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        <title>RSC - Nat. Prod. Rep. latest articles via MedWorm.com</title>
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        <lastBuildDate>Thu, 09 Feb 2012 13:01:56 +0100</lastBuildDate>
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            <title>Electrophilic and nucleophilic enzymatic cascade reactions in biosynthesis</title>
            <link>http://www.medworm.com/index.php?rid=5673437&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2F7Pl_2bDQdgU%2FC2NP00078D</link>
            <description>Nat. Prod. Rep., 2012, Advance ArticleDOI: 10.1039/C2NP00078D, ReviewBarbara T. Ueberbacher, Melanie Hall, Kurt FaberCyclic terpenoids and polyethers are formed via enzyme-initiated cascade reactions for ring formation, which proceed either via electrophilic (cationic) or nucleophilic (anionic) pathways through (i) triggering of the cascade ('initiation'), (ii) 'proliferation' of the cyclization and (iii) 'termination' of the cascade.To cite this article before page numbers are assigned, use the DOI form of citation above.The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
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            <pubDate>Thu, 09 Feb 2012 17:44:30 +0100</pubDate>
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            <title>Triptolide: structural modifications, structure-activity relationships, bioactivities, clinical development and mechanisms</title>
            <link>http://www.medworm.com/index.php?rid=5624309&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2FikU3aVm-2Rg%2FC2NP00088A</link>
            <description>Nat. Prod. Rep., 2012, Advance ArticleDOI: 10.1039/C2NP00088A, ReviewZhao-Li Zhou, Ya-Xi Yang, Jian Ding, Yuan-Chao Li, Ze-Hong MiaoThis review covers research efforts of the last forty years, focusing on the structural modifications, structure-activity relationships, pharmacology and clinical development of triptolide, a principal bioactive ingredient of Tripterygium wilfordii Hook F.To cite this article before page numbers are assigned, use the DOI form of citation above.The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
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            <pubDate>Tue, 24 Jan 2012 18:17:14 +0100</pubDate>
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            <title>Didemnins, tamandarins and related natural products</title>
            <link>http://www.medworm.com/index.php?rid=5624308&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2F3ZjaUOQAvzc%2FC2NP00065B</link>
            <description>Nat. Prod. Rep., 2012, Advance ArticleDOI: 10.1039/C2NP00065B, ReviewJisun Lee, Judith N. Currano, Patrick J. Carroll, Madeleine M. JoullieThis review highlights the long-standing study of didemnins and its critical application towards the understanding of the molecular mechanism of action of tamandarins and their potential use as therapeutic agents.To cite this article before page numbers are assigned, use the DOI form of citation above.The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
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            <pubDate>Tue, 24 Jan 2012 18:17:14 +0100</pubDate>
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            <title>The taxonomy, biology and chemistry of the fungal Pestalotiopsis genus</title>
            <link>http://www.medworm.com/index.php?rid=5603408&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2FcxlEAofAIv4%2FC2NP00073C</link>
            <description>Nat. Prod. Rep., 2012, Advance ArticleDOI: 10.1039/C2NP00073C, ReviewXiao-Long Yang, Jing-Ze Zhang, Du-Qiang LuoA growing body of evidence indicates that the Pestalotiopsis genus represents a huge and largely untapped resource of bioactive metabolites. This review systematically surveys the taxonomy, biology and chemistry of the Pestalotiopsis genus. It also summarises the biosynthetic relationships and chemical synthesis of secondary metabolites.To cite this article before page numbers are assigned, use the DOI form of citation above.The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
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            <pubDate>Wed, 18 Jan 2012 18:44:08 +0100</pubDate>
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            <title>Natural products as kinase inhibitors</title>
            <link>http://www.medworm.com/index.php?rid=5592144&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2FnH0JhKdAt-Y%2FC2NP00097K</link>
            <description>Nat. Prod. Rep., 2012, Advance ArticleDOI: 10.1039/C2NP00097K, ReviewJing Liu, Yi Hu, David L. Waller, Junfeng Wang, Qingsong LiuThis review discusses the history of several classes of natural products as kinase inhibitors, analyzes their structural binding information and highlights their therapeutic development potential.To cite this article before page numbers are assigned, use the DOI form of citation above.The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
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            <pubDate>Sun, 15 Jan 2012 07:03:24 +0100</pubDate>
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            <title>The chemical ecology of cyanobacteria</title>
            <link>http://www.medworm.com/index.php?rid=5592143&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2FuxmMU6Lalec%2FC2NP00075J</link>
            <description>Nat. Prod. Rep., 2012, Advance ArticleDOI: 10.1039/C2NP00075J, ReviewPedro N. Leao, Niclas Engene, Agostinho Antunes, William H. Gerwick, Vitor VasconcelosCyanobacteria are ancient photoautotrophic prokaryotes that have adapted to a wide range of habitats and display a high degree of chemical and biological diversity. This review describes current knowledge regarding the chemically mediated ecology of these organisms.To cite this article before page numbers are assigned, use the DOI form of citation above.The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
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            <pubDate>Sun, 15 Jan 2012 07:03:24 +0100</pubDate>
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            <title>Hot off the press</title>
            <link>http://www.medworm.com/index.php?rid=5568199&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2FaWVXO_D4UW8%2FC1NP90052H</link>
            <description>Nat. Prod. Rep., 2012, Advance ArticleDOI: 10.1039/C1NP90052H, Hot off the Press ArticleRobert A. Hill, Andrew SutherlandA personal selection of 32 recent papers is presented covering various aspects of current developments in bioorganic chemistry and novel natural products such as psychotripine from leaves of Psychotria pilifera.To cite this article before page numbers are assigned, use the DOI form of citation above.The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
            <author>RSC - Nat. Prod. Rep. latest articles</author>
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            <pubDate>Sat, 07 Jan 2012 00:11:56 +0100</pubDate>
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            <title>Advances in Aspergillus secondary metabolite research in the post-genomic era</title>
            <link>http://www.medworm.com/index.php?rid=5568198&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2FEe1rZARX0UE%2FC2NP00084A</link>
            <description>Nat. Prod. Rep., 2012, Advance ArticleDOI: 10.1039/C2NP00084A, ReviewJames F. Sanchez, Amber D. Somoza, Nancy P. Keller, Clay C. C. WangThe genomic sequence data from several Aspergillus species has proven to be a boon to researchers interested in studying the genetics and biochemistry underlying secondary metabolism in this important fungal genus.To cite this article before page numbers are assigned, use the DOI form of citation above.The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
            <author>RSC - Nat. Prod. Rep. latest articles</author>
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            <pubDate>Sat, 07 Jan 2012 00:11:56 +0100</pubDate>
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            <title>Natural product DNA major groove binders</title>
            <link>http://www.medworm.com/index.php?rid=5532524&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2FYCfW1oLMYK8%2FC1NP00054C</link>
            <description>Nat. Prod. Rep., 2012, Advance ArticleDOI: 10.1039/C1NP00054C, HighlightParis L. Hamilton, Dev P. AryaPreviously known natural products known to possess elements of DNA major groove binding do so with assistance from other modes of DNA binding, such as intercalation or minor groove interactions. Recent reports of non-covalent major groove binding with aminoglycosides have revealed them as promising leads for DNA major groove binding probes or drugs.To cite this article before page numbers are assigned, use the DOI form of citation above.The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
            <author>RSC - Nat. Prod. Rep. latest articles</author>
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            <pubDate>Fri, 23 Dec 2011 06:51:17 +0100</pubDate>
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            <title>Angucyclines: Biosynthesis, mode-of-action, new natural products, and synthesis</title>
            <link>http://www.medworm.com/index.php?rid=5532523&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2FfaYSzM3GySw%2FC1NP00068C</link>
            <description>Nat. Prod. Rep., 2012, Advance ArticleDOI: 10.1039/C1NP00068C, ReviewMadan K. Kharel, Pallab Pahari, Micah D. Shepherd, Nidhi Tibrewal, S. Eric Nybo, Khaled A. Shaaban, Jurgen RohrThe angucycline group is the largest group of type II PKS-engineered natural products, rich in biological activities and chemical scaffolds. This stimulated synthetic creativity and biosynthetic investigations focusing on oxidative rearrangement processes and unusual tailoring enzymes.To cite this article before page numbers are assigned, use the DOI form of citation above.The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
            <author>RSC - Nat. Prod. Rep. latest articles</author>
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            <pubDate>Fri, 23 Dec 2011 06:51:17 +0100</pubDate>
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            <title>Marine natural products</title>
            <link>http://www.medworm.com/index.php?rid=5532522&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2FOu09v3b2sMQ%2FC2NP00090C</link>
            <description>Nat. Prod. Rep., 2012, Advance ArticleDOI: 10.1039/C2NP00090C, ReviewJohn W. Blunt, Brent R. Copp, Robert A. Keyzers, Murray H. G. Munro, Michele R. PrinsepThis 2010 review of marine natural products describes 1003 new compounds and reports structural revisions and assignments of absolute configurations for previously described compounds. Included is the final resolution of the palau'amine saga with assignment of absolute configuration and total synthesis.To cite this article before page numbers are assigned, use the DOI form of citation above.The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
            <author>RSC - Nat. Prod. Rep. latest articles</author>
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            <pubDate>Fri, 23 Dec 2011 06:51:17 +0100</pubDate>
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            <title>Biosynthesis of 3,5-AHBA-derived natural products</title>
            <link>http://www.medworm.com/index.php?rid=5532521&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2FhUt1uUz4LeE%2FC2NP00019A</link>
            <description>Nat. Prod. Rep., 2012, Advance ArticleDOI: 10.1039/C2NP00019A, ReviewQianjin Kang, Yuemao Shen, Linquan BaiThis review covers the biosynthesis of 3-amino-5-hydroxybenzoic acid (3,5-AHBA, AHBA)-derived natural products from a molecular genetics, chemical and biochemical perspective.To cite this article before page numbers are assigned, use the DOI form of citation above.The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
            <author>RSC - Nat. Prod. Rep. latest articles</author>
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            <pubDate>Fri, 23 Dec 2011 06:51:17 +0100</pubDate>
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            <title>Beyond ethylmalonyl-CoA: The functional role of crotonyl-CoA carboxylase/reductase homologs in expanding polyketide diversity</title>
            <link>http://www.medworm.com/index.php?rid=5464653&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2FQoJtpmdTYHQ%2FC1NP00082A</link>
            <description>Nat. Prod. Rep., 2012, Advance ArticleDOI: 10.1039/C1NP00082A, ReviewMicheal C. Wilson, Bradley S. MooreThis review covers the emerging biosynthetic role of crotonyl-CoA carboxylase/reductase (CCR) homologs in extending the structural and functional diversity of polyketide natural products.To cite this article before page numbers are assigned, use the DOI form of citation above.The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
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            <pubDate>Fri, 02 Dec 2011 07:04:38 +0100</pubDate>
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            <title>Happy New Year from Natural Product Reports</title>
            <link>http://www.medworm.com/index.php?rid=5464652&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2FCthoVxW7C0I%2FC1NP90048J</link>
            <description>Nat. Prod. Rep., 2012, Advance ArticleDOI: 10.1039/C1NP90048J, EditorialAs NPR enters its 29th year of publication we look back on another successful year for the journal.To cite this article before page numbers are assigned, use the DOI form of citation above.The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
            <author>RSC - Nat. Prod. Rep. latest articles</author>
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            <pubDate>Fri, 02 Dec 2011 07:04:38 +0100</pubDate>
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            <title>Macrocylic bisbibenzyl natural products and their chemical synthesis</title>
            <link>http://www.medworm.com/index.php?rid=5427680&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2F0llyNFbSy4U%2FC1NP00080B</link>
            <description>Nat. Prod. Rep., 2012, Advance ArticleDOI: 10.1039/C1NP00080B, ReviewDavid C. Harrowven, Sarah L. KostiukThe review focuses on new additions to the macrocyclic bisbibenzyl family of natural products; the strategies used to effect their synthesis and some stereochemical considerations. It provides a timely update to a Natural Product Reports article by Keseru and Nogradi (Nat. Prod. Rep. 1995, 12, 69-75).To cite this article before page numbers are assigned, use the DOI form of citation above.The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
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            <pubDate>Sun, 20 Nov 2011 06:25:54 +0100</pubDate>
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            <title>Aminobenzoates as building blocks for natural product assembly lines</title>
            <link>http://www.medworm.com/index.php?rid=5404456&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2Frufiv3C0SJU%2FC1NP00072A</link>
            <description>Nat. Prod. Rep., 2012, Advance ArticleDOI: 10.1039/C1NP00072A, ReviewChristopher T. Walsh, Stuart W. Haynes, Brian D. AmesAminobenzoates, derived from chorismate and aminoshikimate intermediates, feature heavily in primary and secondary metabolism: forming key components of folate and tryptophan scaffolds and being incorporated into a diverse group of cyclic secondary metabolites.To cite this article before page numbers are assigned, use the DOI form of citation above.The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
            <author>RSC - Nat. Prod. Rep. latest articles</author>
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            <pubDate>Mon, 14 Nov 2011 05:28:16 +0100</pubDate>
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            <title>Sesquiterpene synthases: Passive catalysts or active players?</title>
            <link>http://www.medworm.com/index.php?rid=5404455&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2FxVlUWjYs_TY%2FC1NP00060H</link>
            <description>Nat. Prod. Rep., 2012, Advance ArticleDOI: 10.1039/C1NP00060H, ReviewDavid J. Miller, Rudolf K. AllemannSesquiterpene synthases catalyse turnover of farnesyl diphosphate to generate natural products of an enormous diversity in structure, stereochemistry, biological function and application. Recent research suggests that these enzymes play multifaceted active roles in what are arguably the most complex biosynthetic reactions.To cite this article before page numbers are assigned, use the DOI form of citation above.The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
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            <pubDate>Mon, 14 Nov 2011 05:28:16 +0100</pubDate>
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            <title>Influenza neuraminidase: A druggable target for natural products</title>
            <link>http://www.medworm.com/index.php?rid=5374226&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2FmV2z8-EQY9M%2FC1NP00053E</link>
            <description>Nat. Prod. Rep., 2011, Advance ArticleDOI: 10.1039/C1NP00053E, ReviewUlrike Grienke, Michaela Schmidtke, Susanne von Grafenstein, Johannes Kirchmair, Klaus R. Liedl, Judith M. RollingerThis review covers the increasing research efforts of the past decade, focusing on the structure, function and druggability of influenza NA, and its inhibition by natural products. Latest developments in theoretical and experimental research on NA for lead discovery strategies from nature are presented.To cite this article before page numbers are assigned, use the DOI form of citation above.The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
            <author>RSC - Nat. Prod. Rep. latest articles</author>
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            <pubDate>Fri, 04 Nov 2011 16:46:43 +0100</pubDate>
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            <title>The diazofluorene antitumor antibiotics: Structural elucidation, biosynthetic, synthetic, and chemical biological studies</title>
            <link>http://www.medworm.com/index.php?rid=5374225&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2FLsXjE_yJgfE%2FC1NP00052G</link>
            <description>Nat. Prod. Rep., 2011, Advance ArticleDOI: 10.1039/C1NP00052G, ReviewSeth B. Herzon, Christina M. WooThe kinamycins and lomaiviticins are cytotoxic bacterial metabolites that possess a diazo substituent embedded in a highly oxidized carbocyclic framework (diazofluorene). This review summarizes their isolation, structural elucidation, and biosynthesis, synthetic studies in this area, and chemical biological investigations.To cite this article before page numbers are assigned, use the DOI form of citation above.The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
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            <pubDate>Fri, 04 Nov 2011 16:46:43 +0100</pubDate>
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            <title>Hot off the press</title>
            <link>http://www.medworm.com/index.php?rid=5354736&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2FKcHOs3eLN2s%2FC1NP90043A</link>
            <description>Nat. Prod. Rep., 2011, Advance ArticleDOI: 10.1039/C1NP90043A, Hot off the Press ArticleRobert A. Hill, Andrew SutherlandA personal selection of 31 recent papers is presented covering various aspects of current developments in bioorganic chemistry and novel natural products, such as paracaseolide A from Sonneratia paracaseolaris.To cite this article before page numbers are assigned, use the DOI form of citation above.The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
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            <pubDate>Thu, 27 Oct 2011 22:59:31 +0100</pubDate>
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        <item>
            <title>Isoprenoids in three-dimensional space: the stereochemistry of terpene biosynthesis</title>
            <link>http://www.medworm.com/index.php?rid=5301471&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2FDL6l7TV7Qho%2FC1NP00063B</link>
            <description>Nat. Prod. Rep., 2011, Advance ArticleDOI: 10.1039/C1NP00063B, ReviewJeroen S. DickschatThis review covers for the first time all stereochemical aspects of the biosynthetic pathways to terpenes.To cite this article before page numbers are assigned, use the DOI form of citation above.The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
            <author>RSC - Nat. Prod. Rep. latest articles</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5301471</comments>
            <pubDate>Mon, 10 Oct 2011 06:12:11 +0100</pubDate>
            <guid isPermaLink="false">5301471</guid>        </item>
        <item>
            <title>Multitargeting by curcumin as revealed by molecular interaction studies</title>
            <link>http://www.medworm.com/index.php?rid=5292336&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2FHfRjtX-DiNs%2FC1NP00051A</link>
            <description>Nat. Prod. Rep., 2011, Advance ArticleDOI: 10.1039/C1NP00051A, ReviewSubash C. Gupta, Sahdeo Prasad, Ji Hye Kim, Sridevi Patchva, Lauren J. Webb, Indira K. Priyadarsini, Bharat B. AggarwalCurcumin, a component of the golden spice, is a highly pleiotropic molecule with anti-proliferative, anti-inflammatory, anti-oxidant, and anti-bacterial actions. How curcumin accomplish all these functions is the focus of this review. Curcumin's physical interaction with various signaling proteins is discussed.To cite this article before page numbers are assigned, use the DOI form of citation above.The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
            <author>RSC - Nat. Prod. Rep. latest articles</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5292336</comments>
            <pubDate>Fri, 07 Oct 2011 05:59:59 +0100</pubDate>
            <guid isPermaLink="false">5292336</guid>        </item>
        <item>
            <title>Combinatorial biosynthesis in plants: A (p)review on its potential and future exploitation</title>
            <link>http://www.medworm.com/index.php?rid=5268005&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2FGAKFLzEelL8%2FC1NP00049G</link>
            <description>Nat. Prod. Rep., 2011, Advance ArticleDOI: 10.1039/C1NP00049G, ReviewJacob Pollier, Tessa Moses, Alain GoossensThis review describes the state-of-the-art in combinatorial biochemistry methods that establish novel enzyme-substrate combinations in plants in vivo and lead to the biosynthesis of new, natural product-derived compounds that can be used in drug discovery programs.To cite this article before page numbers are assigned, use the DOI form of citation above.The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
            <author>RSC - Nat. Prod. Rep. latest articles</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5268005</comments>
            <pubDate>Fri, 30 Sep 2011 08:11:35 +0100</pubDate>
            <guid isPermaLink="false">5268005</guid>        </item>
        <item>
            <title>Pathways for degradation of lignin in bacteria and fungi</title>
            <link>http://www.medworm.com/index.php?rid=5232572&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2F2shkY9TG_iY%2FC1NP00042J</link>
            <description>This article describes recent progress in the understanding of the microbial breakdown of lignin, and catabolic pathways for the breakdown of lignin components.To cite this article before page numbers are assigned, use the DOI form of citation above.The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
            <author>RSC - Nat. Prod. Rep. latest articles</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5232572</comments>
            <pubDate>Mon, 19 Sep 2011 20:37:33 +0100</pubDate>
            <guid isPermaLink="false">5232572</guid>        </item>
        <item>
            <title>The sorbicillinoid family of natural products: Isolation, biosynthesis, and synthetic studies</title>
            <link>http://www.medworm.com/index.php?rid=5232571&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2Fl3pzlhz6sNY%2FC1NP00039J</link>
            <description>Nat. Prod. Rep., 2011, Advance ArticleDOI: 10.1039/C1NP00039J, ReviewAndrew M. Harned, Kelly A. VolpThe sorbicillinoids are a family of hexaketide fungal metabolites that have been isolated from both marine and terrestrial sources. The family (&amp;gt;50 members) is characterized by complex, highly oxygenated, bicyclic and tricyclic frameworks. We discuss the isolation, biological activity, biosynthesis, and chemical synthesis of the various family members.To cite this article before page numbers are assigned, use the DOI form of citation above.The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
            <author>RSC - Nat. Prod. Rep. latest articles</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5232571</comments>
            <pubDate>Mon, 19 Sep 2011 20:37:33 +0100</pubDate>
            <guid isPermaLink="false">5232571</guid>        </item>
        <item>
            <title>Natural products and Pharma 2011: Strategic changes spur new opportunities</title>
            <link>http://www.medworm.com/index.php?rid=5217295&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2FvusB95pr4JE%2FC1NP00033K</link>
            <description>Nat. Prod. Rep., 2011, Advance ArticleDOI: 10.1039/C1NP00033K, HighlightGuy T. CarterStrategic changes in the pharmaceutical industry once again favor drug discovery with natural products. Advances in genomics, chemistry and biotechnology combine to provide enhanced processes for the discovery and optimization of effective drugs derived from natural compounds.To cite this article before page numbers are assigned, use the DOI form of citation above.The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
            <author>RSC - Nat. Prod. Rep. latest articles</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5217295</comments>
            <pubDate>Wed, 14 Sep 2011 08:25:27 +0100</pubDate>
            <guid isPermaLink="false">5217295</guid>        </item>
        <item>
            <title>Hot off the Press</title>
            <link>http://www.medworm.com/index.php?rid=5203489&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2FSh60cC5vv2E%2FC1NP90035H</link>
            <description>Nat. Prod. Rep., 2011, Advance ArticleDOI: 10.1039/C1NP90035H, Hot off the Press ArticleRobert A. Hill, Andrew SutherlandA personal selection of 31 recent papers is presented covering various aspects of current developments in bioorganic chemistry and novel natural products such as artalbic acid from Artemisia alba.To cite this article before page numbers are assigned, use the DOI form of citation above.The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
            <author>RSC - Nat. Prod. Rep. latest articles</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5203489</comments>
            <pubDate>Sun, 11 Sep 2011 02:45:33 +0100</pubDate>
            <guid isPermaLink="false">5203489</guid>        </item>
        <item>
            <title>Enzymatic methods for glyco(diversification/randomization) of drugs and small molecules</title>
            <link>http://www.medworm.com/index.php?rid=5203488&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2FDgkjE_4KaWI%2FC1NP00045D</link>
            <description>Nat. Prod. Rep., 2011, Advance ArticleDOI: 10.1039/C1NP00045D, ReviewRichard W. Gantt, Pauline Peltier-Pain, Jon S. ThorsonGlyco(randomization/diversification) strategies enable the syntheses of differentially glycosylated drug libraries. This review covers the influence of glycosylation upon drug properties, the enzymes and substrates utilized in glyco(randomization/diversification) schemes and examples of glycorandomized libraries.To cite this article before page numbers are assigned, use the DOI form of citation above.The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
            <author>RSC - Nat. Prod. Rep. latest articles</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5203488</comments>
            <pubDate>Sun, 11 Sep 2011 02:45:33 +0100</pubDate>
            <guid isPermaLink="false">5203488</guid>        </item>
        <item>
            <title>The chemistry and biology of syringolins, glidobactins and cepafungins (syrbactins)</title>
            <link>http://www.medworm.com/index.php?rid=5203487&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2FJgxd_WvZWQU%2FC1NP00048A</link>
            <description>Nat. Prod. Rep., 2011, Advance ArticleDOI: 10.1039/C1NP00048A, ReviewDaniel Krahn, Christian Ottmann, Markus KaiserSyrbactin is a subordinate term for the syringolin, glidobactin and cepafungin natural product families. Their grouping is based on their related molecular frameworks, similar biosynthesis pathways and, most importantly, identical modes-of-action, being irreversible proteasome inhibition. With this report, we aim to review their chemical biology, describing their common, but also differential characteristics.To cite this article before page numbers are assigned, use the DOI form of citation above.The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
            <author>RSC - Nat. Prod. Rep. latest articles</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5203487</comments>
            <pubDate>Sun, 11 Sep 2011 02:45:33 +0100</pubDate>
            <guid isPermaLink="false">5203487</guid>        </item>
        <item>
            <title>Flavonoids and their glycosides, including anthocyanins</title>
            <link>http://www.medworm.com/index.php?rid=5137370&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2F0pe1VaWmo9E%2FC1NP00044F</link>
            <description>Nat. Prod. Rep., 2011, Advance ArticleDOI: 10.1039/C1NP00044F, ReviewNigel C. Veitch, Renee J. GrayerCovering research published on flavonoids between 2007 and 2009, more than 795 new aglycones and glycosides are described, comprising flavones, flavonols, chalcones, dihydrochalcones, aurones, flavanones, dihydroflavonols and anthocyanins.To cite this article before page numbers are assigned, use the DOI form of citation above.The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
            <author>RSC - Nat. Prod. Rep. latest articles</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5137370</comments>
            <pubDate>Wed, 17 Aug 2011 16:05:46 +0100</pubDate>
            <guid isPermaLink="false">5137370</guid>        </item>
        <item>
            <title>Hypervalent iodine reagents in the total synthesis of natural products</title>
            <link>http://www.medworm.com/index.php?rid=5116551&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2Fi2sZuiXKWSY%2FC1NP00028D</link>
            <description>This report describes the recent applications of hypervalent iodine reagents in the total synthesis of natural products. The large diversity of high-yielding and chemoselective reactions that can be achieved, even for highly functionalized molecules, is summarized, demonstrating that hypervalent iodine reagents have become an essential tool in synthetic organic chemistry.To cite this article before page numbers are assigned, use the DOI form of citation above.The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
            <author>RSC - Nat. Prod. Rep. latest articles</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5116551</comments>
            <pubDate>Thu, 11 Aug 2011 16:35:15 +0100</pubDate>
            <guid isPermaLink="false">5116551</guid>        </item>
        <item>
            <title>Natural sesquiterpenoids</title>
            <link>http://www.medworm.com/index.php?rid=5093754&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2FpwSmqAplVVU%2FC1NP00046B</link>
            <description>Nat. Prod. Rep., 2011, Advance ArticleDOI: 10.1039/C1NP00046B, ReviewBraulio M. FragaThis review covers the isolation, structural determination, synthesis and chemical and microbiological transformations of natural sesquiterpenoids reported in the literature of 2010.To cite this article before page numbers are assigned, use the DOI form of citation above.The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
            <author>RSC - Nat. Prod. Rep. latest articles</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5093754</comments>
            <pubDate>Thu, 04 Aug 2011 15:54:03 +0100</pubDate>
            <guid isPermaLink="false">5093754</guid>        </item>
        <item>
            <title>Platensimycin and its relatives: A recent story in the struggle to develop new naturally derived antibiotics</title>
            <link>http://www.medworm.com/index.php?rid=5093753&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2FZ7BjQe8oLgw%2FC1NP00010A</link>
            <description>Nat. Prod. Rep., 2011, Advance ArticleDOI: 10.1039/C1NP00010A, ReviewMuhammad Saleem, Hidayat Hussain, Ishtiaq Ahmed, Teunis van Ree, Karsten KrohnIn this review the isolation, occurrence, structure elucidation, chemical properties, biosynthesis and chemical synthesis of the naturally occurring cage-like antibiotics platensimycin, platencin, isoplatensimycin, platensimycin A1, and platensimycin B1-B3, as well as several synthetic analogues, are described. The literature up to 2010 is reviewed and 139 references are cited.To cite this article before page numbers are assigned, use the DOI form of citation above.The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
            <author>RSC - Nat. Prod. Rep. latest articles</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5093753</comments>
            <pubDate>Thu, 04 Aug 2011 15:54:03 +0100</pubDate>
            <guid isPermaLink="false">5093753</guid>        </item>
        <item>
            <title>Radical S-adenosylmethionine enzymes: Mechanism, control and function</title>
            <link>http://www.medworm.com/index.php?rid=5056994&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2FUyyuPZJ-528%2FC1NP00036E</link>
            <description>Nat. Prod. Rep., 2011, Advance ArticleDOI: 10.1039/C1NP00036E, ReviewMartin R. Challand, Rebecca C. Driesener, Peter L. RoachThis review describes progress in understanding the function of radical SAM enzymes, including the mechanism of radical formation and the wide range of subsequent biochemical steps.To cite this article before page numbers are assigned, use the DOI form of citation above.The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
            <author>RSC - Nat. Prod. Rep. latest articles</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5056994</comments>
            <pubDate>Sun, 24 Jul 2011 03:33:03 +0100</pubDate>
            <guid isPermaLink="false">5056994</guid>        </item>
        <item>
            <title>Similar interactions of natural products with biosynthetic enzymes and therapeutic targets could explain why nature produces such a large proportion of existing drugs</title>
            <link>http://www.medworm.com/index.php?rid=5056993&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2Fv6XlEKnVmgU%2FC1NP00026H</link>
            <description>Nat. Prod. Rep., 2011, Advance ArticleDOI: 10.1039/C1NP00026H, HighlightEsther Kellenberger, Andreas Hofmann, Ronald J. QuinnProtein Fold Topology (PFT) describes the imprint of biological interactions during biosynthesis. PFT correlations existing between biosynthetic enzymes and therapeutic targets could explain why so many natural products have become therapeutic agents. PFT represents a potential tool for drug design.To cite this article before page numbers are assigned, use the DOI form of citation above.The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
            <author>RSC - Nat. Prod. Rep. latest articles</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5056993</comments>
            <pubDate>Sun, 24 Jul 2011 03:33:03 +0100</pubDate>
            <guid isPermaLink="false">5056993</guid>        </item>
        <item>
            <title>Natural products containing a diazo group</title>
            <link>http://www.medworm.com/index.php?rid=5047693&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2F2DemBH1mTIo%2FC1NP00031D</link>
            <description>Nat. Prod. Rep., 2011, 28,1426-1444DOI: 10.1039/C1NP00031D, ReviewChristopher C. Nawrat, Christopher J. MoodyDiazo compounds, well known as intermediates in synthetic organic chemistry, also occur naturally. Some are simply modified [small alpha]-amino acids, whilst others are more complex, including diazonaphthoquinones, such as the SF2415 and A80915 antibiotics, and the diazofluorene-based kinamycins and lomaiviticins.The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
            <author>RSC - Nat. Prod. Rep. latest articles</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5047693</comments>
            <pubDate>Thu, 21 Jul 2011 23:00:08 +0100</pubDate>
            <guid isPermaLink="false">5047693</guid>        </item>
        <item>
            <title>Antibiotic activities of host defense peptides: more to it than lipid bilayer perturbation</title>
            <link>http://www.medworm.com/index.php?rid=5047692&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2F2I4u2G7nc2w%2FC1NP00022E</link>
            <description>Nat. Prod. Rep., 2011, 28,1350-1358DOI: 10.1039/C1NP00022E, HighlightMiriam Wilmes, Bruno P. A. Cammue, Hans-Georg Sahl, Karin ThevissenDefensins are generally presumed to unspecifically compromise lipid bilayers. This review summarizes recent reports on specific defensin targets, such as the bacterial cell wall precursor lipid II and fungal sphingolipids, which confer highly specific antibiotic activities to defensins.The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
            <author>RSC - Nat. Prod. Rep. latest articles</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5047692</comments>
            <pubDate>Thu, 21 Jul 2011 23:00:08 +0100</pubDate>
            <guid isPermaLink="false">5047692</guid>        </item>
        <item>
            <title>Natural products in anti-obesity therapy</title>
            <link>http://www.medworm.com/index.php?rid=5017243&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2F3LecFNKm7RE%2FC1NP00035G</link>
            <description>Nat. Prod. Rep., 2011, Advance ArticleDOI: 10.1039/C1NP00035G, ReviewIlze Vermaak, Alvaro M. Viljoen, Josias H. HammanObesity is a major health concern and should be considered a global epidemic. This review is an overview of scientific evidence collated for 50 commercially important plants that have been investigated for their anti-obesity effects.To cite this article before page numbers are assigned, use the DOI form of citation above.The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
            <author>RSC - Nat. Prod. Rep. latest articles</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5017243</comments>
            <pubDate>Tue, 12 Jul 2011 19:46:55 +0100</pubDate>
            <guid isPermaLink="false">5017243</guid>        </item>
        <item>
            <title>Piperazic acid-containing natural products: Isolation, biological relevance and total synthesis</title>
            <link>http://www.medworm.com/index.php?rid=5005728&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2FICRjfhLr_WQ%2FC1NP00041A</link>
            <description>Nat. Prod. Rep., 2011, Advance ArticleDOI: 10.1039/C1NP00041A, ReviewAlexander J. Oelke, David J. France, Tatjana Hofmann, Georg Wuitschik, Steven V. LeyNatural products containing the piperazic acid motif have been isolated from a variety of sources and exhibit diverse biological activity profiles. This review provides information about their isolation and biological activities, and presents an overview of recent total syntheses of these molecules.To cite this article before page numbers are assigned, use the DOI form of citation above.The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
            <author>RSC - Nat. Prod. Rep. latest articles</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5005728</comments>
            <pubDate>Thu, 07 Jul 2011 20:04:01 +0100</pubDate>
            <guid isPermaLink="false">5005728</guid>        </item>
        <item>
            <title>Metabolic engineering is key to a sustainable chemical industry</title>
            <link>http://www.medworm.com/index.php?rid=4982750&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2F9YINQAIBQxQ%2FC1NP00029B</link>
            <description>Nat. Prod. Rep., 2011, Advance ArticleDOI: 10.1039/C1NP00029B, ReviewAnnabel C. MurphyMetabolic engineering will be an increasingly valuable tool in reducing our reliance on non-renewable feedstocks for chemical production and improving the sustainability of the chemical industry.To cite this article before page numbers are assigned, use the DOI form of citation above.The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
            <author>RSC - Nat. Prod. Rep. latest articles</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4982750</comments>
            <pubDate>Thu, 30 Jun 2011 04:51:34 +0100</pubDate>
            <guid isPermaLink="false">4982750</guid>        </item>
        <item>
            <title>Plant volatiles: Production, function and pharmacology</title>
            <link>http://www.medworm.com/index.php?rid=4982749&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2Fud7CGRbvWUs%2FC1NP00021G</link>
            <description>Nat. Prod. Rep., 2011, Advance ArticleDOI: 10.1039/C1NP00021G, ReviewMassimo E. Maffei, Jurg Gertsch, Giovanni AppendinoThis review summarizes recent major developments in the study of biosynthesis, ecological functions and medicinal applications of plant volatile organic compounds (VOCs).To cite this article before page numbers are assigned, use the DOI form of citation above.The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
            <author>RSC - Nat. Prod. Rep. latest articles</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4982749</comments>
            <pubDate>Thu, 30 Jun 2011 04:51:34 +0100</pubDate>
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            <title>The phytoalexins from cultivated and wild crucifers: Chemistry and biology</title>
            <link>http://www.medworm.com/index.php?rid=4982748&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2FRUJna6XCbEM%2FC1NP00020A</link>
            <description>Nat. Prod. Rep., 2011, Advance ArticleDOI: 10.1039/C1NP00020A, ReviewM. Soledade C. Pedras, Estifanos E. Yaya, Erich GlawischnigThis review focuses on the phytoalexins produced by cruciferous plants, with particular emphasis on their synthesis, biosynthesis and metabolism by plant fungal pathogens and their biological activities.To cite this article before page numbers are assigned, use the DOI form of citation above.The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
            <author>RSC - Nat. Prod. Rep. latest articles</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4982748</comments>
            <pubDate>Thu, 30 Jun 2011 04:51:34 +0100</pubDate>
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        <item>
            <title>Anticancer compounds derived from fungal endophytes: their importance and future challenges</title>
            <link>http://www.medworm.com/index.php?rid=4982747&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2FAp-CkQB_VmE%2FC1NP00008J</link>
            <description>Nat. Prod. Rep., 2011, 28,1208-1228DOI: 10.1039/C1NP00008J, ReviewRavindra N. Kharwar, Ashish Mishra, Surendra K. Gond, Andrea Stierle, Donald StierleThis is a review of anticancer agents isolated from endophytic fungi from 1990-2010; some of the compounds have been previously isolated from higher plants. Endophytes are a dependable source of active metabolites, and can be manipulated to increase yields and to produce novel analogues of specific metabolites.The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
            <author>RSC - Nat. Prod. Rep. latest articles</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4982747</comments>
            <pubDate>Thu, 30 Jun 2011 04:51:34 +0100</pubDate>
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        <item>
            <title>Biosynthesis, asymmetric synthesis, and pharmacology, including cellular targets, of the pyrrole-2-aminoimidazole marine alkaloids</title>
            <link>http://www.medworm.com/index.php?rid=4982746&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2FlwiNn_mQdMM%2FC0NP00013B</link>
            <description>Nat. Prod. Rep., 2011, 28,1229-1260DOI: 10.1039/C0NP00013B, ReviewAli Al-Mourabit, Manuel A. Zancanella, Supriya Tilvi, Daniel RomoThe immense diversity of pyrrole-2-aminoimidazole alkaloids continues to 'spring forth' from various marine sponges (e.g. Stylissa caribica, orange). Biosynthetic speculations, enantioselective synthetic strategies, and biological studies of these unique alkaloids, including cellular receptor isolation, are reviewed.The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
            <author>RSC - Nat. Prod. Rep. latest articles</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4982746</comments>
            <pubDate>Thu, 30 Jun 2011 04:51:34 +0100</pubDate>
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        <item>
            <title>The saponins - polar isoprenoids with important and diverse biological activities</title>
            <link>http://www.medworm.com/index.php?rid=4982745&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2FnInlnZpPelI%2FC1NP00015B</link>
            <description>Nat. Prod. Rep., 2011, 28,1261-1268DOI: 10.1039/C1NP00015B, ReviewAnne Osbourn, Rebecca J. M. Goss, Robert A. FieldSaponins (glycosylated triterpenes and steroids) are 2,3-oxidosqualene-derived natural products with a wide range of applications in the food, cosmetics and pharmaceutical sectors. This review focuses on their biological activity, the relationship between structure and function, and on prospects for &quot;designer&quot; moleculesThe content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
            <author>RSC - Nat. Prod. Rep. latest articles</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4982745</comments>
            <pubDate>Thu, 30 Jun 2011 04:51:34 +0100</pubDate>
            <guid isPermaLink="false">4982745</guid>        </item>
        <item>
            <title>The regulation of the secondary metabolism of Streptomyces: new links and experimental advances</title>
            <link>http://www.medworm.com/index.php?rid=4982744&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2FwufhdCScMuQ%2FC1NP00003A</link>
            <description>Nat. Prod. Rep., 2011, 28,1311-1333DOI: 10.1039/C1NP00003A, ReviewGilles P. van Wezel, Kenneth J. McDowallWe review what is known about the control of secondary metabolite production in streptomycetes, with an emphasis on examples where details of the underlying regulatory mechanisms are known.The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
            <author>RSC - Nat. Prod. Rep. latest articles</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4982744</comments>
            <pubDate>Thu, 30 Jun 2011 04:51:34 +0100</pubDate>
            <guid isPermaLink="false">4982744</guid>        </item>
        <item>
            <title>Are we ready for industrial production of bioactive plant secondary metabolites utilizing endophytes?</title>
            <link>http://www.medworm.com/index.php?rid=4982743&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2F2DOazhqf4XQ%2FC1NP00030F</link>
            <description>Nat. Prod. Rep., 2011, 28,1203-1207DOI: 10.1039/C1NP00030F, ViewpointSouvik Kusari, Michael SpitellerIn this Viewpoint, the prospects and challenges of endophyte research is evaluated. Although endophytes are valuable alternate sources of associated plant compounds, further fundamental research is vital to address the trade-off between endophyte discovery and its sustainable commercial application, which holds the key in transforming endophytes into microbial manufacturers.The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
            <author>RSC - Nat. Prod. Rep. latest articles</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4982743</comments>
            <pubDate>Thu, 30 Jun 2011 04:51:34 +0100</pubDate>
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        <item>
            <title>Perspectives on the structural and biosynthetic interrelationships between oxygenated furanocembranoids and their polycyclic congeners found in corals</title>
            <link>http://www.medworm.com/index.php?rid=4982742&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2FY-7O2CF4RqY%2FC1NP00023C</link>
            <description>Nat. Prod. Rep., 2011, 28,1269-1310DOI: 10.1039/C1NP00023C, ReviewYi Li, Gerald PattendenA personal perspective on the structure relationships, and speculations on the likely biosynthetic interrelationships between macrocyclic furanocembranoids and their novel polycyclic, photochemical and oxidative rearranged congeners found in corals.The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
            <author>RSC - Nat. Prod. Rep. latest articles</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4982742</comments>
            <pubDate>Thu, 30 Jun 2011 04:51:34 +0100</pubDate>
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        <item>
            <title>Hot off the Press</title>
            <link>http://www.medworm.com/index.php?rid=4982741&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2Fq954_IsDQik%2FC1NP90027G</link>
            <description>Nat. Prod. Rep., 2011, Advance ArticleDOI: 10.1039/C1NP90027G, Hot off the Press ArticleRobert A. Hill, Andrew SutherlandA personal selection of 33 recent papers is presented covering various aspects of current developments in bioorganic chemistry and novel natural products, such as virgatolide A from Pestalotiopsis virgatula.To cite this article before page numbers are assigned, use the DOI form of citation above.The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
            <author>RSC - Nat. Prod. Rep. latest articles</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4982741</comments>
            <pubDate>Thu, 30 Jun 2011 04:51:34 +0100</pubDate>
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        <item>
            <title>Diterpenoids of terrestrial origin</title>
            <link>http://www.medworm.com/index.php?rid=4982740&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2FrFHUDEftT3o%2FC1NP90021H</link>
            <description>Nat. Prod. Rep., 2011, Advance ArticleDOI: 10.1039/C1NP90021H, ReviewJames R. HansonThis review covers the isolation and chemistry of diterpenoids from terrestrial as opposed to marine sources and includes labdanes, clerodanes, abietanes, pimaranes, kauranes, gibberellins, cembranes and their cyclization products and taxanes. The literature from January 2009 to December 2010 is reviewed.To cite this article before page numbers are assigned, use the DOI form of citation above.The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
            <author>RSC - Nat. Prod. Rep. latest articles</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4982740</comments>
            <pubDate>Thu, 30 Jun 2011 04:51:34 +0100</pubDate>
            <guid isPermaLink="false">4982740</guid>        </item>
        <item>
            <title>The phytoalexins from cultivated and wild crucifers: Chemistry and biology</title>
            <link>http://www.medworm.com/index.php?rid=4943983&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2F7WRmQppgatU%2F</link>
            <description>This review focuses on the phytoalexins produced by cruciferous plants, with particular emphasis on their synthesis, biosynthesis and metabolism by plant fungal pathogens and their biological activities.M. Soledade C. Pedras, Estifanos E. Yaya, Erich Glawischnig 
( from Nat. Prod. Rep.)
M. Soledade C. Pedras, Nat. Prod. Rep., 2011, DOI: 10.1039/C1NP00020A
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The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
            <author>RSC - Nat. Prod. Rep. latest articles</author>
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        <comments>http://www.medworm.com/rss/comments.php?id=4943983</comments>
            <pubDate>Thu, 16 Jun 2011 23:00:00 +0100</pubDate>
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        <item>
            <title>Metabolic engineering is key to a sustainable chemical industry</title>
            <link>http://www.medworm.com/index.php?rid=4931465&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2FYsB2dCRz6rk%2F</link>
            <description>Metabolic engineering will be an increasingly valuable tool in reducing our reliance on non-renewable feedstocks for chemical production and improving the sustainability of the chemical industry.Annabel C. Murphy 
( from Nat. Prod. Rep.)
Annabel C. Murphy, Nat. Prod. Rep., 2011, DOI: 10.1039/C1NP00029B
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The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
            <author>RSC - Nat. Prod. Rep. latest articles</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4931465</comments>
            <pubDate>Sun, 12 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4931465</guid>        </item>
        <item>
            <title>Plant volatiles: Production, function and pharmacology</title>
            <link>http://www.medworm.com/index.php?rid=4931464&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2FcIcVW5W0PVE%2F</link>
            <description>This review summarizes recent major developments in the study of biosynthesis, ecological functions and medicinal applications of plant volatile organic compounds (VOCs).Massimo E. Maffei, Jurg Gertsch, Giovanni Appendino 
( from Nat. Prod. Rep.)
Massimo E. Maffei, Nat. Prod. Rep., 2011, DOI: 10.1039/C1NP00021G
To cite this article before page numbers are assigned, use the DOI form of citation above.
The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
            <author>RSC - Nat. Prod. Rep. latest articles</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4931464</comments>
            <pubDate>Sun, 12 Jun 2011 23:00:00 +0100</pubDate>
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        <item>
            <title>Perspectives on the structural and biosynthetic interrelationships between oxygenated furanocembranoids and their polycyclic congeners found in corals</title>
            <link>http://www.medworm.com/index.php?rid=4900833&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2Fkszlj-Wjlmk%2F</link>
            <description>A personal perspective on the structure relationships, and speculations on the likely biosynthetic interrelationships between macrocyclic furanocembranoids and their novel polycyclic, photochemical and oxidative rearranged congeners found in corals.Yi Li, Gerald Pattenden 
( from Nat. Prod. Rep.)
Yi Li, Nat. Prod. Rep., 2011, DOI: 10.1039/C1NP00023C
To cite this article before page numbers are assigned, use the DOI form of citation above.
The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
            <author>RSC - Nat. Prod. Rep. latest articles</author>
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        <comments>http://www.medworm.com/rss/comments.php?id=4900833</comments>
            <pubDate>Thu, 02 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4900833</guid>        </item>
        <item>
            <title>Are we ready for industrial production of bioactive plant secondary metabolites utilizing endophytes?</title>
            <link>http://www.medworm.com/index.php?rid=4891155&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2Fv7FDPPb-fMw%2F</link>
            <description>In this Viewpoint, the prospects and challenges of endophyte research is evaluated. Although endophytes are valuable alternate sources of associated plant compounds, further fundamental research is vital to address the trade-off between endophyte discovery and its sustainable commercial application, which holds the key in transforming endophytes into microbial manufacturers.Souvik Kusari, Michael Spiteller 
( from Nat. Prod. Rep.)
Souvik Kusari, Nat. Prod. Rep., 2011, DOI: 10.1039/C1NP00030F
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The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
            <author>RSC - Nat. Prod. Rep. latest articles</author>
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        <comments>http://www.medworm.com/rss/comments.php?id=4891155</comments>
            <pubDate>Tue, 31 May 2011 23:00:00 +0100</pubDate>
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        <item>
            <title>Antibiotic activities of host defense peptides: more to it than lipid bilayer perturbation</title>
            <link>http://www.medworm.com/index.php?rid=4870313&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2FDg2ns6cBYdo%2F</link>
            <description>Defensins are generally presumed to unspecifically compromise lipid bilayers. This review summarizes recent reports on specific defensin targets, such as the bacterial cell wall precursor lipid II and fungal sphingolipids, which confer highly specific antibiotic activities to defensins.Miriam Wilmes, Bruno P. A. Cammue, Hans-Georg Sahl, Karin Thevissen 
( from Nat. Prod. Rep.)
Miriam Wilmes, Nat. Prod. Rep., 2011, DOI: 10.1039/C1NP00022E
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The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
            <author>RSC - Nat. Prod. Rep. latest articles</author>
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        <comments>http://www.medworm.com/rss/comments.php?id=4870313</comments>
            <pubDate>Thu, 26 May 2011 23:00:00 +0100</pubDate>
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        <item>
            <title>The regulation of the secondary metabolism of Streptomyces: new links and experimental advances</title>
            <link>http://www.medworm.com/index.php?rid=4860780&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2FHdkd4jPyd84%2F</link>
            <description>We review what is known about the control of secondary metabolite production in streptomycetes, with an emphasis on examples where details of the underlying regulatory mechanisms are known.Gilles P. van Wezel, Kenneth J. McDowall 
( from Nat. Prod. Rep.)
Gilles P. van Wezel, Nat. Prod. Rep., 2011, DOI: 10.1039/C1NP00003A
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The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
            <author>RSC - Nat. Prod. Rep. latest articles</author>
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        <comments>http://www.medworm.com/rss/comments.php?id=4860780</comments>
            <pubDate>Tue, 24 May 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4860780</guid>        </item>
        <item>
            <title>Natural products containing a diazo group</title>
            <link>http://www.medworm.com/index.php?rid=4839223&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2FmqG5yzIBLpQ%2F</link>
            <description>Diazo compounds, well known as intermediates in synthetic organic chemistry, also occur naturally. Some are simply modified [small alpha]-amino acids, whilst others are more complex, including diazonaphthoquinones, such as the SF2415 and A80915 antibiotics, and the diazofluorene-based kinamycins and lomaiviticins.Christopher C. Nawrat, Christopher J. Moody 
( from Nat. Prod. Rep.)
Christopher C. Nawrat, Nat. Prod. Rep., 2011, DOI: 10.1039/C1NP00031D
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        <comments>http://www.medworm.com/rss/comments.php?id=4839223</comments>
            <pubDate>Tue, 17 May 2011 23:00:00 +0100</pubDate>
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        <item>
            <title>The saponins - polar isoprenoids with important and diverse biological activities</title>
            <link>http://www.medworm.com/index.php?rid=4827323&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2FVv440eTKeOo%2F</link>
            <description>Saponins (glycosylated triterpenes and steroids) are 2,3-oxidosqualene-derived natural products with a wide range of applications in the food, cosmetics and pharmaceutical sectors. This review focuses on their biological activity, the relationship between structure and function, and on prospects for &quot;designer&quot; moleculesAnne Osbourn, Rebecca J. M. Goss, Robert A. Field 
( from Nat. Prod. Rep.)
Anne Osbourn, Nat. Prod. Rep., 2011, DOI: 10.1039/C1NP00015B
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The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
            <author>RSC - Nat. Prod. Rep. latest articles</author>
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        <comments>http://www.medworm.com/rss/comments.php?id=4827323</comments>
            <pubDate>Sun, 15 May 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4827323</guid>        </item>
        <item>
            <title>Biosynthesis, asymmetric synthesis, and pharmacology, including cellular targets, of the pyrrole-2-aminoimidazole marine alkaloids</title>
            <link>http://www.medworm.com/index.php?rid=4801446&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2Fu0FekuBv_Hw%2F</link>
            <description>The immense diversity of pyrrole-2-aminoimidazole alkaloids continues to 'spring forth' from various marine sponges (e.g. Stylissa caribica, orange). Biosynthetic speculations, enantioselective synthetic strategies, and biological studies of these unique alkaloids, including cellular receptor isolation, are reviewed.Ali Al-Mourabit, Manuel A. Zancanella, Supriya Tilvi, Daniel Romo 
( from Nat. Prod. Rep.)
Ali Al-Mourabit, Nat. Prod. Rep., 2011, DOI: 10.1039/C0NP00013B
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The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - Nat. Prod. Rep. latest articles)</description>
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        <comments>http://www.medworm.com/rss/comments.php?id=4801446</comments>
            <pubDate>Sun, 08 May 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4801446</guid>        </item>
        <item>
            <title>Convergent strategies in biosynthesis</title>
            <link>http://www.medworm.com/index.php?rid=4793879&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2FEdw64mtDGyQ%2F</link>
            <description>This review article focuses on how nature sometimes solves the same problem in the biosynthesis of small molecules but using very different approaches. Four examples, involving isopentenyldiphosphate, menaquinone, lysine, and aromatic polyketides, are highlightedTohru Dairi, Tomohisa Kuzuyama, Makoto Nishiyama, Isao Fujii 
( from Nat. Prod. Rep.)
Tohru Dairi, Nat. Prod. Rep., 2011, DOI: 10.1039/C0NP00047G
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        <comments>http://www.medworm.com/rss/comments.php?id=4793879</comments>
            <pubDate>Thu, 05 May 2011 23:00:00 +0100</pubDate>
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        <item>
            <title>Biosynthesis via carbocations: Theoretical studies on terpene formation</title>
            <link>http://www.medworm.com/index.php?rid=4787816&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2F0y0WPvGyf_8%2F</link>
            <description>Mechanistic studies making use of quantum chemical calculations to examine carbocation rearrangements proposed to occur during the biosynthesis of terpene natural products are reviewed.Dean J. Tantillo 
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Dean J. Tantillo, Nat. Prod. Rep., 2011, DOI: 10.1039/C1NP00006C
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            <pubDate>Tue, 03 May 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4787816</guid>        </item>
        <item>
            <title>Hot off the press</title>
            <link>http://www.medworm.com/index.php?rid=4779501&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2FyWa5KhpsHy8%2F</link>
            <description>A personal selection of 30 recent papers is presented covering various aspects of current developments in bioorganic chemistry and novel natural products, such as salvileucalin C from Salvia leucantha.Robert A. Hill, Andrew Sutherland 
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Robert A. Hill, Nat. Prod. Rep., 2011, DOI: 10.1039/C1NP90013G
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            <pubDate>Mon, 02 May 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4779501</guid>        </item>
        <item>
            <title>Triterpenoids</title>
            <link>http://www.medworm.com/index.php?rid=4762097&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2FNe9A4-2Ihx0%2F</link>
            <description>This review covers the isolation and structure determination of triterpenoids, including squalene derivatives, protostanes, lanostanes, holostanes, cycloartanes, dammaranes, euphanes, tirucallanes, tetranortriterpenoids, quassinoids, lupanes, oleananes, friedelanes, ursanes, hopanes, serratanes and saponins. The literature from January 2009 to December 2009 is reviewed and 278 references are cited.Robert A. Hill, Joseph D. Connolly 
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Robert A. Hill, Nat. Prod. Rep., 2011, DOI: 10.1039/C1NP00012H
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            <pubDate>Wed, 27 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4762097</guid>        </item>
        <item>
            <title>Application of NMR methods to the study of the interaction of natural products with biomolecular receptors</title>
            <link>http://www.medworm.com/index.php?rid=4703124&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2FFRHgPO0UR5U%2F</link>
            <description>Nuclear magnetic resonance is a powerful tool that permits access to detailed knowledge of the interactions between natural products and their receptors, with atomic and molecular resolution. In this review, selected examples of the application of various NMR-based techniques are described.Luis P. Calle, F. Javier Canada, Jesus Jimenez-Barbero 
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Luis P. Calle, Nat. Prod. Rep., 2011, DOI: 10.1039/C0NP00071J
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            <pubDate>Mon, 11 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4703124</guid>        </item>
        <item>
            <title>Amaryllidaceae and Sceletium alkaloids</title>
            <link>http://www.medworm.com/index.php?rid=4682393&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2Fb0W3yfbQ0S4%2F</link>
            <description>Recent progress on the isolation, identification, biological activity, and chemical synthesis of Amaryllidaceae alkaloids and the structurally close Sceletium alkaloids is reviewed, and the literature covered from July 2008 to June 2010.Zhong Jin 
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Zhong Jin, Nat. Prod. Rep., 2011, DOI: 10.1039/C0NP00073F
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            <pubDate>Wed, 06 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4682393</guid>        </item>
        <item>
            <title>Muscarine, imidazole, oxazole, and thiazole alkaloids</title>
            <link>http://www.medworm.com/index.php?rid=4682392&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2F7AGm8eqfyDQ%2F</link>
            <description>Recent progress on the isolation, identification, biological activities, and chemical synthesis of imidazole-, oxazole- and thiazole-containing natural products is summarized in this review and the literature covered from July 2007 to June 2010.Zhong Jin 
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Zhong Jin, Nat. Prod. Rep., 2011, DOI: 10.1039/C0NP00074D
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            <pubDate>Wed, 06 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4682392</guid>        </item>
        <item>
            <title>Anticancer compounds derived from fungal endophytes: their importance and future challenges</title>
            <link>http://www.medworm.com/index.php?rid=4669073&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2FT1yUM9Y5kgg%2F</link>
            <description>This is a review of anticancer agents isolated from endophytic fungi from 1990-2010; some of the compounds have been previously isolated from higher plants. Endophytes are a dependable source of active metabolites, and can be manipulated to increase yields and to produce novel analogues of specific metabolites.Ravindra N. Kharwar, Ashish Mishra, Surendra K. Gond, Andrea Stierle, Donald Stierle 
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Ravindra N. Kharwar, Nat. Prod. Rep., 2011, DOI: 10.1039/C1NP00008J
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            <pubDate>Thu, 31 Mar 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4669073</guid>        </item>
        <item>
            <title>Synthetic glycosylphosphatidylinositol (GPI) anchors: how these complex molecules have been made</title>
            <link>http://www.medworm.com/index.php?rid=4657659&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2FEbrWTqyEImI%2F</link>
            <description>Glycosylphosphatidylinositols are a class of natural glycosylphospholipids that anchor proteins, glycoproteins and lipophosphoglycans to the membrane of eukaryotic cells. This comprehensive review highlights the progress in the chemical synthesis of GPI anchors from protozoan parasites, yeast and mammals in the last two decades.Andrei V. Nikolaev, Nawaf Al-Maharik 
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Andrei V. Nikolaev, Nat. Prod. Rep., 2011, DOI: 10.1039/C0NP00064G
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            <pubDate>Tue, 29 Mar 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4657659</guid>        </item>
        <item>
            <title>Synthetic approaches to oligomeric natural products</title>
            <link>http://www.medworm.com/index.php?rid=4641177&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2FQXFJ6rG8BKs%2F</link>
            <description>This review aims to provide a comprehensive summary of known oligomeric natural product families whose structures are classified as either serial or non-serial based on their mode of construction. Synthetic approaches toward the general synthesis of families of oligomeric natural products are also discussed through seven case studies.Scott A. Snyder, Adel M. ElSohly, Ferenc Kontes 
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Scott A. Snyder, Nat. Prod. Rep., 2011, DOI: 10.1039/C1NP00001B
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            <pubDate>Thu, 17 Mar 2011 00:00:00 +0100</pubDate>
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        <item>
            <title>Bufadienolides and their antitumor activity</title>
            <link>http://www.medworm.com/index.php?rid=4641176&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2F28lWTR-PHdM%2F</link>
            <description>This review summarizes both new bufadienolides and those obtained from new sources, together with data regarding the antitumor activity of bufadienolide derivatives.Huimin Gao, Ruxandra Popescu, Brigitte Kopp, Zhimin Wang 
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Huimin Gao, Nat. Prod. Rep., 2011, DOI: 10.1039/C0NP00032A
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            <pubDate>Thu, 17 Mar 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4641176</guid>        </item>
        <item>
            <title>Synthetic approaches to oligomeric natural products</title>
            <link>http://www.medworm.com/index.php?rid=4604983&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Fxlink.rsc.org%2F%3FDOI%3Dc1np00001b%26RSS%3D1</link>
            <description>Scott A. Snyder, Adel M. ElSohly, Ferenc Kontes 
(Review from Nat. Prod. Rep.)
Scott A. Snyder, Nat. Prod. Rep., 2011, DOI: 10.1039/c1np00001b
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            <pubDate>Thu, 17 Mar 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4604983</guid>        </item>
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            <title>Propolis research and the chemistry of plant products</title>
            <link>http://www.medworm.com/index.php?rid=4641178&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2FR3OiPV7pQcM%2F</link>
            <description>This review describes the plant origin, geographic distribution and chemical composition of propolis, a honeybee product composed mainly of wax and plant-derived resins.Antonio Salatino, Caroline C. Fernandes-Silva, Adne Abbud Righi, Maria Luiza F. Salatino 
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Antonio Salatino, Nat. Prod. Rep., 2011, DOI: 10.1039/C0NP00072H
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            <pubDate>Wed, 16 Mar 2011 00:00:00 +0100</pubDate>
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        <item>
            <title>Glycosides as compatible solutes: biosynthesis and applications</title>
            <link>http://www.medworm.com/index.php?rid=4641179&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2FAvp56eP5pUo%2F</link>
            <description>Glycosides constitute an important class of natural solutes that protect cells against hyperosmolality of the extracellular environment. In this review, we cover their structural diversity and the enzymology of their biosynthesis, as well as presenting their potential uses in health-care, cosmetic and food applications.Christiane Luley-Goedl, Bernd Nidetzky 
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Christiane Luley-Goedl, Nat. Prod. Rep., 2011, DOI: 10.1039/C0NP00067A
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            <pubDate>Thu, 10 Mar 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4641179</guid>        </item>
        <item>
            <title>Hot off the press</title>
            <link>http://www.medworm.com/index.php?rid=4641180&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2FVhTxmHqfJSA%2F</link>
            <description>A personal selection of 27 recent papers is presented covering various aspects of current developments in bioorganic chemistry and novel natural products such as dibelamcandal A from Belamcanda chinensis.Robert A. Hill, Andrew Sutherland 
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Robert A. Hill, Nat. Prod. Rep., 2011, DOI: 10.1039/C1NP90009A
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            <pubDate>Wed, 09 Mar 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4641180</guid>        </item>
        <item>
            <title>Natural glycans and glycoconjugates as immunomodulating agents</title>
            <link>http://www.medworm.com/index.php?rid=4641181&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2FOP-bUaDpnIk%2F</link>
            <description>An overview of natural oligo- and polysaccharides that trigger immune responses is provided. This review will discuss their biological effects on immunocompetent cells, and how they are dependent on both the structures of the molecular targets and their receptors. Some applications will be also emphasized.Ilona Chlubnova, Balla Sylla, Caroline Nugier-Chauvin, Richard Daniellou, Laurent Legentil, Blanka Kralova, Vincent Ferrieres 
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Ilona Chlubnova, Nat. Prod. Rep., 2011, DOI: 10.1039/C1NP00005E
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            <pubDate>Fri, 04 Mar 2011 00:00:00 +0100</pubDate>
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        <item>
            <title>Natural withanolides: an overview</title>
            <link>http://www.medworm.com/index.php?rid=4641182&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2FCZ8C3eH0P-Y%2F</link>
            <description>This review provides a comprehensive summary of the structural classification and distribution of new withanolide steroids reported between August 1996 to March 2010, in addition to discussing their diverse biological and pharmacological activities.Li-Xia Chen, Hao He, Feng Qiu 
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Li-Xia Chen, Nat. Prod. Rep., 2011, DOI: 10.1039/C0NP00045K
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            <pubDate>Wed, 23 Feb 2011 00:00:00 +0100</pubDate>
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        <item>
            <title>Anticonvulsant neuropeptides as drug leads for neurological diseases</title>
            <link>http://www.medworm.com/index.php?rid=4641183&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Ffeeds.rsc.org%2F%7Er%2Frss%2FNP%2F%7E3%2FmFA9jKht01A%2F</link>
            <description>This review provides an overview of structural and pharmacological properties for selected anticonvulsant neuropeptides and their analogs, aiming to encourage broader efforts to convert these endogenous natural products into drug leads for pain, epilepsy and other neurological diseases.Charles R. Robertson, Sean P. Flynn, H. Steve White, Grzegorz Bulaj 
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Charles R. Robertson, Nat. Prod. Rep., 2011, DOI: 10.1039/C0NP00048E
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            <pubDate>Mon, 21 Feb 2011 00:00:00 +0100</pubDate>
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        <item>
            <title>Mode of action and biosynthesis of the azabicycle-containing natural products azinomycin and ficellomycin</title>
            <link>http://www.medworm.com/index.php?rid=4481730&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Fxlink.rsc.org%2F%3FDOI%3Dc0np00049c%26RSS%3D1</link>
            <description>Jennifer Foulke-Abel, Hillary Agbo, Huitu Zhang, Shogo Mori, Coran M. H. Watanabe 
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Jennifer Foulke-Abel, Nat. Prod. Rep., 2011, DOI: 10.1039/c0np00049c
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            <pubDate>Tue, 15 Feb 2011 00:00:00 +0100</pubDate>
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        <item>
            <title>Carotenoids and their cleavage products: Biosynthesis and functions</title>
            <link>http://www.medworm.com/index.php?rid=4476733&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Fxlink.rsc.org%2F%3FDOI%3Dc0np00036a%26RSS%3D1</link>
            <description>Michael H. Walter, Dieter Strack 
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Michael H. Walter, Nat. Prod. Rep., 2011, DOI: 10.1039/c0np00036a
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            <pubDate>Mon, 14 Feb 2011 00:00:00 +0100</pubDate>
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            <title>Synthesis of ellagitannin natural products</title>
            <link>http://www.medworm.com/index.php?rid=4476732&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Fxlink.rsc.org%2F%3FDOI%3Dc0np00058b%26RSS%3D1</link>
            <description>Laurent Pouysegu, Denis Deffieux, Gaelle Malik, Anna Natangelo, Stephane Quideau 
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Laurent Pouysegu, Nat. Prod. Rep., 2011, DOI: 10.1039/c0np00058b
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            <pubDate>Mon, 14 Feb 2011 00:00:00 +0100</pubDate>
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            <title>Xanthane sesquiterpenoids: structure, synthesis and biological activity</title>
            <link>http://www.medworm.com/index.php?rid=4476731&amp;cid=s_33810_59_f&amp;fid=33810&amp;url=http%3A%2F%2Fxlink.rsc.org%2F%3FDOI%3Dc0np00011f%26RSS%3D1</link>
            <description>Andrea Vasas, Judit Hohmann 
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Andrea Vasas, Nat. Prod. Rep., 2011, DOI: 10.1039/c0np00011f
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