Soyauxinine, a New Indolopyridoquinazoline Alkaloid from the Stem Bark of Araliopsis soyauxii Engl. (Rutaceae)

The chemical investigation of the total alkaloid extract (TAE) of the stem bark of (Rutaceae) afforded an unreported indolopyridoquinazoline (compound ) along with nine previously known alkaloids - . In addition, six semi-synthetic derivatives - , , and were prepared by allylation and acetonidation...

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Veröffentlicht in:Molecules (Basel, Switzerland) Switzerland), 2022-02, Vol.27 (3), p.1104
Hauptverfasser: Noulala, Cédric Guy Tchatchouang, Ouete, Judith Laure Nantchouang, Atangana, Albert Fouda, Mbahbou, Gabin Thierry Bitchagno, Fotso, Ghislain Wabo, Stammler, Hans-Georg, Lenta, Bruno Ndjakou, Happi, Emmanuel Ngeufa, Sewald, Norbert, Ngadjui, Bonaventure Tchaleu
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Sprache:eng
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Zusammenfassung:The chemical investigation of the total alkaloid extract (TAE) of the stem bark of (Rutaceae) afforded an unreported indolopyridoquinazoline (compound ) along with nine previously known alkaloids - . In addition, six semi-synthetic derivatives - , , and were prepared by allylation and acetonidation of soyauxinium nitrate ( ), edulinine ( ), ribalinine ( ) and arborinine ( ). The structures and spectroscopic data of five of them are reported herein for the first time. The suggested mechanism for the formation of the new -allylindolopyridoquinazoline is presented. The structures of natural and derived compounds were determined employing extensive NMR and MS techniques. The absolute configuration of stereogenic centers in compounds - were determined using NOESY technique and confirmed by the single-crystal X-ray diffraction (SC-XRD) technique. The use of SC-XRD further enabled us to carry out a structural revision of soyauxinium chloride recently isolated from the same plant to soyauxinium nitrate ( ). The TAE, fractions, compounds - and , and semi-synthetic derivatives - , , and were evaluated for their cytotoxic activity towards the cervix carcinoma cell line KB-3-1. No significant activity was recorded for most of the compounds except for , which showed moderate activity against the tested cancer cell lines.
ISSN:1420-3049
1420-3049
DOI:10.3390/molecules27031104