Evidence map›Paper›PMID 35408660›Full record

ArticleMolecules (Basel, Switzerland)2022

Discovery of Novel Epoxyketone Peptides as Lipase Inhibitors.

Jehad Almaliti, Muhammed Alzweiri, Momen Alhindy, Tamam Al-Helo, Ibrahim Daoud, Raghad Deknash, C Benjamin Naman, Bashaer Abu-Irmaileh, Yasser Bustanji, Islam Hamad

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.0field-weighted citation impact, top 25% of its field
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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Review
  3. 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

10 authors at 3 institutions in 4 countries.

Jehad AlmalitiDepartment Pharmaceutical Sciences, College of Pharmacy, The University of Jordan, Amman 11942, Jordan.
Muhammed AlzweiriDepartment Pharmaceutical Sciences, College of Pharmacy, The University of Jordan, Amman 11942, Jordan.ORCID 0000-0003-3473-2552
Momen AlhindyDepartment Pharmaceutical Sciences, College of Pharmacy, The University of Jordan, Amman 11942, Jordan.
Tamam Al-HeloDepartment Pharmaceutical Sciences, College of Pharmacy, The University of Jordan, Amman 11942, Jordan.ORCID 0000-0002-7776-6616
Ibrahim DaoudDepartment Pharmaceutical Sciences, College of Pharmacy, The University of Jordan, Amman 11942, Jordan.
Raghad DeknashDepartment Pharmaceutical Sciences, College of Pharmacy, The University of Jordan, Amman 11942, Jordan.
C Benjamin NamanLi Dak Sum Yip Yio Chin Kenneth Li Marine Biopharmaceutical Research Center, Department of Marine Pharmacy, College of Food and Pharmaceutical Sciences, Ningbo University, Ningbo 315800, China.ORCID 0000-0002-4361-506X
Bashaer Abu-IrmailehHamdi Mango Center for Scientific Research, The University of Jordan, Amman 11942, Jordan.
Yasser BustanjiDepartment Pharmaceutical Sciences, College of Pharmacy, The University of Jordan, Amman 11942, Jordan.
Islam HamadDepartment of Pharmacy, Faculty of Health Sciences, American University of Madaba, Madaba 11821, Jordan.
University of Jordan · JOAmerican University of Madaba · JONingbo University · CN

Funding

King Abdullah II Fund For Development (KAFD) 2020/10the university of Jordan 2021-66/2020
6 · The paper itself

Abstract

Obesity is the most common nutritional disorder in the developed world and is associated with important comorbidities. Pancreatic lipase (PL) inhibitors play a key role in the metabolism of human fat. A series of novel epoxyketones peptide derivatives were investigated for their pancreatic lipase inhibitory activity. The epoxyketone moiety is a well-known reactive electrophile group that has been used as part of proteasome inhibitors in cancer therapy, and it is widely believed that these are very selective for targeting the proteasome active site. Here we investigated various peptide derivatives with an epoxide warhead for their anti-lipase activity. The assessment of these novel epoxyketones was performed by an in-house method that we developed for rapid screening and identification of lipase inhibitors using GC-FID. Herein, we present a novel anti-lipase pharmacophore based on epoxyketone peptide derivatives that showed potent anti-lipase activity. Many of these derivatives had comparable or more potent activity than the clinically used lipase inhibitors such as orlistat. In addition, the lipase appears to be inhibited by a wide range of epoxyketone analogues regardless of the configuration of the epoxide in the epoxyketone moiety. The presented data in this study shows the first example of the use of epoxyketone peptides as novel lipase inhibitors.

Indexed as

PeptidesProteasome InhibitorsEnzyme InhibitorsEpoxy CompoundsHumansLipaseProteasome Endopeptidase ComplexEnzyme InhibitorsEpoxy CompoundsLipasePeptidesProteasome Endopeptidase ComplexProteasome Inhibitorsdyslipidemiaepoxyketonelipase inhibitorsnovel warheadobesitypeptide inhibitors

Identifiers

PMID35408660
PMCPMC9000415
OpenAlexW4221092345

What OpenQuestion 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 OpenQuestion graph.