Evidence map›Paper›PMID 32772176›Full record

ArticleParasitology research2020

Alsinol, an arylamino alcohol derivative active against Plasmodium, Babesia, Trypanosoma, and Leishmania: past and new outcomes.

Maria H Arias, Miguel Quiliano, Sandra Bourgeade-Delmas, Isabelle Fabing, Isabelle Chantal, David Berthier, Cécile Minet, Veronique Eparvier, Jonathan Sorres, Didier Stien and 5 more

Abstract read
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In one paragraph

Article in Parasitology research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Targeting theHeliyon · 2022
    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

15 authors.

Maria H AriasFacultad de Ciencias, Departamento de Farmacia, Grupo de Investigación FaMeTra (Farmacología de la Medicina Tradicional y Popular), Universidad Nacional de Colombia, Sede Bogotá, Carrera 30 45-03, Bogotá D.C., 111321, Colombia.ORCID https://orcid.org/0000-0002-1011-5157
Miguel QuilianoFaculty of Health Sciences, Centre for Research and Innovation, Universidad Peruana de Ciencias Aplicadas (UPC), 15023, Lima, Peru.ORCID https://orcid.org/0000-0002-6777-2529
Sandra Bourgeade-DelmasUMR 152 PHARMA-DEV, Institut de Recherche pour le Développement IRD, Université de Toulouse UPS, Toulouse, France.ORCID https://orcid.org/0000-0001-9027-765X
Isabelle FabingLaboratoire de Synthèse et Physicochimie de Molécules d'Intérêt Biologique (SPCMIB), Centre National de la Recherche Scientifique (CNRS), 31062, Cedex 09, Toulouse, France.
Isabelle ChantalUMR INTERTRYP, CIRAD, F-34398, Montpellier, France.ORCID https://orcid.org/0000-0002-3429-484X
David BerthierUMR INTERTRYP, CIRAD, F-34398, Montpellier, France.ORCID https://orcid.org/0000-0002-3283-6588
Cécile MinetUMR INTERTRYP, CIRAD, F-34398, Montpellier, France.ORCID https://orcid.org/0000-0002-9287-1481
Veronique EparvierICSN-CNRS UPR 2301 Équipe "Métabolites de végétaux et micro-organismes associés: isolement, synthèse et bioactivité", 91198 cedex, Gif-sur-Yvette, France.ORCID https://orcid.org/0000-0002-2954-0866
Jonathan SorresICSN-CNRS UPR 2301 Équipe "Métabolites de végétaux et micro-organismes associés: isolement, synthèse et bioactivité", 91198 cedex, Gif-sur-Yvette, France.
Didier StienLaboratoire de Biodiversité et Biotechnologie Microbienne, LBBM, Observatoire Océanologique, CNRS, Sorbonne Université, 66650, Banyuls-sur-mer, France.ORCID https://orcid.org/0000-0002-9950-5361
Silvia GalianoFacultad de Farmacia y Nutrición, Departamento de Química Orgánica y Farmacéutica, Universidad de Navarra, Campus Universitario, 31008, Pamplona, Spain.
Ignacio AldanaFacultad de Farmacia y Nutrición, Departamento de Química Orgánica y Farmacéutica, Universidad de Navarra, Campus Universitario, 31008, Pamplona, Spain.
Alexis ValentinUMR 152 PHARMA-DEV, Institut de Recherche pour le Développement IRD, Université de Toulouse UPS, Toulouse, France.ORCID https://orcid.org/0000-0002-2133-112X
Giovanny GaravitoFacultad de Ciencias, Departamento de Farmacia, Grupo de Investigación FaMeTra (Farmacología de la Medicina Tradicional y Popular), Universidad Nacional de Colombia, Sede Bogotá, Carrera 30 45-03, Bogotá D.C., 111321, Colombia. ggaravitoc@unal.edu.co.ORCID https://orcid.org/0000-0002-6055-0501
Eric DeharoUMR 152 PHARMA-DEV, Institut de Recherche pour le Développement IRD, Université de Toulouse UPS, Toulouse, France.ORCID https://orcid.org/0000-0002-5664-9517

Funding

Departamento Administrativo de Ciencia, Tecnología e Innovación Convocatoria 647, Doctorados Nacionales 2014Departamento Administrativo de Ciencia, Tecnología e Innovación ECOSNORD 2013Institut de Recherche pour le Développement IRD Maturation projects programmeLaboratoire d'Excellence (Labex) Parafrap N8ANR-11-LABX-0024Ministère des Affaires Étrangères ECOSNORD 2013PIUNA Project-University of Navarra and Foundation CAN 70391Programa Nacional de Innovación para la competitividad y productividad" (Innóvate-Perú) 065-FINCYT-BDE-2014Universidad Nacional de Colombia Vicedecanatura de Investigación, Facultad de Ciencias
6 · The paper itself

Abstract

Malaria, babesiosis, trypanosomosis, and leishmaniasis are some of the most life-threatening parasites, but the range of drugs to treat them is limited. An effective, safe, and low-cost drug with a large activity spectrum is urgently needed. For this purpose, an aryl amino alcohol derivative called Alsinol was resynthesized, screened in silico, and tested against Plasmodium, Babesia, Trypanosoma, and Leishmania. In silico Alsinol follows the Lipinski and Ghose rules. In vitro it had schizontocidal activity against Plasmodium falciparum and was able to inhibit gametocytogenesis; it was particularly active against late gametocytes. In malaria-infected mice, it showed a dose-dependent activity similar to chloroquine. It demonstrated a similar level of activity to reference compounds against Babesia divergens, and against promastigotes, and amastigotes stages of Leishmania in vitro. It inhibited the in vitro growth of two African animal strains of Trypanosoma but was ineffective in vivo in our experimental conditions. It showed moderate toxicity in J774A1 and Vero cell models. The study demonstrated that Alsinol has a large spectrum of activity and is potentially affordable to produce. Nevertheless, challenges remain in the process of scaling up synthesis, creating a suitable clinical formulation, and determining the safety margin in preclinical models.

Indexed as

Amino AlcoholsAnimalsAntiprotozoal AgentsBabesiaCell SurvivalChlorocebus aethiopsDisease Models, AnimalLeishmaniaLife Cycle StagesMicePlasmodiumProtozoan InfectionsTreatment OutcomeTrypanosomaVero CellsAmino AlcoholsAntiprotozoal AgentsAlsinolAntiprotozoanBabesiaLeishmaniaPlasmodium falciparum gametocytesTrypanosoma

Identifiers

What OpenQuestion holds

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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.