Evidence map›Paper›PMID 37340748›Full record

ReviewCurrent medicinal chemistry2024

Targeting Cysteine Proteases and their Inhibitors to Combat Trypanosomiasis.

Aloke Saha, Pushpa, Susmita Moitra, Deblina Basak, Sayandeep Brahma, Dipu Mondal, Sabir Hossen Molla, Asmita Samadder, Sisir Nandi

Abstract readReview
PubMed Publisher
In one paragraph

Review in Current medicinal chemistry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. IntegratedPharmaceuticals (Basel, Switzerland) · 2026
    Article
  3. 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

9 authors at 2 institutions in 1 country.

Aloke SahaCell and Developmental Biology Special, Department of Zoology, University of Kalyani, Kalyani, Nadia, 741235, India.ORCID 0000-0001-9985-3481
PushpaCell and Developmental Biology Special, Department of Zoology, University of Kalyani, Kalyani, Nadia, 741235, India.ORCID 0000-0002-7992-3582
Susmita MoitraCell and Developmental Biology Special, Department of Zoology, University of Kalyani, Kalyani, Nadia, 741235, India.ORCID 0000-0003-4138-9262
Deblina BasakEndocrinology Special, Department of Zoology, University of Kalyani, Kalyani, Nadia, 741235, India.ORCID 0000-0001-5695-0441
Sayandeep BrahmaCell and Developmental Biology Special, Department of Zoology, University of Kalyani, Kalyani, Nadia, 741235, India.ORCID 0000-0001-6357-3170
Dipu MondalCell and Developmental Biology Special, Department of Zoology, University of Kalyani, Kalyani, Nadia, 741235, India.ORCID 0000-0001-9722-6804
Sabir Hossen MollaParasitology Laboratory, Department of Zoology, University of Kalyani, Kalyani, Nadia, 741235, India.ORCID 0000-0003-4847-8807
Asmita SamadderCytogenetics and Molecular Biology Lab., Department of Zoology, University of Kalyani, Kalyani, Nadia, 741235, India.ORCID 0000-0002-3604-7404
Sisir NandiGlobal Institute of Pharmaceutical Education and Research (Affiliated to Veer Madho Singh Bhandari Uttarakhand Technical University), Kashipur, 244713, India.ORCID 0000-0002-9960-6584
University of Kalyani · INUttarakhand Technical University · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTrypanosomiasis, caused by protozoan parasites of the

introductionThis review article aims to provide a comprehensive overview of the role of cysteine proteases in trypanosomiasis and their potential as therapeutic targets. We discuss the biological significance of cysteine proteases in

methodsA comprehensive literature search was conducted to identify relevant studies and research articles on the role of cysteine proteases and their inhibitors in trypanosomiasis. The selected studies were critically analyzed to extract key findings and provide a comprehensive overview of the topic.

resultsCysteine proteases, such as cruzipain, TbCatB and TbCatL, have been identified as promising therapeutic targets due to their essential roles in

conclusionTargeting cysteine proteases and their inhibitors holds great potential for the development of novel antiparasitic drugs against trypanosomiasis. The identification of potent and selective cysteine protease inhibitors could significantly contribute to the combat against trypanosomiasis and improve the prospects for the treatment of this neglected tropical disease.

Indexed as

Cysteine ProteasesCysteine Proteinase InhibitorsTrypanosomaTrypanosomiasisAnimalsHumansProtozoan ProteinsTrypanocidal AgentsCysteine ProteasesCysteine Proteinase InhibitorsProtozoan ProteinsTrypanocidal Agentscathepsin B (TbCatB).cruzaincysteine protease inhibitorsrhodesain (TbCatL)Trypanosoma bruceiTrypanosoma cruziTrypanosomiasis

Identifiers

PMID37340748
OpenAlexW4381470210

What Socratic 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 Socratic graph.