Planta Med 2019; 85(11/12): 947-956
DOI: 10.1055/a-0941-0364
Biological and Pharmacological Activities
Original Papers
Georg Thieme Verlag KG Stuttgart · New York

Guaianolides from Ormenis mixta: Structural Insights and Evaluation of Their Anti-inflammatory Profile[*]

Authors

  • Mounira Benteldjoune

    1   Laboratoire DʼObtention des Substances Thérapeutiques (LOST), Département de Chimie, Université des Frères Mentouri-Constantine, Constantine, Algeria
  • Maria Giovanna Chini

    2   Dipartimento di Farmacia, Università di Salerno, Fisciano (SA), Italy
  • Anna Maria Iannuzzi

    3   Dipartimento di Farmacia, Università di Pisa, Pisa, Italy
  • Ahmed Kabouche

    1   Laboratoire DʼObtention des Substances Thérapeutiques (LOST), Département de Chimie, Université des Frères Mentouri-Constantine, Constantine, Algeria
  • Zahia Kabouche

    1   Laboratoire DʼObtention des Substances Thérapeutiques (LOST), Département de Chimie, Université des Frères Mentouri-Constantine, Constantine, Algeria
  • Massimiliano DʼAmbola

    2   Dipartimento di Farmacia, Università di Salerno, Fisciano (SA), Italy
  • Stefania Marzocco

    2   Dipartimento di Farmacia, Università di Salerno, Fisciano (SA), Italy
  • Giuseppina Autore

    2   Dipartimento di Farmacia, Università di Salerno, Fisciano (SA), Italy
  • Giuseppe Bifulco

    2   Dipartimento di Farmacia, Università di Salerno, Fisciano (SA), Italy
  • Nunziatina De Tommasi

    2   Dipartimento di Farmacia, Università di Salerno, Fisciano (SA), Italy
Weitere Informationen

Publikationsverlauf

received 19. Februar 2019
revised 15. Mai 2019

accepted 20. Mai 2019

Publikationsdatum:
04. Juni 2019 (online)

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Abstract

In this paper, the isolation of five new guaianolides (1 – 5) and four (6 – 9) known sesquiterpenes from Ormenis mixta aerial parts is reported. The structural determination of the guaianolides was obtained by NMR spectroscopic data, as well as MS experiments. Their relative configurations were assigned by a combined quantum mechanical/NMR approach, comparing the experimental 13C/1H NMR chemical shift data and 1 J H-H homonuclear coupling constants with the related predicted values. The isolates were assayed for their anti-inflammatory potential evaluating nitric oxide release and cyclooxygenase-2 expression in J774A.1 macrophages treated with lipopolysaccharide from Escherichia coli. Our results indicated that, among the tested compounds, 1 – 3, and 7 were able to inhibit nitric oxide release, while all were able to inhibit cyclooxygenase-2 expression with different potencies.

* Dedicated to Professor Dr. Cosimo Pizza 70th birthday in recognition of his outstanding contribution to natural product research.


Supporting Information