Evidence map›Paper›PMID 30782984›Full record

ArticleAntimicrobial agents and chemotherapy2019

Synthesis and Leishmanicidal Activity of Novel Urea, Thiourea, and Selenourea Derivatives of Diselenides.

Marta Díaz, Héctor de Lucio, Esther Moreno, Socorro Espuelas, Carlos Aydillo, Antonio Jiménez-Ruiz, Miguel Ángel Toro, Killian Jesús Gutiérrez, Victor Martínez-Merino, Alfonso Cornejo and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
5.5field-weighted citation impact, top 4% 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

12 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. NovelAntioxidants (Basel, Switzerland) · 2021
    Article
  9. Novel Selenoureas Based onMaterials (Basel, Switzerland) · 2021
    Article
  10. Article
  11. Article
  12. 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

13 authors at 3 institutions in 1 country.

Marta DíazUniversidad de Navarra, Facultad de Farmacia y Nutrición, Departamento de Tecnología y Química Farmacéuticas, Pamplona, Spain.
Héctor de LucioDepartamento de Biología de Sistemas, Universidad de Alcalá, Madrid, Spain.
Esther MorenoUniversidad de Navarra, Facultad de Farmacia y Nutrición, Departamento de Tecnología y Química Farmacéuticas, Pamplona, Spain.
Socorro EspuelasUniversidad de Navarra, Facultad de Farmacia y Nutrición, Departamento de Tecnología y Química Farmacéuticas, Pamplona, Spain.
Carlos AydilloUniversidad de Navarra, Facultad de Farmacia y Nutrición, Departamento de Tecnología y Química Farmacéuticas, Pamplona, Spain.
Antonio Jiménez-RuizDepartamento de Biología de Sistemas, Universidad de Alcalá, Madrid, Spain.
Miguel Ángel ToroDepartamento de Biología de Sistemas, Universidad de Alcalá, Madrid, Spain.
Killian Jesús GutiérrezDepartamento de Biología de Sistemas, Universidad de Alcalá, Madrid, Spain.
Victor Martínez-MerinoDepartamento de Química Aplicada, Universidad Pública de Navarra, Pamplona, Spain.
Alfonso CornejoDepartamento de Química Aplicada, Universidad Pública de Navarra, Pamplona, Spain.
Juan Antonio PalopUniversidad de Navarra, Facultad de Farmacia y Nutrición, Departamento de Tecnología y Química Farmacéuticas, Pamplona, Spain.
Carmen SanmartínUniversidad de Navarra, Facultad de Farmacia y Nutrición, Departamento de Tecnología y Química Farmacéuticas, Pamplona, Spain sanmartin@unav.es.ORCID 0000-0003-3431-7826
Daniel PlanoUniversidad de Navarra, Facultad de Farmacia y Nutrición, Departamento de Tecnología y Química Farmacéuticas, Pamplona, Spain.
Instituto de Salud Pública de Navarra · ESUniversidad de Alcalá · ESUniversidad Publica de Navarra · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A novel series of thirty-one N-substituted urea, thiourea, and selenourea derivatives containing diphenyldiselenide entities were synthesized, fully characterized by spectroscopic and analytical methods, and screened for their

Indexed as

Antiprotozoal AgentsHumansLeishmania infantumMacrophagesNADH, NADPH OxidoreductasesOrganoselenium CompoundsParasitic Sensitivity TestsStructure-Activity RelationshipThioureaUreaAntiprotozoal AgentsNADH, NADPH OxidoreductasesOrganoselenium CompoundsselenoureaThioureatrypanothione reductaseUreaseleniumselenoureathioureatrypanothione reductaseurea

Identifiers

PMID30782984
PMCPMC6496061
OpenAlexW2916494161

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.