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

Authors :
Noulala CGT
Ouete JLN
Atangana AF
Mbahbou GTB
Fotso GW
Stammler HG
Lenta BN
Happi EN
Sewald N
Ngadjui BT
Source :
Molecules (Basel, Switzerland) [Molecules] 2022 Feb 07; Vol. 27 (3). Date of Electronic Publication: 2022 Feb 07.
Publication Year :
2022

Abstract

The chemical investigation of the total alkaloid extract (TAE) of the stem bark of Araliopsis soyauxii (Rutaceae) afforded an unreported indolopyridoquinazoline (compound 1 ) along with nine previously known alkaloids 2 - 10 . In addition, six semi-synthetic derivatives 3a - c , 4b , 5a and 6a were prepared by allylation and acetonidation of soyauxinium nitrate ( 5 ), edulinine ( 3 ), ribalinine ( 4 ) and arborinine ( 6 ). 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 N -allylindolopyridoquinazoline 5a 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 2 - 4 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 ( 5 ). The TAE, fractions, compounds 1 - 7 and 9 , and semi-synthetic derivatives 3a - c , 4b , 5a and 6a 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 9 , which showed moderate activity against the tested cancer cell lines.

Details

Language :
English
ISSN :
1420-3049
Volume :
27
Issue :
3
Database :
MEDLINE
Journal :
Molecules (Basel, Switzerland)
Publication Type :
Academic Journal
Accession number :
35164367
Full Text :
https://doi.org/10.3390/molecules27031104