Evidence map›Paper›PMID 37480422›Full record

ArticleMolecular diversity2024

In-vitro antiviral activity and in-silico targeted study of quinoline-3-carboxylate derivatives against SARS-Cov-2 isolate.

Ravi Kumar Mittal, Priyank Purohit, Murugesan Sankaranarayanan, Mohammed Muzaffar-Ur-Rehman, Donatella Taramelli, Lucia Signorini, Maria Dolci, Nicoletta Basilico

Abstract read
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In one paragraph

Article in Molecular diversity, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
–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

9 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Recent Advances in Nitrogen-Containing Heterocyclic Scaffolds as Antiviral Agents.Medicinal chemistry (Shariqah (United Arab Emirates)) · 2024
    Pooled it
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  9. Nitrogen-fused Heterocycles: Empowering Anticancer Drug Discovery.Medicinal chemistry (Shariqah (United Arab Emirates)) · 2024
    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

8 authors.

Ravi Kumar MittalNational Institute of Pharmaceutical Education and Research, S A S Nagar Mohali, Punjab, 160062, India.
Priyank PurohitSchool of Pharmacy, Graphic Era Hill University, Dehradun, Uttarakhand, 248002, India. priyank.niper@gmail.com.
Murugesan SankaranarayananMedicinal Chemistry Research Laboratory, Department of Pharmacy, BITS Pilani, Pilani Campus, Pilani, Rajasthan, 333031, India.
Mohammed Muzaffar-Ur-RehmanMedicinal Chemistry Research Laboratory, Department of Pharmacy, BITS Pilani, Pilani Campus, Pilani, Rajasthan, 333031, India.
Donatella TaramelliDepartment of Pharmacological and Biomolecular Sciences, University of Milan, Pascal Street 36, 20133, Milan, Italy.
Lucia SignoriniDepartment of Biomedical, Surgical and Dental Sciences, University of Milan, Pascal Street 36, 20133, Milan, Italy.
Maria DolciDepartment of Biomedical, Surgical and Dental Sciences, University of Milan, Pascal Street 36, 20133, Milan, Italy.
Nicoletta BasilicoDepartment of Biomedical, Surgical and Dental Sciences, University of Milan, Pascal Street 36, 20133, Milan, Italy.

Funding

Department of Biotechnology, Ministry of Science and Technology, India BT/PR5634/MED/29/623/2012Dipartimento di Medicina e Chirurgia, Università degli Studi di Milano-Bicocca PSR2019ICMR- National Institute of Virology 5/7/827/12-RCH
6 · The paper itself

Abstract

In recent years, the viral outbreak named COVID-19 showed that infectious diseases have a huge impact on both global health and the financial and economic sectors. The lack of efficacious antiviral drugs worsened the health problem. Based on our previous experience, we investigated in vitro and in silico a series of quinoline-3-carboxylate derivatives against a SARS-CoV-2 isolate. In the present study, the in-vitro antiviral activity of a series of quinoline-3-carboxylate compounds and the in silico target-based molecular dynamics (MD) and metabolic studies are reported. The compounds' activity against SARS-CoV-2 was evaluated using plaque assay and RT-qPCR. Moreover, from the docking scores, it appears that the most active compounds (1j and 1o) exhibit stronger binding affinity to the primary viral protease (NSP5) and the exoribonuclease domain of non structural protein 14 (NSP14). Additionally, the in-silico metabolic analysis of 1j and 1o defines CYP2C9 and CYP3A4 as the major P450 enzymes involved in their metabolism.

Indexed as

Antiviral AgentsMolecular Docking SimulationMolecular Dynamics SimulationQuinolinesSARS-CoV-2AnimalsChlorocebus aethiopsComputer SimulationCoronavirus 3C ProteasesCOVID-19COVID-19 Drug TreatmentHumansVero CellsAntiviral AgentsCoronavirus 3C ProteasesQuinolinesAnti-viral drugsMolecular dynamicsProtease inhibitorsSARS-CoV-2Targeted anti-viral

Identifiers

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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.