RSC - Nat. Prod. Rep. latest articles RSC - Nat. Prod. Rep. latest articles http://xlink.rsc.org/jumptojournal.cfm?journal_code=NP The Royal Society of Chemistry en-gb Copyright (c) 2010 The Royal Society of Chemistry Nat. Prod. Rep. Copyright (c) The Royal Society of Chemistry contracts-copyright@rsc.org 0265-05681460-4752The Royal Society of Chemistry The Royal Society of Chemistry Royal Society of Chemistry - Nat. Prod. Rep. latest articles RSC - Nat. Prod. Rep. latest articles http://www.rsc.org text/html text Prenylated indole derivatives from fungi: structure diversity, biological activities, biosynthesis and chemoenzymatic synthesis http://xlink.rsc.org/?DOI=b909987p&RSS=1 Prenylated indole alkaloids are a large group of hybrid natural products mainly found in filamentous fungi. This article describes their structure diversity and biological activities, as well as the progress on their biosynthesis and production by using overproduced and purified enzymes.<p><img align="center" src="http://www.rsc.org/ejga/NP/2010/b909987p-ga.gif"/> </p>Shu-Ming Li <br/> (Review from Nat. Prod. Rep.)<br/> Shu-Ming Li, Nat. Prod. Rep., 2010, DOI: 10.1039/b909987p<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry Prenylated indole derivatives from fungi: structure diversity, biological activities, biosynthesis and chemoenzymatic synthesis Shu-Ming Li 10.1039/b909987p Nat. Prod. Rep., 2010, DOI: 10.1039/b909987p html/pdf 2009-11-19 The Royal Society of Chemistry Copyright (c) 2010 The Royal Society of Chemistry DOI 10.1039/b909987p Biosynthesis and biomimetic synthesis of alkaloids isolated from plants of the Nitraria and Myrioneuron genera: an unusual lysine-based metabolism http://xlink.rsc.org/?DOI=b911866g&RSS=1 This review describes a wide panel of alkaloids isolated from plants of the Nitraria genus, focusing on their biosynthesis and discussing the resulting biomimetic chemistry in relevant cases.<p><img align="center" src="http://www.rsc.org/ejga/NP/2010/b911866g-ga.gif"/> </p>Edmond Gravel, Erwan Poupon <br/> (Review from Nat. Prod. Rep.)<br/> Edmond Gravel, Nat. Prod. Rep., 2010, DOI: 10.1039/b911866g<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry Biosynthesis and biomimetic synthesis of alkaloids isolated from plants of the Nitraria and Myrioneuron genera: an unusual lysine-based metabolism Edmond Gravel Erwan Poupon 10.1039/b911866g Nat. Prod. Rep., 2010, DOI: 10.1039/b911866g html/pdf 2009-11-17 The Royal Society of Chemistry Copyright (c) 2010 The Royal Society of Chemistry DOI 10.1039/b911866g Imaging mass spectrometry of natural products http://xlink.rsc.org/?DOI=b915674g&RSS=1 This Highlight article describes three different imaging mass spectrometry (IMS) approaches, MALDI, DESI and SIMS and their recent applications in the analysis of natural products. IMS has opened up a new avenue for establishing the functional roles of natural products.<p><img align="center" src="http://www.rsc.org/ejga/NP/2009/b915674g-ga.gif"/> </p>Eduardo Esquenazi, Yu-Liang Yang, Jeramie Watrous, William H. Gerwick, Pieter C. Dorrestein <br/> (Highlight from Nat. Prod. Rep.)<br/> Eduardo Esquenazi, Nat. Prod. Rep., 2009, DOI: 10.1039/b915674g<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry Imaging mass spectrometry of natural products Eduardo Esquenazi Yu-Liang Yang Jeramie Watrous William H. Gerwick Pieter C. Dorrestein 10.1039/b915674g Nat. Prod. Rep., 2009, DOI: 10.1039/b915674g html/pdf 2009-11-09 The Royal Society of Chemistry Copyright (c) 2010 The Royal Society of Chemistry DOI 10.1039/b915674g Hot off the press http://xlink.rsc.org/?DOI=b921623p&RSS=1 A personal selection of 30 recent papers is presented covering various aspects of current developments in bioorganic chemistry and novel natural products such as the tetrameric polysulfur dopamine-derived alkaloid lissoclibadin 8 from the ascidian Lissoclinum cf. badium.<p><img align="center" src="http://www.rsc.org/ejga/NP/2009/b921623p-ga.gif"/> </p>Robert A. Hill, Andrew Sutherland <br/> (Hot off the Press Article from Nat. Prod. Rep.)<br/> Robert A. Hill, Nat. Prod. Rep., 2009, DOI: 10.1039/b921623p<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry Hot off the press Robert A. Hill Andrew Sutherland 10.1039/b921623p Nat. Prod. Rep., 2009, DOI: 10.1039/b921623p html/pdf 2009-11-03 The Royal Society of Chemistry Copyright (c) 2010 The Royal Society of Chemistry DOI 10.1039/b921623p Epigenome manipulation as a pathway to new natural product scaffolds and their congeners http://xlink.rsc.org/?DOI=b920860g&RSS=1 This Highlight discusses both chemical and molecular methods for manipulating the fungal epigenome, which are providing unique opportunities for probing the chemical diversity of silent biosynthetic pathways in fungi.<p><img align="center" src="http://www.rsc.org/ejga/NP/2010/b920860g-ga.gif"/> </p>Robert H. Cichewicz <br/> (Highlight from Nat. Prod. Rep.)<br/> Robert H. Cichewicz, Nat. Prod. Rep., 2010, DOI: 10.1039/b920860g<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry Epigenome manipulation as a pathway to new natural product scaffolds and their congeners Robert H. Cichewicz 10.1039/b920860g Nat. Prod. Rep., 2010, DOI: 10.1039/b920860g html/pdf 2009-10-27 The Royal Society of Chemistry Copyright (c) 2010 The Royal Society of Chemistry DOI 10.1039/b920860g New therapeutic potential for psychoactive natural products http://xlink.rsc.org/?DOI=b912196j&RSS=1 This Highlight describes the history of investigations into several classes of mind-altering natural products and relates recent and potential therapeutic uses for these agents.<p><img align="center" src="http://www.rsc.org/ejga/NP/2010/b912196j-ga.gif"/> </p>Katherine M. Prevatt-Smith, Thomas E. Prisinzano <br/> (Highlight from Nat. Prod. Rep.)<br/> Katherine M. Prevatt-Smith, Nat. Prod. Rep., 2010, DOI: 10.1039/b912196j<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry New therapeutic potential for psychoactive natural products Katherine M. Prevatt-Smith Thomas E. Prisinzano 10.1039/b912196j Nat. Prod. Rep., 2010, DOI: 10.1039/b912196j html/pdf 2009-10-26 The Royal Society of Chemistry Copyright (c) 2010 The Royal Society of Chemistry DOI 10.1039/b912196j