Evidence map›Paper›PMID 40567473›Full record

ReviewRSC advances2025

From molecule to medicine: introducing emerging strategies to synthesize potent anticancer purine scaffolds.

Muhammad Aown Hashmi, Aqsa Kanwal, Umme Habibah Siddiqua, Nasir Rasool, Ayesha Malik

Abstract readReview
In one paragraph

Review in RSC advances, 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

5 authors.

Muhammad Aown HashmiDepartment of Chemistry, Government College University Faisalabad Faisalabad 38000 Pakistan drayeshamalik@gcuf.edu.pk.
Aqsa KanwalDepartment of Chemistry, Government College University Faisalabad Faisalabad 38000 Pakistan drayeshamalik@gcuf.edu.pk.
Umme Habibah SiddiquaDepartment of Chemistry, University of Jhang Jhang Pakistan u.habibah5@gmail.com.
Nasir RasoolDepartment of Chemistry, Government College University Faisalabad Faisalabad 38000 Pakistan drayeshamalik@gcuf.edu.pk.
Ayesha MalikDepartment of Chemistry, Government College University Faisalabad Faisalabad 38000 Pakistan drayeshamalik@gcuf.edu.pk.ORCID https://orcid.org/0009-0005-5748-1188

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer remains a major global health concern, necessitating the continuous development of novel anticancer agents with enhanced efficacy and reduced side effects. Purine derivatives are privileged bioactive scaffolds that play a crucial role in drug discovery due to their presence in essential biomolecules such as DNA, RNA, ATP, and coenzymes. This review highlights the synthesis, structure-activity relationships (SARs), and anticancer evaluations of various purine hybrids, including aryl piperazine, triazole-hybrid piperidine/pyrrolidine, and diazenyl-containing purines, from 2020 to 2024. Hybrid molecules incorporating chalcones, thiazoles, thiazolidinones, xanthine, and bis-purine linkers have expanded the therapeutic landscape of purine-based anticancer agents. Comparative analyses of IC

Identifiers

PMID40567473
PMCPMC12188300

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.