Evidence map›Paper›PMID 34894961›Full record

ArticleJournal of enzyme inhibition and medicinal chemistry2022

Synthesis and biological evaluation of celastrol derivatives as potent antitumor agents with STAT3 inhibition.

Shaohua Xu, Ruolan Fan, Lu Wang, Weishen He, Haixia Ge, Hailan Chen, Wen Xu, Jian Zhang, Wei Xu, Yaqian Feng and 1 more

Open access · goldAbstract read
In one paragraph

Article in Journal of enzyme inhibition and medicinal chemistry, 2022. 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
1.9field-weighted citation impact, top 13% of its field
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, 13 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Frontiers in immunology · 2023
    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

11 authors at 6 institutions in 2 countries.

Shaohua XuCollege of Pharmacy, Fujian University of Traditional Chinese Medicine, Fuzhou, P.R. China.ORCID 0000-0003-2967-6824
Ruolan FanCollege of Pharmacy, Fujian University of Traditional Chinese Medicine, Fuzhou, P.R. China.
Lu WangNational Center of Colorectal Disease, Nanjing Hospital of Chinese Medicine Affiliated to Nanjing University of Chinese Medicine, Nanjing, P.R. China.
Weishen HeBiology Department, Boston College, Brighton, MA, USA.
Haixia GeSchool of Life Sciences, Huzhou University, Huzhou, P.R. China.
Hailan ChenCollege of Pharmacy, Fujian University of Traditional Chinese Medicine, Fuzhou, P.R. China.
Wen XuCollege of Pharmacy, Fujian University of Traditional Chinese Medicine, Fuzhou, P.R. China.
Jian ZhangState Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing, P.R. China.
Wei XuCollege of Pharmacy, Fujian University of Traditional Chinese Medicine, Fuzhou, P.R. China.
Yaqian FengSchool of Pharmaceutical Sciences, Key Laboratory of Bioorganic Phosphorus Chemistry and Chemical Biology (Ministry of Education), Tsinghua University, Beijing, P.R. China.
Zhimin FanNational Center of Colorectal Disease, Nanjing Hospital of Chinese Medicine Affiliated to Nanjing University of Chinese Medicine, Nanjing, P.R. China.
Fujian University of Traditional Chinese Medicine · CNNanjing University of Chinese Medicine · CNBoston College · USChina Pharmaceutical University · CNHuzhou University · CNTsinghua University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Using STAT3 inhibitors as a potential strategy in cancer therapy have attracted much attention. Recently, celastrol has been reported that it could directly bind to and suppress the activity of STAT3 in the cardiac dysfunction model. To explore more effective STAT3 inhibiting anti-tumour drug candidates, we synthesised a series of celastrol derivatives and biologically evaluated them with several human cancer cell lines. The western blotting analysis showed that compound

Indexed as

Antineoplastic AgentsApoptosisCell CycleCell ProliferationDose-Response Relationship, DrugDrug Screening Assays, AntitumorHumansModels, MolecularMolecular StructurePentacyclic TriterpenesSTAT3 Transcription FactorStructure-Activity RelationshipTumor Cells, CulturedAntineoplastic AgentscelastrolPentacyclic TriterpenesSTAT3 protein, humanSTAT3 Transcription Factoranti-tumourCelastrolcolorectal cancer organoidSTAT3 inhibitorstructural modification

Identifiers

PMID34894961
PMCPMC8667935
OpenAlexW4200126024

What OpenQuestion holds

Textmetadata
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.