Evidence map›Paper›PMID 30108826›Full record

ArticleMedChemComm2017

Design, synthesis and pharmacological evaluation of new 2-oxo-quinoline derivatives containing α-aminophosphonates as potential antitumor agents.

Yan-Cheng Yu, Wen-Bin Kuang, Ri-Zhen Huang, Yi-Lin Fang, Ye Zhang, Zhen-Feng Chen, Xian-Li Ma

Open access · bronzeAbstract read
In one paragraph

Article in MedChemComm, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.1field-weighted citation impact, top 26% 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

8 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. 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 at 2 institutions in 1 country.

Yan-Cheng YuCollege of Pharmacy , Guilin Medical University , Guilin 541004 , PR China . Email: zhangye81@126.com ; Email: mxl78@glmc.edu.cn ; ; Tel: +86 773 5895132.
Wen-Bin KuangState Key Laboratory for the Chemistry and Molecular Engineering of Medicinal Resources (Ministry of Education of China) , School of Chemistry and Pharmaceutical Sciences of Guangxi Normal University , Guilin 541004 , PR China . Email: chenzf@gxnu.edu.cn.
Ri-Zhen HuangState Key Laboratory for the Chemistry and Molecular Engineering of Medicinal Resources (Ministry of Education of China) , School of Chemistry and Pharmaceutical Sciences of Guangxi Normal University , Guilin 541004 , PR China . Email: chenzf@gxnu.edu.cn.
Yi-Lin FangState Key Laboratory for the Chemistry and Molecular Engineering of Medicinal Resources (Ministry of Education of China) , School of Chemistry and Pharmaceutical Sciences of Guangxi Normal University , Guilin 541004 , PR China . Email: chenzf@gxnu.edu.cn.
Ye ZhangCollege of Pharmacy , Guilin Medical University , Guilin 541004 , PR China . Email: zhangye81@126.com ; Email: mxl78@glmc.edu.cn ; ; Tel: +86 773 5895132.ORCID 0000-0002-6903-5602
Zhen-Feng ChenState Key Laboratory for the Chemistry and Molecular Engineering of Medicinal Resources (Ministry of Education of China) , School of Chemistry and Pharmaceutical Sciences of Guangxi Normal University , Guilin 541004 , PR China . Email: chenzf@gxnu.edu.cn.
Xian-Li MaCollege of Pharmacy , Guilin Medical University , Guilin 541004 , PR China . Email: zhangye81@126.com ; Email: mxl78@glmc.edu.cn ; ; Tel: +86 773 5895132.
Ministry of Education of the People's Republic of China · CNGuilin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A series of novel 2-oxo-quinoline derivatives containing α-aminophosphonates were designed and synthesized as antitumor agents. MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) assay results demonstrated that some compounds exhibited moderate to high inhibitory activity against HepG2, SK-OV-3 and NCI-H460 tumor cell lines, and most compounds showed much lower cytotoxicity against HL-7702 normal cells than 5-FU and cisplatin. The action mechanism of representative compound

Identifiers

PMID30108826
PMCPMC6072518
OpenAlexW2603120023

What OpenQuestion holds

Textmetadata
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.