Evidence map›Paper›PMID 28203273›Full record

ArticleChemistry Central journal2017

Synthesis and biological evaluation of the new 1,3-dimethylxanthine derivatives with thiazolidine-4-one scaffold.

Sandra Constantin, Florentina Geanina Lupascu, Maria Apotrosoaei, Ioana Mirela Vasincu, Dan Lupascu, Frederic Buron, Sylvain Routier, Lenuta Profire

Open access · goldAbstract read
In one paragraph

Article in Chemistry Central journal, 2017. 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
1.4field-weighted citation impact, top 22% 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

3 citing papers in PubMed, 28 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
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

8 authors at 2 institutions in 2 countries.

Sandra ConstantinThe Department of Pharmaceutical Chemistry, The Faculty of Pharmacy, "Grigore T. Popa" University of Medicine and Pharmacy, No. 16 University Street, Iasi, 700115 Romania.
Florentina Geanina LupascuThe Department of Pharmaceutical Chemistry, The Faculty of Pharmacy, "Grigore T. Popa" University of Medicine and Pharmacy, No. 16 University Street, Iasi, 700115 Romania.
Maria ApotrosoaeiThe Department of Pharmaceutical Chemistry, The Faculty of Pharmacy, "Grigore T. Popa" University of Medicine and Pharmacy, No. 16 University Street, Iasi, 700115 Romania.
Ioana Mirela VasincuThe Department of Pharmaceutical Chemistry, The Faculty of Pharmacy, "Grigore T. Popa" University of Medicine and Pharmacy, No. 16 University Street, Iasi, 700115 Romania.
Dan LupascuThe Department of Pharmaceutical Chemistry, The Faculty of Pharmacy, "Grigore T. Popa" University of Medicine and Pharmacy, No. 16 University Street, Iasi, 700115 Romania.
Frederic BuronInstitut de Chimie Organique et Analytique, ICOA, Univ Orleans, Orleans, France.
Sylvain RoutierInstitut de Chimie Organique et Analytique, ICOA, Univ Orleans, Orleans, France.
Lenuta ProfireThe Department of Pharmaceutical Chemistry, The Faculty of Pharmacy, "Grigore T. Popa" University of Medicine and Pharmacy, No. 16 University Street, Iasi, 700115 Romania.
Grigore T. Popa University of Medicine and Pharmacy · ROInstitut de Chimie Organique et Analytique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe xanthine structure has proved to be an important scaffold in the process of developing a wide variety of biologically active molecules such as bronchodilator, hypoglycemiant, anticancer and anti-inflammatory agents. It is known that hyperglycemia generates reactive oxygen species which are involved in the progression of diabetes mellitus and its complications. Therefore, the development of new compounds with antioxidant activity could be an important therapeutic strategy against this metabolic syndrome.

resultsNew thiazolidine-4-one derivatives with xanthine structure have been synthetized as potential antidiabetic drugs. The structure of the synthesized compounds was confirmed by using spectral methods (FT-IR,

conclusionsFor several thiazolidine-4-one derivatives the antioxidant effect of was superior to that of their corresponding hydrazone derivatives. The most active compound was

Indexed as

1,3-Dimethylxanthine1,3-Thiazolidine-4-oneAntioxidant effectsSpectral methods

Identifiers

PMID28203273
PMCPMC5289128
OpenAlexW2583609851

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.