Evidence map›Paper›PMID 34778907›Full record

ArticleParasitology research2022

Synthesis and in silico ADME/Tox profiling studies of heterocyclic hybrids based on chloroquine scaffolds with potential antimalarial activity.

Hegira Ramírez, Esteban Fernandez-Moreira, Juan R Rodrigues, Michael R Mijares, Jorge E Ángel, Jaime E Charris

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Article in Parasitology research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

6 authors.

Hegira RamírezOrganic Synthesis Laboratory, Faculty of Pharmacy, Central University of Venezuela, Caracas, 472061041-A, Los Chaguaramos, Venezuela. hegira.ramirez@udla.edu.ec.ORCID http://orcid.org/0000-0003-1916-6118
Esteban Fernandez-MoreiraEscuela de Medicina, Universidad Espíritu Santo, Samborondón, Ecuador.
Juan R RodriguesDepartamento de Tecnología de Procesos Biológicos y Bioquímicos, División de Ciencias Biológicas, Universidad Simón Bolívar, Valle de Sartenejas, Caracas, 9063971, Venezuela.
Michael R MijaresBiotechnology Unit, Faculty of Pharmacy, Central University of Venezuela, Caracas, 472061041-A, Los Chaguaramos, Venezuela.
Jorge E ÁngelOrganic Synthesis Laboratory, Design and Pharmacological Evaluation of New Products, Experimental Faculty of Science, Central University of Venezuela, Zulia University, Maracaibo, Venezuela.
Jaime E CharrisOrganic Synthesis Laboratory, Faculty of Pharmacy, Central University of Venezuela, Caracas, 472061041-A, Los Chaguaramos, Venezuela. jaime.charris@ucv.ve.ORCID http://orcid.org/0000-0003-4404-2619

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A series of heterocyclic chloroquine hybrids containing either a β-phenethylamine fragment or a 2-aminoindane moiety were synthesized and screened in vitro as inhibitors of β-hematin formation and in vivo for their antimalarial activity against chloroquine-sensitive strains of Plasmodium berghei ANKA. Although these new compounds were not found to be more active than chloroquine in vivo, all new compounds significantly reduced heme crystallization with IC

Indexed as

AntimalarialsMalariaChloroquineHumansPlasmodium bergheiPlasmodium falciparumAntimalarialsChloroquine2-AminoindaneChloroquineHemozoinMalariaβ-Phenethylamine

Identifiers

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Registered trials

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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.