Three New Derivatives and Others Constituents from the Roots and Twigs of Trilepisium madagascariense DC
Three new compounds, trilepisflavene (1), trilepisdepsidone (2), and daturadiol stearate (3), together with nine known compounds, 2‐hydroxy‐4‐[(4‐hydroxy‐2‐methoxy‐6‐methylbenzoyl)oxy]‐6‐methylbenzoic acid (4), lichexanthone (5), naringenin (6), 3′,4′,5,7‐tetrahydroxyflavanone (7), 2‐hydroxybenzoic...
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Published in: | Helvetica chimica acta Vol. 99; no. 8; pp. 642 - 649 |
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Main Authors: | , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Zürich
Blackwell Publishing Ltd
01-08-2016
Wiley Subscription Services, Inc |
Subjects: | |
Online Access: | Get full text |
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Summary: | Three new compounds, trilepisflavene (1), trilepisdepsidone (2), and daturadiol stearate (3), together with nine known compounds, 2‐hydroxy‐4‐[(4‐hydroxy‐2‐methoxy‐6‐methylbenzoyl)oxy]‐6‐methylbenzoic acid (4), lichexanthone (5), naringenin (6), 3′,4′,5,7‐tetrahydroxyflavanone (7), 2‐hydroxybenzoic acid (8), methyl 2,4‐dihydroxy‐6‐methylbenzoate (9), β‐amyrin (10), eurothridiol palmitate (11), and β‐sitosterol (12), were isolated from the AcOEt extract of the twigs and the roots of Trilepisium madagascariense. Acetylation of eurothridiol palmitate was carried out and a new acetylated derivative (13) was obtained. The structures of the isolated and acetylated compounds were elucidated on the basis of spectroscopic analysis. Antimicrobial activity of all these compounds was evaluated using Mueller–Hinton broth (MHB) and Mueller–Hinton agar (MHA) method. Trilepisdepsidone, 2‐hydroxy‐4‐[(4‐hydroxy‐2‐methoxy‐6‐methylbenzoyl)oxy]‐6‐methylbenzoic acid, 3′,4′,5,7‐tetrahydroxyflavanone, and naringenin exhibited moderate to weak antimicrobial activity.
Three New Derivatives and Others Constituents from the Roots and Twigs of Trilepisium madagascariense DC
Y. P. Ango, G. D. W. F. Kapche*, V. Kuete, R. Mapitse, S. O. Yeboah, B. T. Ngadjui |
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Bibliography: | ark:/67375/WNG-DQLMD3D2-B Organisation for the Prohibition of Chemical Weapons (OPCW) istex:C7BE60DE7B574D36A88038D29FD09C3BFC046762 ArticleID:HLCA201600073 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0018-019X 1522-2675 |
DOI: | 10.1002/hlca.201600073 |