Evidence map›Paper›PMID 41226260›Full record

ReviewMolecules (Basel, Switzerland)2025

Advances in Naturally and Synthetically Derived Bioactive Sesquiterpenes and Their Derivatives: Applications in Targeting Cancer and Neurodegenerative Diseases.

Liana R Cutter, Alexandra R Ren, Ipsita A Banerjee

Abstract readReview
In one paragraph

Review in Molecules (Basel, Switzerland), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Review
  3. Synthesis of α-Santonin Derivatives Linked toAntibiotics (Basel, Switzerland) · 2026
    Article
  4. Article
  5. 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.

Liana R CutterDepartment of Chemistry and Biochemistry, Fordham University, 441 East Fordham Road, Bronx, New York, NY 10458, USA.ORCID 0009-0001-2159-9177
Alexandra R RenDepartment of Chemistry and Biochemistry, Fordham University, 441 East Fordham Road, Bronx, New York, NY 10458, USA.ORCID 0009-0003-1759-7106
Ipsita A BanerjeeDepartment of Chemistry and Biochemistry, Fordham University, 441 East Fordham Road, Bronx, New York, NY 10458, USA.ORCID 0000-0002-6987-9717

Funding

Fordham University N/AHenry Luce Foundation N/A
6 · The paper itself

Abstract

Sesquiterpenes are a diverse class of natural products that have garnered considerable interest for their potent bioactivity and structural variability. This review highlights advances in the derivatization of various sesquiterpene lactones, quinones, and alcohols, particularly in targeting cancer and neurodegenerative diseases. The structural modifications discussed include the incorporation of triazole, arylidene, or thiol moieties with eudesmane, guaiane, and germacranolide-type sesquiterpenes, among others. In addition, the conjugation with chemotherapeutics, as well as the development of nanoscale therapeutics, is also discussed. Such modifications have expanded the pharmacological potential, enabling improved specificity, cytotoxicity profiles, and sensitization toward tumor cells. Additionally, sesquiterpenes such as parthenolide (

Indexed as

Antineoplastic AgentsBiological ProductsNeoplasmsNeurodegenerative DiseasesSesquiterpenesAnimalsAntioxidantsHumansAntineoplastic AgentsAntioxidantsBiological ProductsSesquiterpenesconjugatesnanotherapeuticssesquiterpene lactonessesquiterpene quinonessesquiterpenes

Identifiers

PMID41226260
PMCPMC12609730

What Socratic holds

Textmetadata
LicenceCC BY
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.