Evidence map›Paper›PMID 23609622›Full record

ArticleMolecules (Basel, Switzerland)2013

New amide derivatives of quinoxaline 1,4-di-N-oxide with leishmanicidal and antiplasmodial activities.

Carlos Barea, Adriana Pabón, Silvia Pérez-Silanes, Silvia Galiano, German Gonzalez, Antonio Monge, Eric Deharo, Ignacio Aldana

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 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. In Vitro Evaluation of Esters of Quinoxaline-1,4-di-Pharmaceuticals (Basel, Switzerland) · 2025
    Article
  2. Article
  3. Review
  4. Quinoxaline Moiety: A Potential Scaffold againstMolecules (Basel, Switzerland) · 2021
    Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. 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.

Carlos BareaUnidad de Investigación y Desarrollo de Nuevos Medicamentos, Centro de Investigación en Farmacobiología Aplicada-CIFA, Universidad de Navarra, Pamplona 31080, Spain. cabareari@hotmail.com
Adriana Pabón
Silvia Pérez-Silanes
Silvia Galiano
German Gonzalez
Antonio Monge
Eric Deharo
Ignacio Aldana

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Malaria and leishmaniasis are two of the World's most important tropical parasitic diseases. Continuing with our efforts to identify new compounds active against malaria and leishmaniasis, twelve new 1,4-di-N-oxide quinoxaline derivatives were synthesized and evaluated for their in vitro antimalarial and antileishmanial activity against Plasmodium falciparum FCR-3 strain, Leishmania infantum and Leishmania amazonensis. Their toxicity against VERO cells (normal monkey kidney cells) was also assessed. The results obtained indicate that a cyclopentyl derivative had the best antiplasmodial activity (2.9 µM), while a cyclohexyl derivative (2.5 µM) showed the best activity against L. amazonensis, and a 3-chloropropyl derivative (0.7 µM) showed the best results against L. infantum. All these compounds also have a Cl substituent in the R⁷ position.

Indexed as

AmidesAnimalsAntimalarialsAntiparasitic AgentsChlorocebus aethiopsHumansInhibitory Concentration 50LeishmaniaLeishmania infantumOxidesParasitic Sensitivity TestsPlasmodiumPlasmodium falciparumQuinoxalinesStructure-Activity RelationshipVero CellsAmidesAntimalarialsAntiparasitic AgentsOxidesQuinoxalines

Identifiers

PMID23609622
PMCPMC6269706

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.