Evidence map›Paper›PMID 39773044›Full record

ReviewCurrent medicinal chemistry2025

Advancements in Structural Basis of Covalent Inhibitors Targeting SARS-CoV-2 Essential Proteins.

Israr Fatima, Fahad M Alshabrmi, Faris F Aba Alkhayl, Muhammad Qasim, Almera Shafqat, Sara Batool, Muhammad Jawad, Muhammad Tahir Ul Qamar, Abdur Rehman

Abstract readReview
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In one paragraph

Review in Current medicinal chemistry, 2025. 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

9 authors.

Israr FatimaCenter of Bioinformatics, College of Life Sciences, Northwest Agriculture and Forestry University, Yangling, China.
Fahad M AlshabrmiDepartment of Medical Laboratories, College of Applied Medical Sciences, Qassim University, Buraydah, 51452, Saudi Arabia.
Faris F Aba AlkhaylDepartment of Medical Laboratories, College of Applied Medical Sciences, Qassim University, Buraydah, 51452, Saudi Arabia.
Muhammad QasimDepartment of Bioinformatics and Biotechnology, Government College University Faisalabad, Faisalabad, Pakistan.
Almera ShafqatDepartment of Bioinformatics and Biotechnology, Government College University Faisalabad, Faisalabad, Pakistan.
Sara BatoolDepartment of Bioinformatics and Biotechnology, Government College University Faisalabad, Faisalabad, Pakistan.
Muhammad JawadDepartment of Bioinformatics and Biotechnology, Government College University Faisalabad, Faisalabad, Pakistan.
Muhammad Tahir Ul QamarDepartment of Bioinformatics and Biotechnology, Government College University Faisalabad, Faisalabad, Pakistan.
Abdur RehmanCenter of Bioinformatics, College of Life Sciences, Northwest Agriculture and Forestry University, Yangling, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Covalent inhibitors play a pivotal role in the development of pharmaceutical therapies, as they form stable, irreversible bonds with target biomolecules, leading to prolonged therapeutic effects and enhanced efficacy. Since covalent inhibitors first appeared in the late 1800s, the field has become innovative rapidly, and covalent inhibitors now account for around 30% of all marketed therapeutics. The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) causes the pandemic of coronavirus disease 2019 (COVID-19). SARS-CoV-2 needs to be cured with a medicine that is beneficial and with the least side effects. It is necessary to formulate drug candidates to treat this pathogen. The predominance of covalent medications will be briefly discussed in this review, followed by an introduction to their methods of action, as well as more thorough discussions of the safe and effective covalent enzyme inhibitors against SARS-CoV-2. Our main concern is to study covalent inhibitors which are mainly involved in blocking the viral entry of the virus SARS-CoV-2 into the host cell along with its replication and translation process. In the development of anti-SARS-CoV-2 medicines researchers can use those reported drugs as prospective candidates.

Indexed as

Antiviral AgentsCOVID-19 Drug TreatmentSARS-CoV-2Coronavirus 3C ProteasesCOVID-19HumansVirus InternalizationAntiviral AgentsCoronavirus 3C Proteasescomputer aided drug designingcovalent inhibitorscovalent inhibitors.molecular docking simulationnatural productsSevere acute respiratory syndrome coronavirus 2 (SARS-CoV-2)

Identifiers

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.