Literature DB >> 17343885

Chemistry and pharmacology of oxyprenylated secondary plant metabolites.

Francesco Epifano1, Salvatore Genovese, Luigi Menghini, Massimo Curini.   

Abstract

Oxyprenylated natural products (isopentenyloxy-, geranyloxy- and the less spread farnesyloxy- compounds and their biosynthetic derivatives) represent a family of secondary metabolites that have been considered for years just as biosynthetic intermediates of C-prenylated derivatives. Only in the last decade these natural products have been recognized as interesting and valuable biologically active phytochemicals. Up to now about 300 molecules have been isolated from plants mainly belonging to the families of Rutaceae and Compositae, comprising common edible vegetables and fruits. A wide variety of compounds containing a prenyloxy side chain have been isolated and these comprise alkaloids, coumarins, flavonoids, cinnamic acids, benzoic acids, phenols, alcohols, aldehydes, anthraquinones, chalcones, lignans, xanthones, aceto- and benzophenones and other more uncommon skeletons. Many of the isolated oxyprenylated natural products and their semisynthetic derivatives were shown to exert in vitro and in vivo remarkable anti-cancer, anti-inflammatory, anti-microbial and anti-fungal effects. The aim of this review is to examine in detail the different types of oxyprenylated natural compounds from a phytochemical and pharmacological point of view.

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Year:  2007        PMID: 17343885     DOI: 10.1016/j.phytochem.2007.01.019

Source DB:  PubMed          Journal:  Phytochemistry        ISSN: 0031-9422            Impact factor:   4.072


  16 in total

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2.  Analysis of biologically active oxyprenylated ferulic acid derivatives in Citrus fruits.

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9.  The cytotoxic activities of 7-isopentenyloxycoumarin on 5637 cells via induction of apoptosis and cell cycle arrest in G2/M stage.

Authors:  Fereshteh Haghighi; Maryam M Matin; Ahmad Reza Bahrami; Mehrdad Iranshahi; Fatemeh B Rassouli; Azadeh Haghighitalab
Journal:  Daru       Date:  2014-01-06       Impact factor: 3.117

10.  Facile and promising method for michael addition of indole and pyrrole to electron-deficient trans-β-nitroolefins catalyzed by a hydrogen bond donor catalyst Feist's acid and preliminary study of antimicrobial activity.

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Journal:  ScientificWorldJournal       Date:  2014-01-16
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