Evidence map›Paper›PMID 31867165›Full record

ArticleActa pharmaceutica Sinica. B2019

Discovery of WS-157 as a highly potent, selective and orally active EGFR inhibitor.

Pengxing He, Shenghui Niu, Shuai Wang, Xiaojing Shi, Siqi Feng, Linna Du, Xuyang Zhang, Zhilu Ma, Bin Yu, Hongmin Liu

Open access · diamondAbstract read
In one paragraph

Article in Acta pharmaceutica Sinica. B, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
2.6field-weighted citation impact, top 9% 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

4 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. 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

10 authors at 1 institution in 1 country.

Pengxing HeSchool of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou 450001, China.
Shenghui NiuSchool of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou 450001, China.
Shuai WangSchool of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou 450001, China.
Xiaojing ShiSchool of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou 450001, China.
Siqi FengSchool of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou 450001, China.
Linna DuSchool of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou 450001, China.
Xuyang ZhangSchool of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou 450001, China.
Zhilu MaSchool of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou 450001, China.
Bin YuSchool of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou 450001, China.
Hongmin LiuSchool of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou 450001, China.
Zhengzhou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

EGFR tyrosine kinase inhibitor (EGFR-TKI) has been used successfully in clinic for the treatment of solid tumors. In the present study, we reported the discovery of

Indexed as

Antitumor activityEGFR inhibitorTyrosine kinaseWS-157

Identifiers

PMID31867165
PMCPMC6900553
OpenAlexW2954417699

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.