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Manniindole, an indole derivative from the roots of Anonidium mannii and combined antischistosomal and enzymatic activities

Authors :
Josette Linda Toussi Matchi
Marc Nothisen
Jean Claude Tchouankeu
Jérôme Boissier
Sylvain Ursuegui
Guilhem Chaubet
Silvère Ngouela
Delphine Garnier
Diderot T. Noungoue
Isabelle Kuhn
Alain Wagner
Conception et application de molécules bioactives (CAMB)
Université de Strasbourg (UNISTRA)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)
Université de Yaoundé I
Interactions Hôtes-Pathogènes-Environnements (IHPE)
Centre National de la Recherche Scientifique (CNRS)-Université de Montpellier (UM)-Institut Français de Recherche pour l'Exploitation de la Mer (IFREMER)-Université de Perpignan Via Domitia (UPVD)
University of Yaounde I, Dept Chim Inorgan, Lab Physicochim Mat Min, Yaounde, Cameroon
Centre National de la Recherche Scientifique (CNRS)-Université de Strasbourg (UNISTRA)
Université de Strasbourg (UNISTRA)-Centre National de la Recherche Scientifique (CNRS)
Source :
Natural Product Research, Natural Product Research, Taylor & Francis, In press, ⟨10.1080/14786419.2020.1824227⟩, Natural Product Research, Taylor & Francis, 2020, pp.1-9. ⟨10.1080/14786419.2020.1824227⟩, Natural Product Research (1478-6419) (Taylor & Francis Ltd), 2021-12, Vol. 35, N. 24, P. 5665-5673
Publication Year :
2021
Publisher :
HAL CCSD, 2021.

Abstract

International audience; A new alkaloid, manniindole 1, together with four known compounds: aristolactam AII 2, aristolactam BII 3, piperolactam D 4 and polycarpol 5 were isolated from the crude extract EtOHH2O (8:2) of the roots of Anonidium mannii by chromatographic separation. The structure elucidation was performed on the basis of a spectroscopic analysis (IR, HRESI MS, 1D and 2D NMR) as well as a comparison of their spectral data with those reported in the literature. For the first time, the crude extract and those isolated compounds were evaluated for their antischistosomal activity against Schistosoma mansoni and for cytotoxicity activity against Huh7 and A549 cells. Furthermore, they were also tested in vitro on the recent characterized Schistosoma mansoni NADþ catabolizing enzyme (SmNACE) for their impact on this enzyme which is localized on the outer surface of the adult parasite. Compound 2 displayed quite good worm killing capability, while 4 showed significant inhibition of SmNACE

Details

Language :
English
ISSN :
14786419 and 10292349
Database :
OpenAIRE
Journal :
Natural Product Research, Natural Product Research, Taylor & Francis, In press, ⟨10.1080/14786419.2020.1824227⟩, Natural Product Research, Taylor & Francis, 2020, pp.1-9. ⟨10.1080/14786419.2020.1824227⟩, Natural Product Research (1478-6419) (Taylor & Francis Ltd), 2021-12, Vol. 35, N. 24, P. 5665-5673
Accession number :
edsair.doi.dedup.....87574a5438ef0c378d46a04782b6d564
Full Text :
https://doi.org/10.1080/14786419.2020.1824227⟩