Evidence map›Paper›PMID 31028660›Full record

ArticleJournal of natural medicines2019

Three new alkaloids from the roots of Sophora tonkinensis.

Chun Wu, Lijun He, Xue Yi, Juan Qin, Yaolan Li, Yubo Zhang, Guocai Wang

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of natural medicines, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Biological Activities and Secondary Metabolites fromMolecules (Basel, Switzerland) · 2022
    Review
  5. Article
  6. Five matrine-type alkaloids from Sophora tonkinensis.Journal of natural medicines · 2021
    Article
  7. Preparative Purification of Total Flavonoids fromMolecules (Basel, Switzerland) · 2019
    Article
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.

Chun WuXiamen Key Laboratory of Traditional Chinese Medicine Bio-Engineering, Xiamen Medical College, Xiamen, 361023, China.
Lijun HeInstitute of Traditional Chinese Medicine and Natural Products, College of Pharmacy, Jinan University, Guangzhou, 510632, China.
Xue YiKey Laboratory of Functional and Clinical Translational Medicine, Xiamen Medical College, Fujian Province University, Xiamen, 361023, China.
Juan QinInstitute of Traditional Chinese Medicine and Natural Products, College of Pharmacy, Jinan University, Guangzhou, 510632, China.
Yaolan LiInstitute of Traditional Chinese Medicine and Natural Products, College of Pharmacy, Jinan University, Guangzhou, 510632, China.
Yubo ZhangInstitute of Traditional Chinese Medicine and Natural Products, College of Pharmacy, Jinan University, Guangzhou, 510632, China. ybzhang99@126.com.
Guocai WangInstitute of Traditional Chinese Medicine and Natural Products, College of Pharmacy, Jinan University, Guangzhou, 510632, China. twangguocai@jnu.edu.cn.

Funding

China Postdoctoral Science Foundation 2017 M620405Fujian Junior Teachers Education Scientific Research Project Plan JA15812Natural Science Foundation of Guangdong Province 2017A030313732Natural Science Foundations of China 81673319Natural Science Foundations of China 81673670Natural Science Foundations of China 81803376Science and Technology Planning Project of Guangdong Province 2016A030303011Science and Technology Planning Project of Guangdong Province 2016B03030100Science and Technology Planning Project of Guangzhou City 201707010399
6 · The paper itself

Abstract

A new β-carboline alkaloid (1) and two new matrine-type alkaloids (2 and 3), together with two known alkaloids (4 and 5), were isolated from the roots of Sophora tonkinensis. The new structures were elucidated via extensive analyses of the spectroscopic data (IR, UV, HRESIMS, NMR) and X-ray crystallography. The absolute configuration of 1 was established by electronic circular dichroism data. Herein, is the first report of β-carboline alkaloid in the plant of genus Sophora. In addition, the cytotoxic activities against HepG2 cells of compounds 1-5 were evaluated using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay. Among them, compounds 1, 4 and 5 showed a weak cytotoxic activity with IC

Indexed as

AlkaloidsHumansMolecular StructurePlant RootsSophoraAlkaloidsAlkaloidCytotoxic activitySophora tonkinensis

Identifiers

What OpenQuestion holds

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Registered trials

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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.