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Iboga-type alkaloids from the leaves of Tabernaemontana penduliflora (Apocynaceae).

Authors :
Nama, Alexis Bienvenue
Paululat, Thomas
Ebede, Guy Roland
Betote, Patrick Hervé Diboue
Pegnyemb, Dieudonné Emmanuel
Mbing, Joséphine Ngo
Ndongo, Joseph Thierry
Ihmels, Heiko
Laatsch, Hartmut
Source :
Phytochemistry Letters; Apr2023, Vol. 54, p63-69, 7p
Publication Year :
2023

Abstract

Isolation studies on the leaves of Tabernaemontana penduliflora afforded two undescribed indole alkaloids, 7,10-dihydroxyindolenine (1a) and pendulifloramine (2), together with four known compounds, 10-hydroxyheyneanine (4), 10-hydroxycoronaridine (5), vobasine (6), and voacristine (7). The structures 1a and 2 were determined based on NMR and mass spectra, together with database mining and computer-assisted structure elucidation. Their absolute and relative configurations were deduced by comparison of their CD spectra with those of known compounds and of the ab initio calculated spectra. Compounds 1a and 2 displayed moderate radical-trapping activity towards 2,2-diphenyl-1-picrylhydrazyl (DPPH) with 50 % scavenging capacity activity (SC 50) values of 34 µg/mL and 46 µg/mL, respectively, and good ability to reduce the TPTZ-Fe(III) complex to TPTZ-Fe(II) (TPTZ = 2,4,6-Tri-(2-pyridyl)- s -triazin) with 133 µg EGA/mg and 186 µg EGA/mg of dry weight, respectively. Both compounds also have anti-inflammatory activity with IC 50 values of 9 µg/mL and 5 µg/mL for 1a and 2 , respectively. [Display omitted] • Phytochemical studies have been done on the leaves of Tabernaemontana penduliflora. • Two new compounds (1a - 2) were isolated from the enriched alkaloids extract. • Compounds 1a and 2 showed anti-inflammatory activity and antioxidative properties. • The IC 50 values of compounds 1a and 2 were 9 µg/mL and 5 µg/mL, respectively. • The SC 50 values were 133 µg EGA/mg and 186 µg EGA/mg, respectively. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
18743900
Volume :
54
Database :
Supplemental Index
Journal :
Phytochemistry Letters
Publication Type :
Academic Journal
Accession number :
162475782
Full Text :
https://doi.org/10.1016/j.phytol.2023.01.018