Evidence map›Paper›PMID 28446339›Full record

ArticleChimia2017

Progress in the Optimization of 4(1

Fabian Brockmeyer, Roman Manetsch

Abstract read
In one paragraph

Article in Chimia, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

2 authors.

Fabian BrockmeyerNortheastern University Department of Chemistry and Chemical Biology and Department of Pharmaceutical Sciences 360 Huntington Avenue, HT102, Boston, Massachusetts 02115, USA.
Roman ManetschNortheastern University Department of Chemistry and Chemical Biology and Department of Pharmaceutical Sciences 360 Huntington Avenue, HT102, Boston, Massachusetts 02115, USA;, Email: r.manetsch@northeastern.edu.

Funding

Drugs targeting erythrocytic and exoerythrocytic stages of malariaR01GM097118 · NIGMS · UNIVERSITY OF SOUTH FLORIDA · PI MANETSCH, ROMAN · 2011 to 2015
$1.3M
NIGMS NIH HHS R01 GM097118
6 · The paper itself

Abstract

Malaria is one of the leading infectious diseases occurring mainly in tropical and subtropical areas. Although available antimalarial tools have reduced the number of fatalities, there is still an urgent need for the development of new and more efficacious treatments to cure and eradicate malaria especially due to emerging resistance to all antimalarial drugs. Research was initiated to revisit antimalarial compounds which were deemed unsuitable as a result of poor understanding of physicochemical properties and the optimization thereof. The 4(1H)-quinolones are a class of compounds with demonstrated activity against malaria parasites. Recent optimization of the long-known core led to two highly promising compounds, i.e. P4Q-391 and ELQ-300, with great selective activity against all stages of the parasite's life cycle and good physicochemical properties. In this paper, we discuss the key steps on the way to these compounds, which fuel hope to find a suitable treatment for the prevention, cure and eradication of malaria.

Indexed as

AnimalsAntimalarialsMicePlasmodium falciparumQuinolonesStructure-Activity Relationship6-Chloro-7-methoxy-2-methyl-3-(4-(4-(trifluoromethoxy)phenoxy)phenyl)quinolin-4(1H)-oneAntimalarialsQuinolones

Identifiers

PMID28446339
PMCPMC9257372

What OpenQuestion holds

Textmetadata
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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.