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image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Vector-Borne and Zoo...arrow_drop_down
image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao
Vector-Borne and Zoonotic Diseases
Article . 2006 . Peer-reviewed
License: Mary Ann Liebert TDM
Data sources: Crossref
Vector-Borne and Zoonotic Diseases
Article . 2006
Data sources: Europe PubMed Central
https://dx.doi.org/10.1089/vbz...
Article
Data sources: Microsoft Academic Graph
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Larvicidal Diterpenes from Pterodon polygalaeflorus

descriptionPublicationkeyboard_double_arrow_right Article 01 Jun 2006 English Publisher:SAGE PublicationsJournal:Vector-Borne and Zoonotic Diseases, volume 6, pages 216-222 (issn: 1530-3667, eissn: 1557-7759, Copyright policy )
Authors: M C, De Omena; E S, Bento; J E, De Paula; A E G, Sant'Ana;

doi: 10.1089/vbz.2006.6.216

pmid: 16796519

Larvicidal Diterpenes from Pterodon polygalaeflorus

Abstract

Ethanolic extract from seeds of Pterodon polygalaeflorus (Benth) has been shown to possess significant larvicidal activity against the mosquito Aedes aegypti. Bioassay-guided fractionation of the extract led to the isolation and characterization of the know diterpenoid furans 6alpha-hydroxyvouacapan-7beta,17beta-lactone (1), 6alpha,7beta-dihydroxyvouacapan- 17beta-oic acid (2) and methyl 6alpha,7beta-dihydroxyvouacapan-17beta-oate (3). The structures were established from infrared (IR), ultraviolet (UV), 1H-nuclear magnetic resonance (NMR), 13C-NMR, and mass spectral data: full NMR assignments are presented for compounds 1-3 and the diacetyl derivative of 3. Compounds 1-3 exhibited LC50 values of 50.08, 14.69, and 21.76 microg/mL against fourth-instar Aedes aegypti larvae.

Related Organizations
Keywords

Insecticides, Magnetic Resonance Spectroscopy, Plant Extracts, Fabaceae, Aedes, Larva, Seeds, Animals, Biological Assay, Diterpenes, Pest Control, Biological

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    popularity
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    		 Top 10%
    influence
    This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
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    impulse
    This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
34
Top 10%
Top 10%
Top 10%
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