Evidence map›Paper›PMID 38343054›Full record

ReviewCurrent pharmaceutical design2024

2,5-Diketopiperazines (DKPs): Promising Scaffolds for Anticancer Agents.

Shaimaa S Goher, Wessam S Abdrabo, Giri Babu Veerakanellore, Bahaa Elgendy

Abstract readReview
PubMed Publisher
In one paragraph

Review in Current pharmaceutical design, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. 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

4 authors.

Shaimaa S GoherChemistry Department, Faculty of Science, Benha University, Benha 13518, Egypt.ORCID 0000-0002-0126-7896
Wessam S AbdraboChemistry Department, Faculty of Science, Benha University, Benha 13518, Egypt.ORCID 0000-0001-8210-8346
Giri Babu VeerakanelloreCenter for Clinical Pharmacology, Washington University School of Medicine and University of Health Sciences and Pharmacy, St. Louis, Missouri 63110, United States.ORCID 0000-0002-8866-3882
Bahaa ElgendyChemistry Department, Faculty of Science, Benha University, Benha 13518, Egypt.ORCID 0000-0003-4800-7976

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

2,5-Diketopiperazine (2,5-DKP) derivatives represent a family of secondary metabolites widely produced by bacteria, fungi, plants, animals, and marine organisms. Many natural products with DKP scaffolds exhibited various pharmacological activities such as antiviral, antifungal, antibacterial, and antitumor. 2,5-DKPs are recognized as privileged structures in medicinal chemistry, and compounds that incorporate the 2,5-DKP scaffold have been extensively investigated for their anticancer properties. This review is a thorough update on the anti-cancer activity of natural and synthesized 2,5-DKPs from 1997 to 2022. We have explored various aspects of 2,5-DKPs modifications and summarized their structure-activity relationships (SARs) to gain insight into their anticancer activities. We have also highlighted the novel approaches to enhance the specificity and pharmacokinetics of 2,5-DKP-based anticancer agents.

Indexed as

Antineoplastic AgentsDiketopiperazinesAnimalsBiological ProductsCell ProliferationHumansMolecular StructureNeoplasmsStructure-Activity RelationshipAntineoplastic AgentsBiological ProductsDiketopiperazines25-Diketopiperazines (25-DKPs)anticancer activitiesmarine fungusnatural alkaloidsnatural productspharmacological activities.

Identifiers

PMID38343054

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.