Evidence map›Paper›PMID 42763914›Full record

ArticleChemistry & biodiversity2026

Anti‑Inflammatory Sesquiterpenoids From Two Asteraceae Plants Native to Kazakhstan: Isolation, Structural Elucidation, and Mechanistic Insights.

Arailym Zhomartova, Wen-Jing Gao, Janar Jenis, Chu-Hong Fang, Pei-Qian Wu, Jian-Min Yue, Bin Zhou

Abstract read
In one paragraph

Article in Chemistry & biodiversity, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Arailym Zhomartova *Ethnomedicine and Biofunctional Molecule Research Center, State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, China.
Wen-Jing Gao *Shandong Laboratory of Yantai Drug Discovery, Bohai Rim Advanced Research Institute for Drug Discovery, Yantai, Shandong, Republic of China.
Janar JenisThe Research Center for Medicinal Plants, Al-Farabi Kazakh National University, Almaty, Kazakhstan.
Chu-Hong FangShandong Laboratory of Yantai Drug Discovery, Bohai Rim Advanced Research Institute for Drug Discovery, Yantai, Shandong, Republic of China.
Pei-Qian WuEthnomedicine and Biofunctional Molecule Research Center, State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, China.
Jian-Min YueEthnomedicine and Biofunctional Molecule Research Center, State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, China.ORCID https://orcid.org/0000-0002-4053-4870
Bin ZhouEthnomedicine and Biofunctional Molecule Research Center, State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, China.ORCID https://orcid.org/0000-0001-9000-5320

Funding

National Natural Science Foundation of China 22494691National Natural Science Foundation of China 82322064
6 · The paper itself

Abstract

Traditionally used in Kazakh folk medicine, the Asteraceae species Taraxacum tianschanicum and Artemisia gracilescens were investigated for their sesquiterpenoid profiles despite being rich in flavonoids and fatty acids, leading to the isolation of 10 sesquiterpenoids of three structural types. These include one previously undescribed germacrane (1) and two known germacranes (2 and 3) from T. tianschanicum, as well as two germacranes (4 and 5), one guaiane (6), and four eudesmanes (7-10) from A. gracilescens. The structures of these compounds were established through comprehensive analysis of the spectroscopic data and electronic circular dichroism (ECD) calculations. Several compounds exhibited significant anti-inflammatory effects (IC

Indexed as

Anti-Inflammatory AgentsAnti-Inflammatory Agents, Non-SteroidalArtemisiaAsteraceaeSesquiterpenesTaraxacumAnimalsCyclooxygenase 2Dose-Response Relationship, DrugLipopolysaccharidesMiceMolecular ConformationMolecular StructureNitric OxideNitric Oxide Synthase Type IIRAW 264.7 CellsAnti-Inflammatory AgentsAnti-Inflammatory Agents, Non-SteroidalCyclooxygenase 2LipopolysaccharidesNitric OxideNitric Oxide Synthase Type IISesquiterpenesanti‐inflammationArtemisia gracilescensasteraceaemechanistic studiessesquiterpenoidsTaraxacum tianschanicum

Identifiers

PMID42763914
PMCPMC13590133

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.