Evidence map›Paper›PMID 36324493›Full record

ReviewRSC medicinal chemistry2022

Current leishmaniasis drug discovery.

Alessandra Campbell Pinheiro, Marcus Vinícius Nora de Souza

Open access · greenAbstract readReview
In one paragraph

Review in RSC medicinal chemistry, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
9.4field-weighted citation impact, top 1% 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

26 citing papers in PubMed, 53 citations in OpenAlex.

  1. Article
  2. Article
  3. Silver-Pharmaceuticals (Basel, Switzerland) · 2026
    Article
  4. Review
  5. Review
  6. Article
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  17. Phytochemical profiling andFrontiers in chemistry · 2024
    Article
  18. Rational repurposing, synthesis,Journal of enzyme inhibition and medicinal chemistry · 2023
    Article
  19. Article
  20. Synthesis and Biophysical and Biological Studies ofJournal of medicinal chemistry · 2023
    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

2 authors at 1 institution in 1 country.

Alessandra Campbell PinheiroInstituto de Tecnologia em Fármacos - Farmanguinhos/FIOCRUZ Rio de Janeiro RJ Brazil alessandra.pinheiro@far.fiocruz.br marcus.nora@far.fiocruz.br.ORCID https://orcid.org/0000-0002-0121-0937
Marcus Vinícius Nora de SouzaInstituto de Tecnologia em Fármacos - Farmanguinhos/FIOCRUZ Rio de Janeiro RJ Brazil alessandra.pinheiro@far.fiocruz.br marcus.nora@far.fiocruz.br.ORCID https://orcid.org/0000-0003-1566-8110
Fundação Oswaldo Cruz · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Leishmaniasis is a complex protozoan infectious disease and, associated with malnutrition, poor health services and unavailability of prophylactic control measures, neglected populations are particularly affected. Current drug regimens are outdated and associated with some drawbacks, such as cytotoxicity and resistance, and the development of novel, efficacious and less toxic drug regimens is urgently required. In addition, leishmanial pathogenesis is not well established or understood, and a prophylactic vaccine is an unfulfilled goal. Human kinetoplastid protozoan infections, including leishmaniasis, have been neglected for many years, and in an attempt to overcome this situation, some new drug targets were recently identified, enabling the development of new drugs and vaccines. Compounds from new drug classes have also shown excellent antileishmanial activities, some of the most promising ones included in clinical trials, and could be a hope to control the disease burden of this endemic disease in the near future. In this review, we discuss the limitations of current control methods, explore the wide range of compounds that are being screened and identified as antileishmanial drug prototypes, summarize the advances in identifying new drug targets aiming at innovative treatments and explore the state-of-art vaccine development field, including immunomodulation strategies.

Identifiers

PMID36324493
PMCPMC9491386
OpenAlexW4293124251

What OpenQuestion holds

Textmetadata
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.