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ReviewMedicinal chemistry (Shariqah (United Arab Emirates))2025

Pharmacological Evaluation of Bioisosterically Replaced and Triazole- Tethered Derivatives for Anticancer Therapy.

Dipesh Kumar, Salahuddin, Avijit Mazumder, Rajnish Kumar, Mohamed Jawed Ahsan, Mohammad Shahar Yar, Abbussalam, Pankaj Kumar Tyagi, M V N L Chaitanya

Abstract readReview
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In one paragraph

Review in Medicinal chemistry (Shariqah (United Arab Emirates)), 2025. 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
–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

3 citing papers in PubMed.

  1. Review
  2. 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.

Dipesh KumarDepartment of Pharmaceutical Chemistry, Noida Institute of Engineering and Technology (Pharmacy Institute), Plot no. 19, Knowledge Park-2, Greater Noida, 201306, Uttar Pradesh, India.
SalahuddinDepartment of Pharmaceutical Chemistry, Noida Institute of Engineering and Technology (Pharmacy Institute), Plot no. 19, Knowledge Park-2, Greater Noida, 201306, Uttar Pradesh, India.
Avijit MazumderDepartment of Pharmaceutical Chemistry, Noida Institute of Engineering and Technology (Pharmacy Institute), Plot no. 19, Knowledge Park-2, Greater Noida, 201306, Uttar Pradesh, India.
Rajnish KumarDepartment of Pharmaceutical Chemistry, Noida Institute of Engineering and Technology (Pharmacy Institute), Plot no. 19, Knowledge Park-2, Greater Noida, 201306, Uttar Pradesh, India.
Mohamed Jawed AhsanDepartment of Pharmaceutical Chemistry, Faculty of Pharmacy, Jahangirabad Institute of Technology, Jahangirabad Fort, Jahangirabad, Barabanki Uttar Pradesh, 225203, India.
Mohammad Shahar YarDepartment of Pharmaceutical Chemistry, School of Pharmaceutical Education and Research, Jamia Hamdard University, Hamdard Nagar, New Delhi, 110062, India.
AbbussalamDepartment of Physiology, Era's Lucknow Medical College and Hospital, Lucknow, 226003, India.
Pankaj Kumar TyagiDepartment of Biotechnology, Noida Institute of Engineering and Technology, Plot No.19, Knowledge Park-2, Greater Noida, 201306, Uttar Pradesh, India.
M V N L ChaitanyaSchool of Pharmaceutical Sciences, Lovely Professional University, Phagwara, Punjab, 144411, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer has been the cause of the highest number of deaths in the human population despite the development and advancement in treatment therapies. The toxicity, drug resistance, and side effects of the current medicaments and therapies have left the void for more research and development. One of the possibilities to fill this void is by incorporating Triazole moieties within existing anticancer pharmacophores to develop new hybrid drugs with less toxicity and more potency. The placement of nitrogen in the triazole ring has endowed its characterization of being integrated with anticancer pharmacophores via bioisosteric replacement, click chemistry and organocatalyzed approaches. This review paper emphasizes the discussions from articles published from the early 2000s to the current 2020s about the triazole-based derivatives used in anticancer therapy, elaborating more on their chemical structures, target receptors or enzymes, mechanism of action, structure-activity relationships, different triazole-derived hybrid drugs under clinical and nonclinical trials, and recent advancements toward developing more potent and less toxic anticancer agents.

Indexed as

Antineoplastic AgentsNeoplasmsTriazolesDrug Screening Assays, AntitumorHumansMolecular StructureStructure-Activity RelationshipAntineoplastic AgentsTriazolesAnticancer pharmacophoresbioisosteric replacementcarcinomic cellsdrug developmenthybrid drugstriazoletriazole-tethered.

Identifiers

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Registered trials

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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.