Evidence map›Paper›PMID 40874642›Full record

ReviewFuture medicinal chemistry2025

Thiazole derivatives in cancer therapy: mechanistic insights, bioactivity, and future perspective.

Honey Saini, Anuradha Mehra, Amit Mittal

Abstract readReview
In one paragraph

Review in Future medicinal chemistry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

3 authors.

Honey SainiDepartment of Pharmaceutical Chemistry, School of Pharmaceutical Sciences, Lovely Professional University, Phagwara, India.
Anuradha MehraDepartment of Pharmaceutical Chemistry, School of Pharmaceutical Sciences, Lovely Professional University, Phagwara, India.ORCID 0000-0002-7405-8809
Amit MittalDepartment of Pharmaceutical Chemistry, School of Pharmaceutical Sciences, Lovely Professional University, Phagwara, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Globally, cancer is the primary cause of both mortality and morbidity. Many researchers are working to create new anticancer drugs that are less harmful and more effective. A thiazole scaffold is a great option for developing compounds that interact with cancer target locations and block the biological pathways causing the disease to spread. The current state of thiazole-based anticancer medicines is highlighted in this review, along with recent research findings. The thiazole moiety is an eccentric building block for creating anticancer medications. Thiazole derivatives have a great pharmacological profile that targets a variety of proteins and enzymes. The thiazoles are highlighted by the nitrogen atom's ability to establish hydrogen bonds with their targets. Thiazole has been shown in numerous clinical trials to be useful in treating cancer by acting through a variety of routes. Research on thiazole derivatives for cancer treatment featuring a superior pharmacokinetic profile is encouraged by the approval of thiazole-based medications for use as chemotherapeutics, such as Dasatinib and Ixazomib. This led to the consideration of thiazole derivatives as anticancer drugs to identify possible derivatives that are currently being investigated. This review covers research on thiazole scaffolds with anti-cancer potential both

Indexed as

Antineoplastic AgentsNeoplasmsThiazolesAnimalsHumansAntineoplastic AgentsThiazolesapoptosiscancerderivativesinhibitorSARThiazole

Identifiers

PMID40874642
PMCPMC12407936

What OpenQuestion holds

Textmetadata
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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.