Evidence map›Paper›PMID 38185891›Full record

ReviewMini reviews in medicinal chemistry2024

Quinoline Derivatives as Promising Scaffolds for Antitubercular Activity: A Comprehensive Review.

Mohammad Owais, Arun Kumar, Syed Misbahul Hasan, Kuldeep Singh, Iqbal Azad, Arshad Hussain, Suvaiv, Mohd Akil

Abstract readReview
PubMed Publisher
In one paragraph

Review in Mini reviews in medicinal chemistry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
4.5field-weighted citation impact, top 5% 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

6 citing papers in PubMed, 18 citations in OpenAlex.

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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 at 1 institution in 1 country.

Mohammad OwaisFaculty of Pharmacy, Integral University, Kursi Road, Lucknow 226026 (U.P.), India.
Arun KumarFaculty of Pharmacy, Integral University, Kursi Road, Lucknow 226026 (U.P.), India.
Syed Misbahul HasanFaculty of Pharmacy, Integral University, Kursi Road, Lucknow 226026 (U.P.), India.
Kuldeep SinghFaculty of Pharmacy, Integral University, Kursi Road, Lucknow 226026 (U.P.), India.
Iqbal AzadDepartment of Chemistry, Integral University, Kursi Road, Lucknow 226026 (U.P.), India.
Arshad HussainHarsha Institute of Pharmacy, Itaunja, Lucknow 226203, (U.P.), India.
SuvaivFaculty of Pharmacy, Integral University, Kursi Road, Lucknow 226026 (U.P.), India.
Mohd AkilDepartment of Chemistry, Integral University, Kursi Road, Lucknow 226026 (U.P.), India.
Integral University · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHeterocyclic compounds and their derivatives play a significant role in the design and development of novel quinoline drugs. Among the various pharmacologically active heterocyclic compounds, quinolines stand out as the most significant rings due to their broad pharmacological roles, specifically antitubercular activity, and their presence in plant-based compounds. Quinoline is also known as benzpyridine, benzopyridine, and 1-azanaphthalene. It has a benzene ring fused with a pyridine ring, and both rings share two carbon atoms. The importance of quinoline lies in its incorporation as a key component in various natural compounds found in medicinal plant families like

objectiveThis article is expected to have a significant impact on the advancement of effective antitubercular drugs. Through harnessing the potent activity of quinoline derivatives, the research aims to make valuable contributions to combating tuberculosis more efficiently and ultimately reducing the global burden of this infectious disease.

methodsNumerous nitrogen-containing heterocyclic compounds exhibit significant potential as antitubercular agents. These chemicals have fused aromatic nitrogen-heterocyclic nuclei that can change the number of electrons they have, which can change their chemical, physical, and biological properties. This versatility comes from their ability to bind with the receptors in multiple modes, a critical aspect of drug pharmacological screening. Among these compounds, quinoline stands out as it incorporates a stable fusion of a benzene ring with a pyridine nucleus. Quinolines have demonstrated a diverse range of pharmacological activities, including but not limited to anti-tubercular, anti-tumor, anticoagulant, anti-inflammatory, antioxidant, antiviral, antimalarial, anti-HIV, and antimicrobial effects.

resultsSome molecules, such as lone-paired nitrogen species, include pyrrole, pyrazole, and quinoline. These molecules contain nitrogen and take part in metabolic reactions with other molecules inside the cell. However, an excessive accumulation of reactive nitrogen species can lead to cytotoxicity, resulting in damage to essential biological macromolecules. Among these compounds, quinoline stands out as the oldest and most effective one, exhibiting a wide range of significant properties such as antitubercular, antimicrobial, anti-inflammatory, antioxidant, analgesic, and anticonvulsant activities. Notably, naturally occurring quinoline compounds, such as quinine, have proven to be potent antimalarial drugs.

conclusionThis review highlights quinoline derivatives' antitubercular potential, emphasizing recent research advancements. Utilizing IC

Indexed as

Antitubercular AgentsQuinolinesAnimalsHumansMicrobial Sensitivity TestsMolecular StructureMycobacterium tuberculosisAntitubercular AgentsQuinolinesheterocyclic compoundsHIVisoniazid.mycobacterium tuberculosisquinolineTuberculosis

Identifiers

PMID38185891
OpenAlexW4390664714

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.