Evidence map›Paper›PMID 41023382›Full record

ArticleScientific reports2025

Investigating C

Taibai Jiang, Lihong Shi, Xueke Peng, Shan Zheng, Qian Chen, Junjie Lan, Weidong Pan

Abstract read
In one paragraph

Article in Scientific reports, 2025. 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
–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

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.

Taibai Jiang *Guizhou Province Engineering Research Center of Medical Resourceful Healthcare Products, College of Pharmacy, Guiyang Healthcare Vocational University, Guiyang, 550081, People's Republic of China.
Lihong Shi *Guizhou Province Engineering Research Center of Medical Resourceful Healthcare Products, College of Pharmacy, Guiyang Healthcare Vocational University, Guiyang, 550081, People's Republic of China.
Xueke PengGuizhou Province Engineering Research Center of Medical Resourceful Healthcare Products, College of Pharmacy, Guiyang Healthcare Vocational University, Guiyang, 550081, People's Republic of China.
Shan ZhengGuizhou Province Engineering Research Center of Medical Resourceful Healthcare Products, College of Pharmacy, Guiyang Healthcare Vocational University, Guiyang, 550081, People's Republic of China.
Qian ChenEugenics Research Center, The First Affiliated Hospital of Guizhou University of Traditional Chinese Medicine, Guiyang, 550002, People's Republic of China.
Junjie LanDepartment of Pharmacy, Guizhou Provincial People's Hospital, Guiyang, 550002, People's Republic of China. lanjunjie2007@163.com.
Weidong PanSchool of Pharmaceutical Sciences, Guizhou University, Guiyang, 550025, People's Republic of China. wdpan@163.com.

Funding

Guizhou Provincial Administration of Traditional Chinese Medicine and Ethnic Medicine Science and Technology Research Project QZYY-2025-086Guizhou Provincial Basic Research Program (Natural Science) QKHJC MS〔2025〕516Guizhou Science and Technology Department ZK [2022]459National Natural Science Foundation of China 81960635Scientific Research Foundation of Guiyang Healthcare Vocational University Guikangda K2024-5Scientific Research Foundation of Guiyang Healthcare Vocational University Guikangda K2024-9
6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) remains a significant global health challenge, with drug therapy being a critical treatment approach. However, the development of drug resistance and the occurrence of adverse reactions to existing medications have made the creation of new HCC treatments urgent. Tetrandrine, a bisbenzylisoquinoline alkaloid from natural products, has shown great potential in this area. Yet, systematic comparative studies on different tetrandrine modification sites (such as C-7 and C-14) are lacking, which has hindered the simultaneous optimization of its antitumor activity and synthetic feasibility. In this study, we focused on a C-7 modification strategy and designed and synthesized 38 novel tetrandrine sulfonate derivatives (including 31 new compounds) through an efficient one-step reaction. The in vitro antiproliferative activities of these derivatives were evaluated against four HCC cell lines (HepG-2, SMMC-7721, SK-Hep-1, and QGY-7701), and a systematic comparison with previously reported C-14 sulfonate derivatives was conducted. The results showed that all the C-7 derivatives exhibited good antiproliferative activities against HCC. Notably, compound 15 demonstrated significant antiproliferative activity against all tested cell lines, with IC

Indexed as

Antineoplastic AgentsBenzylisoquinolinesCarcinoma, HepatocellularLiver NeoplasmsApoptosisCell Line, TumorCell ProliferationHumansAntineoplastic AgentsBenzylisoquinolinestetrandrineCandidate drugCaspase-3-dependent apoptotic pathwayHCC cellsSulfonate derivativesTetrandrine

Identifiers

PMID41023382
PMCPMC12480866

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.