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Paecilosetin Derivatives as Potent Antimicrobial Agents from Isaria farinosa.
Brel, Orianne; Touré, Seindé; Levasseur, Marceau; Lechat, Christian; Pellissier, Léonie; Wolfender, Jean-Luc; Van-Elslande, Elsa; Litaudon, Marc; Dusfour, Isabelle; Stien, Didier; Eparvier, Véronique.
Afiliação
  • Brel O; Université Paris-Saclay, CNRS, Institut de Chimie des Substances Naturelles, UPR 2301, 91198, Gif-sur-Yvette, France.
  • Touré S; Université Paris-Saclay, CNRS, Institut de Chimie des Substances Naturelles, UPR 2301, 91198, Gif-sur-Yvette, France.
  • Levasseur M; Université Paris-Saclay, CNRS, Institut de Chimie des Substances Naturelles, UPR 2301, 91198, Gif-sur-Yvette, France.
  • Lechat C; ASCOFrance, 79360, Villiers-en-bois, France.
  • Pellissier L; School of Pharmaceutical Sciences, University of Geneva, CMU, 1211 Geneva 4, Switzerland.
  • Wolfender JL; Institute of Pharmaceutical Sciences of Western Switzerland, University of Geneva, CMU, CH-1211 Geneva 4, Switzerland.
  • Van-Elslande E; School of Pharmaceutical Sciences, University of Geneva, CMU, 1211 Geneva 4, Switzerland.
  • Litaudon M; Institute of Pharmaceutical Sciences of Western Switzerland, University of Geneva, CMU, CH-1211 Geneva 4, Switzerland.
  • Dusfour I; Université Paris-Saclay, CNRS, Institut de Chimie des Substances Naturelles, UPR 2301, 91198, Gif-sur-Yvette, France.
  • Stien D; Université Paris-Saclay, CNRS, Institut de Chimie des Substances Naturelles, UPR 2301, 91198, Gif-sur-Yvette, France.
  • Eparvier V; Institut Pasteur de la Guyane, Unité de Contrôle et Adaptation des Vecteurs, BP6010, 97306 Cayenne, France.
J Nat Prod ; 83(10): 2915-2922, 2020 10 23.
Article em En | MEDLINE | ID: mdl-33021377
ABSTRACT
Fifty-seven entomopathogenic microorganisms were screened against human pathogens and subjected to mass spectrometry molecular networking based dereplication. Isaria farinosa BSNB-1250, shown to produce potentially novel biologically active metabolites, was grown on a large scale on potato dextrose agar, and paecilosetin (1) and five new analogues (2-6) were subsequently isolated. The structures of the new compounds were elucidated using 1D and 2D NMR. The absolute configurations of compounds 1-6 were determined using Mosher ester derivatives (1, 3, 4), comparison of experimental and calculated ECD spectra (2-4 and 6), and single-crystal X-ray diffraction analysis (5). Compounds 1 and 5 exhibited strong antibacterial activity against MSSA and MRSA with MIC values of 1-2 µg/mL.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pirrolidinonas / Cordyceps / Anti-Infecciosos Limite: Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pirrolidinonas / Cordyceps / Anti-Infecciosos Limite: Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article