Discovery of Novel Epoxyketone Peptides as Lipase Inhibitors.


Journal

Molecules (Basel, Switzerland)
ISSN: 1420-3049
Titre abrégé: Molecules
Pays: Switzerland
ID NLM: 100964009

Informations de publication

Date de publication:
31 Mar 2022
Historique:
received: 24 01 2022
revised: 21 03 2022
accepted: 26 03 2022
entrez: 12 4 2022
pubmed: 13 4 2022
medline: 14 4 2022
Statut: epublish

Résumé

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.

Identifiants

pubmed: 35408660
pii: molecules27072261
doi: 10.3390/molecules27072261
pmc: PMC9000415
pii:
doi:

Substances chimiques

Enzyme Inhibitors 0
Epoxy Compounds 0
Peptides 0
Proteasome Inhibitors 0
Lipase EC 3.1.1.3
Proteasome Endopeptidase Complex EC 3.4.25.1

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : the university of Jordan
ID : 2021-66/2020
Organisme : King Abdullah II Fund For Development (KAFD)
ID : 2020/10

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Auteurs

Jehad Almaliti (J)

Department Pharmaceutical Sciences, College of Pharmacy, The University of Jordan, Amman 11942, Jordan.
Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California San Diego, La Jolla, San Diego, CA 92093, USA.

Muhammed Alzweiri (M)

Department Pharmaceutical Sciences, College of Pharmacy, The University of Jordan, Amman 11942, Jordan.

Momen Alhindy (M)

Department Pharmaceutical Sciences, College of Pharmacy, The University of Jordan, Amman 11942, Jordan.

Tamam Al-Helo (T)

Department Pharmaceutical Sciences, College of Pharmacy, The University of Jordan, Amman 11942, Jordan.

Ibrahim Daoud (I)

Department Pharmaceutical Sciences, College of Pharmacy, The University of Jordan, Amman 11942, Jordan.

Raghad Deknash (R)

Department Pharmaceutical Sciences, College of Pharmacy, The University of Jordan, Amman 11942, Jordan.

C Benjamin Naman (CB)

Li 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.

Bashaer Abu-Irmaileh (B)

Hamdi Mango Center for Scientific Research, The University of Jordan, Amman 11942, Jordan.

Yasser Bustanji (Y)

Department Pharmaceutical Sciences, College of Pharmacy, The University of Jordan, Amman 11942, Jordan.
Department of Basic Medical Sciences, College of Medicine, University of Sharjah, Sharjah P.O. Box 27272, United Arab Emirates.

Islam Hamad (I)

Department of Pharmacy, Faculty of Health Sciences, American University of Madaba, Madaba 11821, Jordan.

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Classifications MeSH