Evidence map›Paper›PMID 41108185›Full record

ReviewFuture medicinal chemistry2025

Advanced cancer therapy: unlocking the potential of small molecule inhibitors.

Siuli Sen, Dipanjan Karati

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 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

2 authors.

Siuli SenDepartment of Pharmaceutical Technology, School of Pharmacy, Techno India University, Kolkata, West Bengal, India.ORCID 0009-0006-0927-6195
Dipanjan KaratiDepartment of Pharmaceutical Technology, School of Pharmacy, Techno India University, Kolkata, West Bengal, India.ORCID 0000-0003-0734-6015

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionCancer is one of the predominant causes of mortality globally. Radiation, surgery, and chemotherapy are currently available methods for treating cancer. Each of these approaches has known adverse effects. Due to their better efficacy and safety over traditional chemotherapy drugs, targeted therapeutic medicines are quickly becoming standard cancer treatments. AREAS COVERED: Small molecules have several advantages, such as being able to be given orally and having the capacity to pass through cell membranes and enter intracellular spaces. This review is going to focus on small molecules as anticancer scaffolds and researchers will be able to design new antineoplastic compounds in the future on the basis of the thoroughly discussed SAR investigation, preclinical data, clinical outcomes, and FDA approved molecules. EXPERT OPINION: Since there is currently no cure for most forms of disseminated cancer, the development of novel active chemotherapeutic drugs is essential. Small molecules are interesting drug candidates as they are able to target important molecular pathways with selectivity. An in-depth analysis of the SAR study and the available preclinical and clinical data can greatly assist in the development of the next generation of anticancer drugs that would be more potent, selective, and would interfere with fewer side effects.

Indexed as

Antineoplastic AgentsNeoplasmsSmall Molecule LibrariesAnimalsHumansStructure-Activity RelationshipAntineoplastic AgentsSmall Molecule LibrariesanticancerepigeneticKinaseSAR studySmall molecules

Identifiers

PMID41108185
PMCPMC12582126

What OpenQuestion 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 OpenQuestion graph.