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Dactylfungins and Tetralones: Bioactive Metabolites from a Nematode-Associated Laburnicola nematophila.
Wennrich, Jan-Peer; Holzenkamp, Caren; Kolarík, Miroslav; Maier, Wolfgang; Mándi, Attila; Kurtán, Tibor; Ashrafi, Samad; Ebada, Sherif S; Stadler, Marc.
Afiliación
  • Wennrich JP; Department of Microbial Drugs, Helmholtz Centre for Infection Research (HZI) and German Centre for Infection Research, Inhoffenstrasse 7, 38124 Braunschweig, Germany.
  • Holzenkamp C; Institute of Microbiology, Technische Universität Braunschweig, Spielmannstraße 7, 38106 Braunschweig, Germany.
  • Kolarík M; Department of Microbial Drugs, Helmholtz Centre for Infection Research (HZI) and German Centre for Infection Research, Inhoffenstrasse 7, 38124 Braunschweig, Germany.
  • Maier W; Institute of Microbiology, Technische Universität Braunschweig, Spielmannstraße 7, 38106 Braunschweig, Germany.
  • Mándi A; Institute of Microbiology, Czech Academy of Science, Vídenská 1083, 14220 Prague, Czech Republic.
  • Kurtán T; Institute for Epidemiology and Pathogen Diagonstics, Julius Kühn Institut (JKI) - Federal Research Centre for Cultivated Plants, Messeweg 11-12, 38104 Braunschweig, Germany.
  • Ashrafi S; Department of Organic Chemistry, University of Debrecen, P.O. Box 400, 4002 Debrecen, Hungary.
  • Ebada SS; Department of Organic Chemistry, University of Debrecen, P.O. Box 400, 4002 Debrecen, Hungary.
  • Stadler M; Institute for Epidemiology and Pathogen Diagonstics, Julius Kühn Institut (JKI) - Federal Research Centre for Cultivated Plants, Messeweg 11-12, 38104 Braunschweig, Germany.
J Nat Prod ; 87(7): 1860-1871, 2024 Jul 26.
Article en En | MEDLINE | ID: mdl-39012621
ABSTRACT
A chemical investigation of Laburnicola nematophila, isolated from cysts of the plant parasitic nematode Heterodera filipjevi, affored three dactylfungin derivatives (1-3) and three tetralone congeners (4-6). Dactylfungin C (1), laburnicolin (4), and laburnicolenone (5) are previously undescribed natural products. Chemical structures of the isolated compounds were determined based on 1D and 2D NMR spectroscopic analyses together with HR-ESI-MS spectrometry and comparison with data reported in the literature. The relative configurations of compounds 1, 2, and 4-6 were determined based on their ROESY data and analysis of their coupling constants (J values). The absolute configurations of 4-6 were determined through the comparison of their measured and calculated TDDFT-ECD spectra. Compounds 1-3 were active against azole-resistant Aspergillus fumigatus.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Tetralonas Límite: Animals Idioma: En Revista: J Nat Prod Año: 2024 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Tetralonas Límite: Animals Idioma: En Revista: J Nat Prod Año: 2024 Tipo del documento: Article País de afiliación: Alemania
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