Evidence map›Paper›PMID 39318218›Full record

ReviewAnti-cancer agents in medicinal chemistry2025

Acyl Urea Compounds Therapeutics and its Inhibition for Cancers in Women: A Review.

Preeti Kumari, Rakhi Mishra, Rupa Mazumder, Avijit Mazumder

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In one paragraph

Review in Anti-cancer agents in medicinal chemistry, 2025. 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

4 authors.

Preeti KumariNoida Institute of Engineering and Technology (Pharmacy Institute), Greater Noida, 201306, India.
Rakhi MishraNoida Institute of Engineering and Technology (Pharmacy Institute), Greater Noida, 201306, India.ORCID 0000-0002-9292-3448
Rupa MazumderNoida Institute of Engineering and Technology (Pharmacy Institute), Greater Noida, 201306, India.
Avijit MazumderNoida Institute of Engineering and Technology (Pharmacy Institute), Greater Noida, 201306, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acyl urea compounds have garnered significant attention in cancer therapeutics, particularly for their potential effectiveness against cancers that predominantly affect women, such as breast and ovarian cancers. The paper presents a report on the investigation of acyl urea compounds that are reported to involve a multi-faceted approach, including synthetic chemistry, biological assays, and computational modeling. A wealth of information on acyl urea and its purported effects on cancer affecting women has been gathered from different sources and condensed to provide readers with a broad understanding of the role of acyl urea in combating cancer. Acylureas demonstrate promising results by selectively inhibiting key molecular targets associated with cancer progressions, such as EGFR, ALK, HER2, and the Wnt/β-catenin signaling pathway. Specifically, targeting acyl ureas impedes tumor proliferation and metastasis while minimizing harm to healthy tissues, offering a targeted therapeutic approach with reduced side effects compared to conventional chemotherapy. Continued research and clinical trials are imperative to optimize the efficacy and safety profiles of acylurea-based therapies and broaden their applicability across various cancer types. Acyl urea compounds represent a promising class of therapeutics for the treatment of cancers in women, particularly due to their ability to selectively inhibit key molecular targets involved in tumor growth and progression. The combination of synthetic optimization, biological evaluation, and computational modeling has facilitated the identification of several lead compounds with significant anticancer potential. This abstract explores the therapeutic mechanisms and targeted pathways of acyl ureas in combating these malignancies, which will be useful for future studies.

Indexed as

Antineoplastic AgentsBreast NeoplasmsUreaCell ProliferationDrug Screening Assays, AntitumorFemaleHumansMolecular StructureStructure-Activity RelationshipAntineoplastic AgentsUreaAcylureabreast cancer.chemotherapycolorectal cancersignaling pathwaystargets

Identifiers

PMID39318218

What OpenQuestion holds

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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.