Evidence map›Paper›PMID 36176072›Full record

ArticleJournal of enzyme inhibition and medicinal chemistry2022

Design, synthesis and antitumor activity of 5-trifluoromethylpyrimidine derivatives as EGFR inhibitors.

Yaqing Zuo, Rongrong Li, Yan Zhang, Guochen Bao, Yi Le, Longjia Yan

Abstract 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 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Fourth-generation EGFR-TKI to overcome C797S mutation: past, present, and future.Journal of enzyme inhibition and medicinal chemistry · 2025
    Review
  2. Article
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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

6 authors.

Yaqing ZuoSchool of Pharmaceutical Sciences, Guizhou University, Guiyang, China.
Rongrong LiSchool of Pharmaceutical Sciences, Guizhou University, Guiyang, China.
Yan ZhangSchool of Pharmaceutical Sciences, Guizhou University, Guiyang, China.
Guochen BaoInstitute for Biomedical Materials and Devices (IBMD), Faculty of Science, University of Technology Sydney, Sydney, Australia.ORCID 0000-0001-5103-5009
Yi LeSchool of Pharmaceutical Sciences, Guizhou University, Guiyang, China.
Longjia YanSchool of Pharmaceutical Sciences, Guizhou University, Guiyang, China.ORCID 0000-0003-3703-6704

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A new series of 5-trifluoromethylpyrimidine derivatives were designed and synthesised as EGFR inhibitors. Three tumour cells A549, MCF-7, PC-3 and EGFR kinase were employed to evaluate their biological activities. The results were shown that most of the target compounds existed excellent antitumor activities. In particular, the IC

Indexed as

Antineoplastic AgentsProtein Kinase InhibitorsApoptosisCell ProliferationDose-Response Relationship, DrugDrug DesignDrug Screening Assays, AntitumorErbB ReceptorsMolecular StructureStructure-Activity RelationshipAntineoplastic AgentsErbB ReceptorsProtein Kinase InhibitorsantitumorEGFRinhibitorpyrimidinereagent

Identifiers

PMID36176072
PMCPMC9542405

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.