Lepiginosides A-D: three new triterpenoid saponins and a new farnesyl glycoside from the stembarks of Lepisanthes rubiginosa (roxb.) leenh

Lepiginosides A-D: three new triterpenoid saponins and a new farnesyl glycoside from the stembarks of Lepisanthes rubiginosa (roxb.) leenh

Phytochemical investigation of methanolic extract of L. rubiginosa using modern chromatographic techniques has led to the isolation of three new triterpenoid saponins, lepiginosides A-C (1-3), a new farnesyl glycoside, lepiginoside D (4), together with lepisantheside B (5) and gleditsoside C (6). Th...

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Published in:Natural Product Research
Main Author: Zulkifli S.Z.; Ab Ghani N.; Rasol N.E.; Salleh W.M.N.H.W.; Ismail N.H.
Format: Article
Language:English
Published: Taylor and Francis Ltd. 2024
Online Access:https://www.scopus.com/inward/record.uri?eid=2-s2.0-85134525104&doi=10.1080%2f14786419.2022.2102629&partnerID=40&md5=f29b804538e878333be1f3b39a434b5a
id 2-s2.0-85134525104
spelling 2-s2.0-85134525104
Zulkifli S.Z.; Ab Ghani N.; Rasol N.E.; Salleh W.M.N.H.W.; Ismail N.H.
Lepiginosides A-D: three new triterpenoid saponins and a new farnesyl glycoside from the stembarks of Lepisanthes rubiginosa (roxb.) leenh
2024
Natural Product Research
38
1
10.1080/14786419.2022.2102629
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85134525104&doi=10.1080%2f14786419.2022.2102629&partnerID=40&md5=f29b804538e878333be1f3b39a434b5a
Phytochemical investigation of methanolic extract of L. rubiginosa using modern chromatographic techniques has led to the isolation of three new triterpenoid saponins, lepiginosides A-C (1-3), a new farnesyl glycoside, lepiginoside D (4), together with lepisantheside B (5) and gleditsoside C (6). The characterization and structural elucidation of the isolated compounds were established by extensive spectroscopic data analysis and comparison with literature data. Moreover, the antibacterial activity against seven bacteria, but none is active. © 2022 Informa UK Limited, trading as Taylor & Francis Group.
Taylor and Francis Ltd.
14786419
English
Article
author Zulkifli S.Z.; Ab Ghani N.; Rasol N.E.; Salleh W.M.N.H.W.; Ismail N.H.
spellingShingle Zulkifli S.Z.; Ab Ghani N.; Rasol N.E.; Salleh W.M.N.H.W.; Ismail N.H.
Lepiginosides A-D: three new triterpenoid saponins and a new farnesyl glycoside from the stembarks of Lepisanthes rubiginosa (roxb.) leenh
author_facet Zulkifli S.Z.; Ab Ghani N.; Rasol N.E.; Salleh W.M.N.H.W.; Ismail N.H.
author_sort Zulkifli S.Z.; Ab Ghani N.; Rasol N.E.; Salleh W.M.N.H.W.; Ismail N.H.
title Lepiginosides A-D: three new triterpenoid saponins and a new farnesyl glycoside from the stembarks of Lepisanthes rubiginosa (roxb.) leenh
title_short Lepiginosides A-D: three new triterpenoid saponins and a new farnesyl glycoside from the stembarks of Lepisanthes rubiginosa (roxb.) leenh
title_full Lepiginosides A-D: three new triterpenoid saponins and a new farnesyl glycoside from the stembarks of Lepisanthes rubiginosa (roxb.) leenh
title_fullStr Lepiginosides A-D: three new triterpenoid saponins and a new farnesyl glycoside from the stembarks of Lepisanthes rubiginosa (roxb.) leenh
title_full_unstemmed Lepiginosides A-D: three new triterpenoid saponins and a new farnesyl glycoside from the stembarks of Lepisanthes rubiginosa (roxb.) leenh
title_sort Lepiginosides A-D: three new triterpenoid saponins and a new farnesyl glycoside from the stembarks of Lepisanthes rubiginosa (roxb.) leenh
publishDate 2024
container_title Natural Product Research
container_volume 38
container_issue 1
doi_str_mv 10.1080/14786419.2022.2102629
url https://www.scopus.com/inward/record.uri?eid=2-s2.0-85134525104&doi=10.1080%2f14786419.2022.2102629&partnerID=40&md5=f29b804538e878333be1f3b39a434b5a
description Phytochemical investigation of methanolic extract of L. rubiginosa using modern chromatographic techniques has led to the isolation of three new triterpenoid saponins, lepiginosides A-C (1-3), a new farnesyl glycoside, lepiginoside D (4), together with lepisantheside B (5) and gleditsoside C (6). The characterization and structural elucidation of the isolated compounds were established by extensive spectroscopic data analysis and comparison with literature data. Moreover, the antibacterial activity against seven bacteria, but none is active. © 2022 Informa UK Limited, trading as Taylor & Francis Group.
publisher Taylor and Francis Ltd.
issn 14786419
language English
format Article
accesstype
record_format scopus
collection Scopus
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