Evidence map›Paper›PMID 40076268›Full record

ReviewMolecules (Basel, Switzerland)2025

Synthetic Approaches to Novel DPP-IV Inhibitors-A Literature Review.

Valentin Petrov, Teodora Aleksandrova, Aleksandar Pashev

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 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

3 authors.

Valentin PetrovDepartment of Chemistry and Biochemistry, Faculty of Pharmacy, Medical University-Pleven, 1 St. Kliment Ohridski Str., 5800 Pleven, Bulgaria.
Teodora AleksandrovaDepartment of Chemistry and Biochemistry, Faculty of Pharmacy, Medical University-Pleven, 1 St. Kliment Ohridski Str., 5800 Pleven, Bulgaria.
Aleksandar PashevDepartment of Chemistry and Biochemistry, Faculty of Pharmacy, Medical University-Pleven, 1 St. Kliment Ohridski Str., 5800 Pleven, Bulgaria.ORCID 0000-0002-0303-9053

Funding

European Union-NextGenerationEU, through the National Recovery and Resilience Plan of the Republic of Bulgaria, project № BG-RRP-2.004-0003 BG-RRP-2.004-0003
6 · The paper itself

Abstract

Dipeptidyl peptidase IV (DPP-IV) is a serine protease whose inhibition has been an object of considerable interest in the context of developing novel treatments for type 2 diabetes mellitus. The development of novel DPP-IV inhibitors from natural or synthetic origin has seen a growing scientific interest in recent years, especially during the SARS-CoV-2 pandemic, when DPP-IV inhibitors were found to be of beneficial therapeutic value for COVID-19 patients. The present manuscript aims to summarize the most recent information on the synthesis of different DPP-IV inhibitors, emphasizing the various heterocyclic scaffolds that can be found in them. Special attention is devoted to DPP-IV inhibitors that are currently in clinical trials. Different synthetic approaches for the construction of DPP-IV inhibitors are discussed, as well as the most recent developments in the field.

Indexed as

COVID-19 Drug TreatmentDipeptidyl-Peptidase IV InhibitorsCOVID-19Diabetes Mellitus, Type 2Dipeptidyl Peptidase 4HumansHypoglycemic AgentsSARS-CoV-2Dipeptidyl Peptidase 4Dipeptidyl-Peptidase IV InhibitorsHypoglycemic AgentsDPP-IV inhibitorsdrug designheterocyclic synthesismedicinal chemistrytype 2 diabetes

Identifiers

PMID40076268
PMCPMC11902039

What OpenQuestion holds

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Registered trials

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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.