Evidence map›Paper›PMID 35947400›Full record

ReviewChirality2022

A recent update on new synthetic chiral compounds with antileishmanial activity.

Michele Verboni, Diego Olivieri, Simone Lucarini

Abstract readReview
In one paragraph

Review in Chirality, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. 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

3 authors.

Michele VerboniDepartment of Biomolecular Science, University of Urbino Carlo Bo, Urbino, Italy.ORCID 0000-0001-5648-521X
Diego OlivieriDepartment of Biomolecular Science, University of Urbino Carlo Bo, Urbino, Italy.ORCID 0000-0001-9411-4487
Simone LucariniDepartment of Biomolecular Science, University of Urbino Carlo Bo, Urbino, Italy.ORCID 0000-0002-3667-1207

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Parasitic diseases, including malaria, leishmaniasis, and trypanosomiasis, affect billions of people and are responsible for almost 500,000 deaths/year. In particular, leishmaniasis, a neglected tropical disease, is considered a global public health problem because current drugs have several drawbacks including to toxicity, high cost, and drug resistance, which result in a lack of effective and readily available therapies. Therefore, the synthesis of new, safe, and effective molecules still requires the attention of the scientific community. Moreover, it is well known that chirality plays a crucial role in the antiparasitic activity of molecules, driving the design of their synthesis. Therefore, in this review we report a recent update on new chiral compounds with promising antileishmanial activity, focusing on synthetic approaches. Where reported, in most cases the enantiopure compound has shown better potency against the protozoa than its enantiomer or corresponding racemic mixture.

Indexed as

Antiprotozoal AgentsLeishmaniasisHumansStereoisomerismAntiprotozoal Agentschiral catalysischiral poolchiral resolutionimidazoxazinesimidazoxazoleskinetic resolutionleishmaniamedicinal chemistrynatural productspeptides

Identifiers

PMID35947400
PMCPMC9543214

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.