构信息

School of Science (Applied Chemistry and Environmental Science), RMIT University, GPO Box 2476, Melbourne, Victoria 3001, Australia.

出版信息

Nat Prod Rep. 2019 May 22;36(5):753-768. doi: 10.1039/c8np00067k.

Abstract

Covering: up to 2018 The Haemodoraceae family is a monocotyledonous family in the order Commelinales consisting of 14 genera. Many species from the family are endemic to Australia and their use by the Aboriginal People of Australia as both pigments or remedies has been ethnobotanically documented. Phenylphenalenones are phenolic specialised metabolites consisting of a tricyclic phenalene nucleus with a ketone moiety and a lateral phenyl ring. Depending on their structural variance, four classes can be distinguished including the phenylphenalenones, oxabenzochrysenones, phenylbenzoisochromenones and phenylbenzoisoquinolinediones. The phenylphenalenone class has become the order's chemotaxonomic marker with a documented range of biological activities. This biological activity arises from the phototoxic properties of their ring system, a phenomenon most comprehensively observed amongst a widely cultivated family of the Commelinales order, Musaceae (banana). Within the family Haemodoraceae, the formation of the phenylphenalenone-class phytoanticipins is an intrinsic function of their growth, whereas within the family Musaceae these compounds are formed as phytoalexins in response to pathogenic attack or stress. The compounds produced within these two families differ in their substitution, with Musaceae-derived phytoalexins tending to be the more phototoxic 4-phenylphenalenones and the Haemodoraceae-derived phytoanticipins being of the more inert 9-phenylphenalenone type structure. Various other substitution patterns have been documented across the class, yet their biosynthetic mechanism is consistent, proceeding from simple phenylpropanoids through a diarylheptanoid intermediate, which cyclises to form the phenylphenalenone nucleus. Phenylphenalenone-related compounds have also been observed within the fungal kingdom, yet their biosynthetic route is based upon an alternative polymalonate pathway. This review focuses on Haemodoraceae-derived phenylphenalenone-type compounds, their distribution amongst species, throughout the plant organism, their biological activity and their biosynthesis.

摘要

涵盖范围

截至 2018 年,葱叶科是单子叶植物葱目下的一科,包含 14 个属。该科的许多物种都是澳大利亚特有的,其被澳大利亚原住民用作颜料或药物已在民族植物学上有记载。苯并菲酚类化合物是由三环菲核、酮部分和侧苯基环组成的酚类特殊代谢物。根据其结构差异,可分为四类,包括苯并菲酚类、氧杂苯并色烯酮类、苯并异苯并色烯酮类和苯并异喹啉二酮类。苯并菲酚类化合物已成为该目系统化学分类的标志物,并具有广泛的生物活性。这种生物活性源于其环系统的光毒性特性,这种现象在 Commelinales 目广泛栽培的一科,Musaceae(香蕉)中观察到的最为全面。在葱叶科中,苯并菲酚类植物抗毒素的形成是其生长的固有功能,而在 Musaceae 科中,这些化合物是作为植物抗毒素在受到病原攻击或胁迫时形成的。这两个科产生的化合物在取代上有所不同,Musaceae 衍生的植物抗毒素往往是更具光毒性的 4-苯并菲酚类化合物,而葱叶科衍生的植物抗毒素则是更为惰性的 9-苯并菲酚类化合物结构。在整个类群中还记录了各种其他取代模式,但它们的生物合成机制是一致的,从简单的苯基丙氨酸通过二芳基庚烷中间体进行,该中间体环化形成苯并菲酚核。在真菌王国也观察到了与苯并菲酚相关的化合物,但它们的生物合成途径是基于替代的聚丙二酸盐途径。本综述重点介绍了葱叶科衍生的苯并菲酚类化合物,它们在物种中的分布,在整个植物体内的分布,它们的生物活性和生物合成。

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