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<!DOCTYPE ArticleSet PUBLIC "-//NLM//DTD PubMed 2.7//EN" "https://dtd.nlm.nih.gov/ncbi/pubmed/in/PubMed.dtd">
<ArticleSet>
<Article>
<Journal>
<PublisherName>OICC Press</PublisherName>
<JournalTitle>Trends in Phytochemical Research</JournalTitle>
<Issn>2588-3631</Issn>
<Volume>3</Volume>
<Issue>4</Issue>
<PubDate PubStatus="epublish">
<Year>2019</Year>
<Month>12</Month>
<Day>01</Day>
</PubDate>
</Journal>
<ArticleTitle>Flavonol glycosides with insecticidal activity from methanol extract of Annona mucosa leave</ArticleTitle>
<VernacularTitle></VernacularTitle>
<FirstPage>287</FirstPage>
<LastPage>296</LastPage>
<ELocationID EIdType="doi"></ELocationID>
<Language>EN</Language>
<AuthorList>
<Author>
<FirstName>Albert Mulianga</FirstName>
<LastName>Makenzi</LastName>
<Affiliation>Chemistry Department, Maseno University, P. O. Box 333-40105 Maseno, Kenya</Affiliation>
<Identifier Source="ORCID"></Identifier>
</Author>
<Author>
<FirstName>Lawrence Onyango Arot</FirstName>
<LastName>Manguro</LastName>
<Affiliation>Chemistry Department, Maseno University, P. O. Box 333-40105 Maseno, Kenya</Affiliation>
<Identifier Source="ORCID"></Identifier>
</Author>
<Author>
<FirstName>Philip Okinda</FirstName>
<LastName>Owuor</LastName>
<Affiliation>Chemistry Department, Maseno University, P. O. Box 333-40105 Maseno, Kenya</Affiliation>
<Identifier Source="ORCID"></Identifier>
</Author>
<Author>
<FirstName>Sylvia Awino</FirstName>
<LastName>Opiyo</LastName>
<Affiliation>Chemistry Department, Murang&amp;rsquo;a University, P.O. Box 75-10200, Muranga, Kenya</Affiliation>
<Identifier Source="ORCID"></Identifier>
</Author>
</AuthorList>
<PublicationType>Journal Article</PublicationType>
<History>
<PubDate PubStatus="received">
<Year>2019</Year>
<Month>12</Month>
<Day>01</Day>
</PubDate>
</History>
<Abstract>Three flavonoids, quercetin 3-O-&amp;beta;-D-glucoside (1), quercetin 3-O-&amp;alpha;-D-arabinoside (2) and kaempferol 3-O-&amp;beta;-D-galactoside (3) were isolated from the methanol leaf extract of Annona mucosa. Their structures were determined using physical and spectroscopic methods. compound 1 showed the highest activity against both S. zeamais and P. truncatus with LC50 values of 20.891 &amp;mu;g/ml and 22.241&amp;mu;g/ml, respectively though lower than the activity of deltamethrine a commercial insecticide used as a positive control. Compounds 2 and 3 gave moderate toxicities with LC50 values of 21.745 &amp;mu;g/ml and 24.926 &amp;mu;g/ml for compound 2 and 29.260&amp;mu;g/ml and 24.241&amp;mu;g/ml for compound 3 when tested against S. zeamais and P. truncates, respectively. compounds 1, 2 and 3 were also tested for anti-feedant activities against S. zeamais and P. truncatus and they exhibited interesting results. The activities were concentration dependent, increasing with increase in concentration. Quercetin 3-O-&amp;beta;-D-glucoside (1) showed the highest activities with AFI50 values 14.856 &amp;micro;g/ml and 16.79 &amp;micro;g/ml against S. zeamais and P. truncatus respectively (Figure 3). This actvity was close to but lower than the activity of azadirachtin a commercial antifeedant that had an activity of AFI50 of 12.146 &amp;micro;g/ml and 12.432 &amp;micro;g/ml against S. zeamais and P. truncates, respectively. Compounds 2 and 3 also exhibited relatively high antifeedant activities with values of AFI50 values 17.257&amp;micro;g/ml and AFI50 19.965&amp;micro;g/ml for compound 2 while values of AFI50 21.599 &amp;micro;g/ml and 20.149 &amp;micro;g/ml were obtained for compound 3 respectively, when tested against S. zeamais and P. truncatus respectively.</Abstract>
<ObjectList>
<Object Type="keyword">
<Param Name="value">&lt;i&gt;Annona mucosa&lt;/i&gt;</Param>
</Object>
<Object Type="keyword">
<Param Name="value">&lt;i&gt;Sitophilus zeamais&lt;/i&gt;</Param>
</Object>
<Object Type="keyword">
<Param Name="value">flavonol gycosides</Param>
</Object>
<Object Type="keyword">
<Param Name="value">insecticidal activities</Param>
</Object>
<Object Type="keyword">
<Param Name="value">&lt;i&gt;Prostephanus truncatus&lt;/i&gt;</Param>
</Object>
</ObjectList>
</Article>
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