Literature DB >> 16608209

Insecticidal activity of Paraherquamides, including paraherquamide H and paraherquamide I, two new alkaloids isolated from Penicillium cluniae.

M Pilar López-Gresa1, M Carmen González, Letizia Ciavatta, Ildefonso Ayala, Pilar Moya, Jaime Primo.   

Abstract

Paraherquamide H (1) and paraherquamide I (2), two new compounds of the paraherquamide (PHQ) family, together with the already known paraherquamide A (3), paraherquamide B (4), paraherquamide E (5), VM55596 (N-oxide paraherquamide) (6), paraherquamide VM55597 (7), and five known diketopiperazines (8-12) have been isolated from the culture broth of Penicillium cluniae Quintanilla. The structure of 1 and 2, on the basis of NMR and MS analysis, was established. It is worth noticing that, in both cases, an unusual oxidative substitution in C-16 was found, which had only previously been detected in PHQ 7. Isolated compounds were tested for insecticidal activity against the hemipteran Oncopeltus fasciatus Dallas. Mortality data have allowed preliminary structure activity relationships to be proposed. The most potent product was 5 with a LD(50) of 0.089 microg/nymph.

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Year:  2006        PMID: 16608209     DOI: 10.1021/jf0530998

Source DB:  PubMed          Journal:  J Agric Food Chem        ISSN: 0021-8561            Impact factor:   5.279


  10 in total

1.  Studies Towards Paraherquamides E & F and Related C-labeled Putative Biosynthetic Intermediates: Stereocontrolled Synthesis of the α-Alkyl-β-Methylproline Ring System.

Authors:  Konrad Sommer; Robert M Williams
Journal:  Tetrahedron       Date:  2008-07-21       Impact factor: 2.457

Review 2.  Fungal origins of the bicyclo[2.2.2]diazaoctane ring system of prenylated indole alkaloids.

Authors:  Jennifer M Finefield; Jens C Frisvad; David H Sherman; Robert M Williams
Journal:  J Nat Prod       Date:  2012-04-15       Impact factor: 4.050

3.  Classification of Aspergillus, Penicillium, Talaromyces and related genera (Eurotiales): An overview of families, genera, subgenera, sections, series and species.

Authors:  J Houbraken; S Kocsubé; C M Visagie; N Yilmaz; X-C Wang; M Meijer; B Kraak; V Hubka; K Bensch; R A Samson; J C Frisvad
Journal:  Stud Mycol       Date:  2020-06-27       Impact factor: 16.097

4.  Synthesis of functionalized indolizidines through Pauson-Khand cycloaddition of 2-allylpyrrolidines.

Authors:  Michael P McCormack; Stephen P Waters
Journal:  J Org Chem       Date:  2013-01-23       Impact factor: 4.354

Review 5.  Enzyme evolution in fungal indole alkaloid biosynthesis.

Authors:  Amy E Fraley; David H Sherman
Journal:  FEBS J       Date:  2020-04       Impact factor: 5.542

6.  Rapid access to spirocyclic oxindole alkaloids: application of the asymmetric palladium-catalyzed [3 + 2] trimethylenemethane cycloaddition.

Authors:  Barry M Trost; Dustin A Bringley; Ting Zhang; Nicolai Cramer
Journal:  J Am Chem Soc       Date:  2013-11-06       Impact factor: 15.419

7.  Molecular Basis for Spirocycle Formation in the Paraherquamide Biosynthetic Pathway.

Authors:  Amy E Fraley; Kersti Caddell Haatveit; Ying Ye; Samantha P Kelly; Sean A Newmister; Fengan Yu; Robert M Williams; Janet L Smith; K N Houk; David H Sherman
Journal:  J Am Chem Soc       Date:  2020-01-16       Impact factor: 15.419

8.  Studies on Paraherquamide Biosynthesis: Synthesis of Deuterium-Labeled 7-Hydroxy-Pre-Paraherquamide, a Putative Precursor of Paraherquamides A, E & F.

Authors:  Konrad Sommer; Robert M Williams
Journal:  Tetrahedron       Date:  2009-04-18       Impact factor: 2.457

9.  Paraherquamide e.

Authors:  Thammarat Aree; Bassey S Antia; Okon D Ekpa; Prasat Kittakoop
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2010-08-11

Review 10.  Metabolites from nematophagous fungi and nematicidal natural products from fungi as alternatives for biological control. Part II: metabolites from nematophagous basidiomycetes and non-nematophagous fungi.

Authors:  Thomas Degenkolb; Andreas Vilcinskas
Journal:  Appl Microbiol Biotechnol       Date:  2016-01-04       Impact factor: 4.813

  10 in total

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