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		<title>Molecules: Natural Products: Acetogenins: Extraction, Synthesis and Biological Properties</title>
		<link>http://www.mdpi.com/journal/molecules/special_issues/acetogenins/</link>
		<description>Submission 
All papers should be submitted to molecules@mdpi.com with copy to the guest editor. To be published continuously until the deadline and papers will be listed together at the special websites.
Submitted papers should not have been previously published nor be currently under consideration for publication elsewhere. All papers are refereed through a peer review process. A guide for authors, sample copies and other relevant information for submitting papers are available on the Instructions for Authors page. Molecules is an international peer-reviewed monthly journal published by MDPI.
Please visit the Instructions for Authors page before submitting a paper. Open Access publication fees are 800 CHF per paper. English correction fees (250 CHF) will be added in certain cases (1050 CHF per paper for those papers that require extensive additional formatting and/or English corrections).</description>
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	<title>Molecules, Vol. 15, Pages 460-501: Total Synthesis of Annonaceous Acetogenins Belonging to the Non-Adjacent Bis-THF and Non-Adjacent THF-THP Sub-Classes</title>
	<link>http://www.mdpi.com/1420-3049/15/1/460/</link>
	<description>The synthesis of the subgroups of acetogenins containing non-adjacent bis-THF and non-adjacent THF-THP core units is reviewed. Specifically, total syntheses of gigantecin, 4-deoxygigantecin, cis-sylvaticin, squamostatin-C, squamostatin-D, sylvaticin and mucocin are discussed.</description>
	
	<guid>http://www.mdpi.com/1420-3049/15/1/460/</guid>
	<pubDate>Thu, 21 Jan 2010 00:00:00 CET</pubDate>
	
	<prism:publicationName>Molecules</prism:publicationName>
	<prism:publicationDate>2010-01-21</prism:publicationDate>
	<prism:volume>15</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Review</prism:section>
	<prism:startingPage>460</prism:startingPage>
		<prism:endingPage>501</prism:endingPage>
		<prism:issn>1420-3049</prism:issn>
	
	<dc:title>Total Synthesis of Annonaceous Acetogenins Belonging to the Non-Adjacent Bis-THF and Non-Adjacent THF-THP Sub-Classes</dc:title>
	<dc:date>2010-01-21</dc:date>
	<dc:identifier>doi: 10.3390/molecules15010460</dc:identifier>
		<dc:creator>Ian  B. Spurr</dc:creator>
		<dc:creator>Richard C. D. Brown</dc:creator>
	
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	<item rdf:about="http://www.mdpi.com/1420-3049/14/12/5235/">
	<title>Molecules, Vol. 14, Pages 5235-5246: MALDI-TOF MS Profiling of Annonaceous Acetogenins in Annona muricata Products for Human Consumption</title>
	<link>http://www.mdpi.com/1420-3049/14/12/5235/</link>
	<description>Annonaceous acetogenins are proposed as environmental neurotoxicants consumed through medicinal and alimentary habits and responsible for atypical parkinsonian syndromes observed in tropical areas. Potential sources of exposure still have to be determined, as, to date, only a few batches of products for human consumption were searched for these compounds. To assess the presence of acetogenins, we propose a fast, sensitive and accurate method of screening, using MALDI-TOF MS, with minimal sample preparation. Development of the technique is discussed. Its application to leaves of herbal tea, pulp and bottled nectar of Annona muricata is presented.</description>
	
	<guid>http://www.mdpi.com/1420-3049/14/12/5235/</guid>
	<pubDate>Tue, 15 Dec 2009 00:00:00 CET</pubDate>
	
	<prism:publicationName>Molecules</prism:publicationName>
	<prism:publicationDate>2009-12-15</prism:publicationDate>
	<prism:volume>14</prism:volume>
	<prism:number>12</prism:number>
	<prism:section>Communication</prism:section>
	<prism:startingPage>5235</prism:startingPage>
		<prism:endingPage>5246</prism:endingPage>
		<prism:issn>1420-3049</prism:issn>
	
	<dc:title>MALDI-TOF MS Profiling of Annonaceous Acetogenins in Annona muricata Products for Human Consumption</dc:title>
	<dc:date>2009-12-15</dc:date>
	<dc:identifier>doi: 10.3390/molecules14125235</dc:identifier>
		<dc:creator>Pierre Champy</dc:creator>
		<dc:creator>Vincent Guérineau</dc:creator>
		<dc:creator>Olivier Laprévote</dc:creator>
	
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	<item rdf:about="http://www.mdpi.com/1420-3049/14/11/4387/">
	<title>Molecules, Vol. 14, Pages 4387-4395: Apolar Annonaceous Acetogenins from the Fruit Pulp of Annona muricata</title>
	<link>http://www.mdpi.com/1420-3049/14/11/4387/</link>
	<description>A methylene chloride extract of the pulp of Annona muricata L. was fractionated in search for scarcely functionalized Annonaceous acetogenins (type E). Previously known C-35 and C-37 mono-epoxy unsaturated compounds, epomuricenins-A and -B (1+2) and epomusenins-A and -B (3+4), were obtained. Two new mono-epoxy saturated C-35 representatives, epomurinins-A and -B (5+6) were also isolated.</description>
	
	<guid>http://www.mdpi.com/1420-3049/14/11/4387/</guid>
	<pubDate>Mon, 02 Nov 2009 00:00:00 CET</pubDate>
	
	<prism:publicationName>Molecules</prism:publicationName>
	<prism:publicationDate>2009-11-02</prism:publicationDate>
	<prism:volume>14</prism:volume>
	<prism:number>11</prism:number>
	<prism:section>Communication</prism:section>
	<prism:startingPage>4387</prism:startingPage>
		<prism:endingPage>4395</prism:endingPage>
		<prism:issn>1420-3049</prism:issn>
	
	<dc:title>Apolar Annonaceous Acetogenins from the Fruit Pulp of Annona muricata</dc:title>
	<dc:date>2009-11-02</dc:date>
	<dc:identifier>doi: 10.3390/molecules14114387</dc:identifier>
		<dc:creator>Alice Melot</dc:creator>
		<dc:creator>Djibril Fall</dc:creator>
		<dc:creator>Christophe Gleye</dc:creator>
		<dc:creator>Pierre Champy</dc:creator>
	
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	<item rdf:about="http://www.mdpi.com/1420-3049/14/9/3621/">
	<title>Molecules, Vol. 14, Pages 3621-3661: Medicinal Chemistry of Annonaceous Acetogenins: Design, Synthesis, and Biological Evaluation of Novel Analogues</title>
	<link>http://www.mdpi.com/1420-3049/14/9/3621/</link>
	<description>Most Annonaceous acetogenins are characterized by between one and three THF ring(s) with one or two flanking hydroxyl group(s) in the center of a C32/34 fatty acid, and the terminal carboxylic acid is combined with a 2-propanol unit to form an α,β-unsaturated γ-lactone. While many studies have addressed the properties and synthesis of natural acetogenins due to their attractive biological activities and unique structural features, a number of analogues have also been described. This review covers the design, synthesis, and biological evaluation of acetogenin analogues.</description>
	
	<guid>http://www.mdpi.com/1420-3049/14/9/3621/</guid>
	<pubDate>Thu, 17 Sep 2009 00:00:00 CEST</pubDate>
	
	<prism:publicationName>Molecules</prism:publicationName>
	<prism:publicationDate>2009-09-17</prism:publicationDate>
	<prism:volume>14</prism:volume>
	<prism:number>9</prism:number>
	<prism:section>Review</prism:section>
	<prism:startingPage>3621</prism:startingPage>
		<prism:endingPage>3661</prism:endingPage>
		<prism:issn>1420-3049</prism:issn>
	
	<dc:title>Medicinal Chemistry of Annonaceous Acetogenins: Design, Synthesis, and Biological Evaluation of Novel Analogues</dc:title>
	<dc:date>2009-09-17</dc:date>
	<dc:identifier>doi: 10.3390/molecules14093621</dc:identifier>
		<dc:creator>Naoto Kojima</dc:creator>
		<dc:creator>Tetsuaki Tanaka</dc:creator>
	
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