Evidence map›Paper›PMID 40497671›Full record

ReviewFuture medicinal chemistry2025

Pyrimidine hybrids with

Junna Liu, Xiaoyan Zhang, Yafei Zhuang, Zhi Xu, Wei Zhou

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. Review
  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.

Junna LiuSchool of Pharmacy, Guizhou Medical University, Guiyang, China.
Xiaoyan ZhangSchool of Basic Medicine, Guizhou Medical University, Guiyang, China.
Yafei ZhuangSchool of Pharmacy, Hubei University of Science and Technology, Xianning, China.
Zhi XuSchool of Pharmacy, Guizhou Medical University, Guiyang, China.
Wei ZhouSchool of Pharmacy, Guizhou Medical University, Guiyang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chemotherapy has transformed cancer from a catastrophic disease to a treatable and sometimes curable disease, but multidrug resistance is a predominant obstacle to effective chemotherapy, creating an urgent demand to explore novel anticancer therapeutics. Pyrimidine is necessary to maintain cellular fundamental function and is critical in cancer cell proliferation as well as survival, and some pyrimidine-based agents have been developed as anticancer therapeutics. In particular, pyrimidine hybrids can act on distinct biological targets in cancer cells simultaneously and have potential advantages in increasing anticancer therapeutic efficacy and circumventing drug resistance, indicating that the rational design of pyrimidine hybrids may provide valuable therapeutic interventions for cancer therapy. This review outlines the current scenario of the

Indexed as

Antineoplastic AgentsNeoplasmsPyrimidinesAnimalsCell ProliferationHumansAntineoplastic AgentspyrimidinePyrimidinesanticancer activityhybrid moleculesin vivo efficacymechanisms of actionPyrimidine

Identifiers

PMID40497671
PMCPMC12296079

What Socratic 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 Socratic graph.