Evidence map›Paper›PMID 30103421›Full record

ArticleMolecules (Basel, Switzerland)2018

Synthesis of 2,6-Diamino-Substituted Purine Derivatives and Evaluation of Cell Cycle Arrest in Breast and Colorectal Cancer Cells.

Bartolomeo Bosco, Andrea Defant, Andrea Messina, Tania Incitti, Denise Sighel, Angela Bozza, Yari Ciribilli, Alberto Inga, Simona Casarosa, Ines Mancini

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.6field-weighted citation impact, top 35% 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

6 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Synthesis and Cytotoxic Activity of the Derivatives ofMolecules (Basel, Switzerland) · 2023
    Article
  4. Article
  5. Heterocycles in Medicinal Chemistry.Molecules (Basel, Switzerland) · 2019
    Article
  6. 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.

Bartolomeo BoscoCentre for Integrative Biology (CIBIO), University of Trento, Via Sommarive 9, 38123 Trento, Italy. bartolomeo.bosco@unitn.it.
Andrea DefantLaboratory of Bioorganic Chemistry, Department of Physics, University of Trento, Via Sommarive 14, 38123 Trento, Italy. andrea.defant@yahoo.it.
Andrea MessinaCentre for Integrative Biology (CIBIO), University of Trento, Via Sommarive 9, 38123 Trento, Italy. andrea.messina@unitn.it.
Tania IncittiCentre for Integrative Biology (CIBIO), University of Trento, Via Sommarive 9, 38123 Trento, Italy. tania.incitti@gmail.com.ORCID 0000-0002-5573-1914
Denise SighelCentre for Integrative Biology (CIBIO), University of Trento, Via Sommarive 9, 38123 Trento, Italy. denise.sighel@unitn.it.
Angela BozzaCentre for Integrative Biology (CIBIO), University of Trento, Via Sommarive 9, 38123 Trento, Italy. angela.bozza@aulss8.veneto.it.
Yari CiribilliCentre for Integrative Biology (CIBIO), University of Trento, Via Sommarive 9, 38123 Trento, Italy. yari.ciribilli@unitn.it.
Alberto IngaCentre for Integrative Biology (CIBIO), University of Trento, Via Sommarive 9, 38123 Trento, Italy. alberto.inga@unitn.it.ORCID 0000-0002-8767-1637
Simona CasarosaCentre for Integrative Biology (CIBIO), University of Trento, Via Sommarive 9, 38123 Trento, Italy. simona.casarosa@unitn.it.
Ines ManciniLaboratory of Bioorganic Chemistry, Department of Physics, University of Trento, Via Sommarive 14, 38123 Trento, Italy. ines.mancini@unitn.it.
University of Trento · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Reversine is a potent antitumor 2,6-diamino-substituted purine acting as an Aurora kinases inhibitor and interfering with cancer cell cycle progression. In this study we describe three reversine-related molecules, designed by docking calculation, that present structural modifications in the diamino units at positions 2 and 6. We investigated the conformations of the most stable prototropic tautomers of one of these molecules, the

Indexed as

Antineoplastic AgentsBreast NeoplasmsCell Cycle CheckpointsCell Line, TumorCell SurvivalChemistry Techniques, SyntheticColorectal NeoplasmsFemaleHumansMaleMicrowavesMolecular StructurePurinesStructure-Activity RelationshipAntineoplastic AgentsPurinescell cycle arrestendoreduplicationmicrowave-assisted synthesismolecular dockingp53reversine

Identifiers

PMID30103421
PMCPMC6222518
OpenAlexW2887009936

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.