Ferlapioside: a new bromine substituted iridoid glycoside from the roots of <i>Ferula lapidosa</i> Korovin

One new bromine substituted iridoid glycoside, ferlapioside (<b>1</b>), was isolated from the roots of <i>Ferula lapidosa</i> Korovin, together with 10 known ones including seven iridoid glycosides (<b>2</b>-<b>8</b>) and three sesquiterpene lactones (<b>9</b>-<b>11</b>). Their structures were elucidated by extensive spectroscopic analyses, e.g. 1D and 2D-NMR, HR-ESI-MS, IR, UV, CD techniques, and comparison with literature values. Compounds <b>1</b> and <b>3</b>-<b>11</b> were evaluated for inhibitory activity against LPS-induced NO production in the RAW 264.7 cells and the <i>in vitro</i> cytotoxic activity against five human cancer cell lines (HL-60, A549, SMMC-7721, MDA-MB-231 and SW480). However, none of them exhibit significant anti-inflammatory and cytotoxic activity. This study will provide a scientific basis and reference for the further development and utilisation of <i>Ferula</i> plants.

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Publication Details

Journal
Natural Product Research
Published
2024-12-01
DOI
https://doi.org/10.1080/14786419.2024.2432613
Primary Topic
Plant chemical constituents analysis
Type
article
Field-Weighted Citation Impact
0.00

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article

Ferlapioside: a new bromine substituted iridoid glycoside from the roots of Ferula lapidosa Korovin

Kholida Khasanova, K. A. Éshbakova, Anarbay Babekov, Jia-Huan Shang et al.
Natural Product Research
Plant chemical constituents analysis
article

Ferlapioside: a new bromine substituted iridoid glycoside from the roots of Ferula lapidosa Korovin

Kholida Khasanova, K. A. Éshbakova, Anarbay Babekov, Jia-Huan Shang, Jingjuan Li, Wen‐Jun Li, Ying‐Jun Zhang, Hongtao Zhu, Xinxin Li
article en

Abstract

One new bromine substituted iridoid glycoside, ferlapioside (<b>1</b>), was isolated from the roots of <i>Ferula lapidosa</i> Korovin, together with 10 known ones including seven iridoid glycosides (<b>2</b>-<b>8</b>) and three sesquiterpene lactones (<b>9</b>-<b>11</b>). Their structures were elucidated by extensive spectroscopic analyses, e.g. 1D and 2D-NMR, HR-ESI-MS, IR, UV, CD techniques, and comparison with literature values. Compounds <b>1</b> and <b>3</b>-<b>11</b> were evaluated for inhibitory activity against LPS-induced NO production in the RAW 264.7 cells and the <i>in vitro</i> cytotoxic activity against five human cancer cell lines (HL-60, A549, SMMC-7721, MDA-MB-231 and SW480). However, none of them exhibit significant anti-inflammatory and cytotoxic activity. This study will provide a scientific basis and reference for the further development and utilisation of <i>Ferula</i> plants.

Natural Product ResearchVol. 40(7)
Kunming Institute of Botany (CN), Osh State University (KG), Chinese Academy of Sciences (CN), Xinjiang Production and Construction Corps (CN), Tashkent Institute of Irrigation and Agricultural Mechanization Engineers (UZ), Yunusov Institute of the Chemistry of Plant Substances (UZ), University of Chinese Academy of Sciences (CN)
National Natural Science Foundation of China
Zero hunger
Openalex Percentile: Top 88%
Plant chemical constituents analysis
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