Evidence map›Paper›PMID 31052607›Full record

ArticleMolecules (Basel, Switzerland)2019

Pyrimidine 2,4-Diones in the Design of New HIV RT Inhibitors.

Roberto Romeo, Daniela Iannazzo, Lucia Veltri, Bartolo Gabriele, Beatrice Macchi, Caterina Frezza, Francesca Marino-Merlo, Salvatore V Giofrè

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

10 citing papers in PubMed, 48 citations in OpenAlex.

  1. Article
  2. Article
  3. Bioinspired Pyrano[2,3-Biomimetics (Basel, Switzerland) · 2024
    Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. 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

8 authors at 4 institutions in 1 country.

Roberto RomeoDipartimento di Scienze chimiche, biologiche, farmaceutiche ed ambientali, Università di Messina, Via S.S. Annunziata, 98168 Messina, Italy. robromeo@unime.it.
Daniela IannazzoDipartimento di Ingegneria, Università di Messina, Contrada Di Dio, 98166 Messina, Italy. diannazzo@unime.it.
Lucia VeltriDipartimento di Chimica e tecnologie chimiche, Università della Calabria,Via P. Bucci 12/C, 87036 Arcavacata di Rende, Italy. lucia.veltri@unical.it.
Bartolo GabrieleDipartimento di Chimica e tecnologie chimiche, Università della Calabria,Via P. Bucci 12/C, 87036 Arcavacata di Rende, Italy. bartolo.gabriele@unical.it.
Beatrice MacchiDipartimento di Scienze e Tecnologie Chimiche, Università di Roma "Tor Vergata", 00133 Roma, Italy. macchi@med.uniroma2.it.
Caterina FrezzaDipartimento di Scienze e Tecnologie Chimiche, Università di Roma "Tor Vergata", 00133 Roma, Italy. catafrezza@hotmail.it.
Francesca Marino-MerloIRCCS Centro Neurolesi "Bonino-Pulejo", Messina, Italy. fmarino@unime.it.
Salvatore V GiofrèDipartimento di Scienze chimiche, biologiche, farmaceutiche ed ambientali, Università di Messina, Via S.S. Annunziata, 98168 Messina, Italy. sgiofre@unime.it.
University of Messina · ITUniversity of Calabria · ITUniversity of Rome Tor Vergata · ITCentro Neurolesi Bonino Pulejo · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The pyrimidine nucleus is a versatile core in the development of antiretroviral agents. On this basis, a series of pyrimidine-2,4-diones linked to an isoxazolidine nucleus have been synthesized and tested as nucleoside analogs, endowed with potential anti-HIV (human immunodeficiency virus) activity. Compounds

Indexed as

Drug DesignChemistry Techniques, SyntheticHIV-1HumansModels, MolecularMolecular StructureProtein BindingPyrimidinesQuantitative Structure-Activity RelationshipReverse Transcriptase InhibitorsPyrimidinesReverse Transcriptase Inhibitorsbiological activityHIV RT inhibitorsmolecular docking.Pyrimidine-2,4-dione derivativesreverse nucleosides

Identifiers

PMID31052607
PMCPMC6539630
OpenAlexW2942626681

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.