Evidence map›Paper›PMID 29223887›Full record

ArticleEuropean journal of medicinal chemistry2018

A minimalistic approach to develop new anti-apicomplexa polyamines analogs.

Esteban A Panozzo-Zénere, Exequiel O J Porta, Gustavo Arrizabalaga, Lucía Fargnoli, Shabana I Khan, Babu L Tekwani, Guillermo R Labadie

Open access · greenAbstract read
In one paragraph

Article in European journal of medicinal chemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.4field-weighted citation impact, top 42% 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

4 citing papers in PubMed, 10 citations in OpenAlex.

  1. Mechanistic Exploration ofPharmaceuticals (Basel, Switzerland) · 2026
    Article
  2. Article
  3. Review
  4. Establishment ofPathogens (Basel, Switzerland) · 2021
    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

7 authors at 3 institutions in 2 countries.

Esteban A Panozzo-ZénereInstituto de Química Rosario (IQUIR-CONICET), Facultad de Ciencias Bioquímicas y Farmacéuticas, Universidad Nacional de Rosario, Suipacha 531, S2002LRK, Rosario, Argentina.
Exequiel O J PortaInstituto de Química Rosario (IQUIR-CONICET), Facultad de Ciencias Bioquímicas y Farmacéuticas, Universidad Nacional de Rosario, Suipacha 531, S2002LRK, Rosario, Argentina.
Gustavo ArrizabalagaDepartments of Microbiology and Immunology, Indiana University, School of Medicine, Indianapolis, IN 46202, USA.
Lucía FargnoliInstituto de Química Rosario (IQUIR-CONICET), Facultad de Ciencias Bioquímicas y Farmacéuticas, Universidad Nacional de Rosario, Suipacha 531, S2002LRK, Rosario, Argentina.
Shabana I KhanNational Center for Natural Products Research & Department of Biomolecular Sciences, School of Pharmacy, University of Mississippi, MS 38677, USA.
Babu L TekwaniNational Center for Natural Products Research & Department of Biomolecular Sciences, School of Pharmacy, University of Mississippi, MS 38677, USA.
Guillermo R LabadieInstituto de Química Rosario (IQUIR-CONICET), Facultad de Ciencias Bioquímicas y Farmacéuticas, Universidad Nacional de Rosario, Suipacha 531, S2002LRK, Rosario, Argentina; Departamento de Química Orgánica, Facultad de Ciencias Bioquímicas y Farmacéuticas, Universidad Nacional de Rosario, Suipacha 531, S2002LRK, Rosario, Argentina. Electronic address: labadie@iquir-conicet.gov.ar.
Consejo Nacional de Investigaciones Científicas y Técnicas · ARUniversity of Mississippi · USIndiana University – Purdue University Indianapolis · US

Funding

Calcium signaling in the parasitophorous vacuole of Toxoplasma gondiiR21AI119516 · NIAID · INDIANA UNIVERSITY INDIANAPOLIS · PI ARRIZABALAGA, GUSTAVO A · 2015 to 2016
$460k
Dissecting the role of Toxoplasma CDPK3 in parasite propagation and virulenceR21AI108393 · NIAID · INDIANA UNIVERSITY INDIANAPOLIS · PI ARRIZABALAGA, GUSTAVO A · 2015 to 2016
$429k
NIAID NIH HHS R21 AI108393NIAID NIH HHS R21 AI119516
6 · The paper itself

Abstract

The development of new chemical entities against the major diseases caused by parasites is highly desired. A library of thirty diamines analogs following a minimalist approach and supported by chemoinformatics tools have been prepared and evaluated against apicomplexan parasites. Different member of the series of N,N'-disubstituted aliphatic diamines shown in vitro activities at submicromolar concentrations and high levels of selectivity against Toxoplasma gondii and in chloroquine-sensitive and resistant-strains of Plasmodium falciparum. In order to demonstrate the importance of the secondary amines, ten N,N,N',N'-tetrasubstituted aliphatic diamines derivatives were synthesized being considerably less active than their disubstituted counterpart. Theoretical studies were performed to establish the electronic factors that govern the activity of the compounds.

Indexed as

Antiparasitic AgentsApicomplexaDose-Response Relationship, DrugMolecular StructureParasitic Sensitivity TestsPlasmodium falciparumPolyaminesStructure-Activity RelationshipToxoplasmaAntiparasitic AgentsPolyaminesAnti-apicomplexaCheminformaticsN,N′-disubstituted diaminesNTDsPolyamines

Identifiers

PMID29223887
PMCPMC6209510
OpenAlexW2773244784

What OpenQuestion holds

Textmetadata
LicenceTDM
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.