Literature DB >> 17686499

Insecticidal activity of 12-epi-hapalindole J isonitrile.

Paul G Becher1, Simone Keller, Günther Jung, Roderich D Süssmuth, Friedrich Jüttner.   

Abstract

12-epi-Hapalindole J isonitrile (1) and three previously described hapalindoles, 12-epi-hapalindole C isonitrile (2), hapalindole L (3) and 12-epi-hapalindole E isonitrile (4) were isolated and identified as insecticidal alkaloids of the biofilm-forming freshwater cyanobacterium Fischerella ATCC 43239 (Stigonematales). The structures of the purified compounds were elucidated by ESI-FTICR-MS, GC-EI-MS and various 2D NMR experiments. At 26 microM hapalindole 1 killed 100% of the larvae of the dipteran Chironomus riparius within 48h. Insecticidal activities were also found at similar concentration for the hapalindoles 2-4. The bioactivity of hapalindoles demonstrates that cyanobacterial biofilms can be considered as promising sources of insecticidal metabolites which might be useful for the biocontrol of dipterans.

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Year:  2007        PMID: 17686499     DOI: 10.1016/j.phytochem.2007.06.024

Source DB:  PubMed          Journal:  Phytochemistry        ISSN: 0031-9422            Impact factor:   4.072


  15 in total

1.  Enantiospecific total synthesis of the hapalindoles, fischerindoles, and welwitindolinones via a redox economic approach.

Authors:  Jeremy M Richter; Yoshihiro Ishihara; Takeshi Masuda; Brandon W Whitefield; Tomás Llamas; Antti Pohjakallio; Phil S Baran
Journal:  J Am Chem Soc       Date:  2008-12-31       Impact factor: 15.419

2.  Nitrile-Containing Fischerindoles from the Cultured Cyanobacterium Fischerella sp.

Authors:  Hyunjung Kim; Aleksej Krunic; Daniel Lantvit; Qi Shen; David J Kroll; Steven M Swanson; Jimmy Orjala
Journal:  Tetrahedron       Date:  2012-04-15       Impact factor: 2.457

3.  Hapalindole/Ambiguine Biogenesis Is Mediated by a Cope Rearrangement, C-C Bond-Forming Cascade.

Authors:  Shasha Li; Andrew N Lowell; Fengan Yu; Avi Raveh; Sean A Newmister; Nathan Bair; Jeffrey M Schaub; Robert M Williams; David H Sherman
Journal:  J Am Chem Soc       Date:  2015-12-02       Impact factor: 15.419

4.  Structural basis of the Cope rearrangement and cyclization in hapalindole biogenesis.

Authors:  Sean A Newmister; Shasha Li; Marc Garcia-Borràs; Jacob N Sanders; Song Yang; Andrew N Lowell; Fengan Yu; Janet L Smith; Robert M Williams; K N Houk; David H Sherman
Journal:  Nat Chem Biol       Date:  2018-03-12       Impact factor: 15.040

Review 5.  The chemical ecology of cyanobacteria.

Authors:  Pedro N Leão; Niclas Engene; Agostinho Antunes; William H Gerwick; Vitor Vasconcelos
Journal:  Nat Prod Rep       Date:  2012-01-12       Impact factor: 13.423

6.  Scalable Total Syntheses of (-)-Hapalindole U and (+)-Ambiguine H.

Authors:  Thomas J Maimone; Yoshihiro Ishihara; Phil S Baran
Journal:  Tetrahedron       Date:  2015-05-02       Impact factor: 2.457

7.  Total Synthesis of Pentacyclic (-)-Ambiguine P Using Sequential Indole Functionalizations.

Authors:  Rebecca E Johnson; Hwisoo Ree; Marco Hartmann; Laura Lang; Shota Sawano; Richmond Sarpong
Journal:  J Am Chem Soc       Date:  2019-02-04       Impact factor: 15.419

8.  Indole alkaloids from two cultured cyanobacteria, Westiellopsis sp. and Fischerella muscicola.

Authors:  Hyunjung Kim; Daniel Lantvit; Chang Hwa Hwang; David J Kroll; Steven M Swanson; Scott G Franzblau; Jimmy Orjala
Journal:  Bioorg Med Chem       Date:  2012-07-05       Impact factor: 3.641

9.  Antifeedant, larvicidal and growth inhibitory bioactivities of novel polyketide metabolite isolated from Streptomyces sp. AP-123 against Helicoverpa armigera and Spodoptera litura.

Authors:  Mariadhas Valan Arasu; Naif Abdullah Al-Dhabi; Valsalam Saritha; Veeramuthu Duraipandiyan; Chinnasamy Muthukumar; Sun-Ju Kim
Journal:  BMC Microbiol       Date:  2013-05-13       Impact factor: 3.605

Review 10.  Recent advances in hapalindole-type cyanobacterial alkaloids: biosynthesis, synthesis, and biological activity.

Authors:  Robert M Hohlman; David H Sherman
Journal:  Nat Prod Rep       Date:  2021-09-23       Impact factor: 15.111

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