Evidence map›Paper›PMID 24366088›Full record

ArticleMolecules (Basel, Switzerland)2013

1H-2,3-dihydroperimidine derivatives: a new class of potent protein tyrosine phosphatase 1B inhibitors.

Wen-Long Wang, Dong-Lin Yang, Li-Xin Gao, Chun-Lan Tang, Wei-Ping Ma, Hui-Hua Ye, Si-Qi Zhang, Ya-Nan Zhao, Hao-Jie Xu, Zhao Hu and 7 more

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

17 authors.

Wen-Long WangSchool of Pharmaceutical Science, Jiangnan University, Wuxi 214122, China. wwenlong2011@163.com.
Dong-Lin Yang
Li-Xin Gao
Chun-Lan Tang
Wei-Ping Ma
Hui-Hua Ye
Si-Qi Zhang
Ya-Nan Zhao
Hao-Jie Xu
Zhao Hu
Xia Chen
Wen-Hua Fan
Hai-Jun Chen
Jing-Ya Li
Fa-Jun Nan
Jia LiSchool of Pharmaceutical Science, Jiangnan University, Wuxi 214122, China. jli@mail.shcnc.ac.cn.
Bainian FengSchool of Pharmaceutical Science, Jiangnan University, Wuxi 214122, China. fanwenhua1987@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A series of 1H-2,3-dihydroperimidine derivatives was designed, synthesized, and evaluated as a new class of inhibitors of protein tyrosine phosphatase 1B (PTP1B) with IC50 values in the micromolar range. Compounds 46 and 49 showed submicromolar inhibitory activity against PTP1B, and good selectivity (3.48-fold and 2.10-fold respectively) over T-cell protein tyrosine phosphatases (TCPTP). These results have provided novel lead compounds for the design of inhibitors of PTP1B as well as other PTPs.

Indexed as

AnimalsCHO CellsCricetulusInhibitory Concentration 50KineticsMolecular StructureProtein Tyrosine Phosphatase, Non-Receptor Type 1QuinazolinesStructure-Activity RelationshipperimidineProtein Tyrosine Phosphatase, Non-Receptor Type 1Quinazolines

Identifiers

PMID24366088
PMCPMC6271978

What OpenQuestion holds

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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.