Ferusamarbiclins A−C and Ferusamarelemanolide A, Sesquiterpenes from the Roots of Ferula samarkandica

Abstract Four sesquiterpenes with previously undescribed backbones, named ferusamarbiclins A−C (1−3) and ferusamarelemanolide A (4), were isolated from the roots of Ferula samarkandica. Structurally, ferusamarbiclins A−C shared a 4-methyl-7-isopropyl-bicyclo[5.3.1]undecane-type sesquiterpene scaffold termed ferusamarbiclane, closely related to germacrane-type sesquiterpenoids in terms of origin. Ferusamarelemanolide A represented a 6,7-seco-elemane-type sesquiterpene lactone with the architecture designated ferusamarelemane. Their structures were established on the basis of comprehensive spectroscopic analysis, including HRESIMS, NMR, UV, and IR. The absolute configurations were determined by ECD calculations combined with single-crystal X-ray diffraction crystallography. Furthermore, plausible biosynthetic pathways were proposed. Compounds 1−4 displayed a weak antimicrobial activity against Candida albicans and Staphylococcus aureus.

Authors

Institutions

Publication Details

Journal
Journal of Natural Products
Published
2026-10-29
DOI
https://doi.org/10.1021/acs.jnatprod.6c01013
Primary Topic
Sesquiterpenes and Asteraceae Studies
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Ferusamarbiclins A−C and Ferusamarelemanolide A, Sesquiterpenes from the Roots of Ferula samarkandica

Haji Akber Aisa, Khamidulla Kamoldinov, Haiqing Zhao, Guo‐An Zou et al.
1 links
Journal of Natural Products
Sesquiterpenes and Asteraceae Studies
article

Ferusamarbiclins A−C and Ferusamarelemanolide A, Sesquiterpenes from the Roots of Ferula samarkandica

Haji Akber Aisa, Khamidulla Kamoldinov, Haiqing Zhao, Guo‐An Zou, Yuqing Song, Defeng Yan, Miaomiao Zhang
article en

Abstract

Abstract Four sesquiterpenes with previously undescribed backbones, named ferusamarbiclins A−C (1−3) and ferusamarelemanolide A (4), were isolated from the roots of Ferula samarkandica. Structurally, ferusamarbiclins A−C shared a 4-methyl-7-isopropyl-bicyclo[5.3.1]undecane-type sesquiterpene scaffold termed ferusamarbiclane, closely related to germacrane-type sesquiterpenoids in terms of origin. Ferusamarelemanolide A represented a 6,7-seco-elemane-type sesquiterpene lactone with the architecture designated ferusamarelemane. Their structures were established on the basis of comprehensive spectroscopic analysis, including HRESIMS, NMR, UV, and IR. The absolute configurations were determined by ECD calculations combined with single-crystal X-ray diffraction crystallography. Furthermore, plausible biosynthetic pathways were proposed. Compounds 1−4 displayed a weak antimicrobial activity against Candida albicans and Staphylococcus aureus.

Journal of Natural Products
Chinese Academy of Sciences (CN), Namangan Engineering Pedagogical Institute (UZ), University of Chinese Academy of Sciences (CN), Namangan Institute of Engineering and Technology (UZ)
Chinese Academy of Sciences, West Light Foundation of the Chinese Academy of Sciences
Openalex Percentile: Top 17%
Sesquiterpenes and Asteraceae Studies
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Laika access coming soon
Ferusamarbiclins A−C and Ferusamarelemanolide A, Sesquiterpenes from the Roots of Ferula samarkandica — Haji Akber Aisa, Khamidulla Kamoldinov, et al. · Journal of Natural Products (2026) | TGRS Research Map | TGRS