Evidence map›Paper›PMID 41510714›Full record

ReviewMini reviews in medicinal chemistry2026

Recent Developments in Heterocyclic Derivatives as Novel Cancer Therapeutics: From 2020-2024.

Sucheta Singh, Hrithik Dey, Meenakshi Kaira, Kailash C Pandey, Sumit Tahlan

Abstract readReview
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In one paragraph

Review in Mini reviews in medicinal chemistry, 2026. 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

5 authors.

Sucheta SinghDepartment of Pharmaceutical Sciences, Maharshi Dayanand University, Rohtak, 124001, India.
Hrithik DeyLloyd Institute of Management and Technology, Plot No.-11, Knowledge Park-II, Greater Noida, Uttar Pradesh, 201306, India.
Meenakshi KairaLloyd Institute of Management and Technology, Plot No.-11, Knowledge Park-II, Greater Noida, Uttar Pradesh, 201306, India.
Kailash C PandeyICMR National Institute of Malaria Research, New Delhi, 11007, India.
Sumit TahlanICMR National Institute of Malaria Research, New Delhi, 11007, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite progress in cancer research, cancer continues to be a leading cause of mortality worldwide; hence, therapeutic strategies must constantly improve. Drug discovery has revealed that heterocyclic moieties are fundamental and unique scaffolds because of their structural versatility and ability to interact with key biological targets. In these cyclic compounds, heteroatoms are a signature that serves to modulate cellular pathways relevant to tumor progression, apoptosis, and proliferation. Hybridization between the aromatic ring and the non-aromatic ring in a heterocyclic structure has resulted in the development of novel heterocyclic derivatives with increased anticancer activity, increased selectivity, and reduced adverse effects in the clinic, and has recently been used extensively in medicinal chemistry. Research has been directed towards the improvement of their molecular frameworks and integration of computational modelling for drug design, as well as advanced drug delivery systems to improve their therapeutic potential. As this field is progressing rapidly, this review attempts to comprehensively analyze the role of heterocyclic moieties in the development of anticancer drugs, the latest advances, and prospects. This study will contribute to ongoing efforts to design more effective and targeted cancer therapies by summarizing key findings and emerging trends.

Indexed as

Antineoplastic AgentsHeterocyclic CompoundsNeoplasmsAnimalsApoptosisCell ProliferationHumansMolecular StructureAntineoplastic AgentsHeterocyclic Compoundsanticancer agentscancercell linesHeterocyclic scaffoldsleukaemiaSAR

Identifiers

PMID41510714

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.