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
Affiliations
Jehad Almaliti
Department Pharmaceutical Sciences, College of Pharmacy, The University of Jordan, Amman 11942, Jordan
Muhammed Alzweiri
Department Pharmaceutical Sciences, College of Pharmacy, The University of Jordan, Amman 11942, Jordan
Momen Alhindy
Department Pharmaceutical Sciences, College of Pharmacy, The University of Jordan, Amman 11942, Jordan
Tamam Al-Helo
Department Pharmaceutical Sciences, College of Pharmacy, The University of Jordan, Amman 11942, Jordan
Ibrahim Daoud
Department Pharmaceutical Sciences, College of Pharmacy, The University of Jordan, Amman 11942, Jordan
Raghad Deknash
Department Pharmaceutical Sciences, College of Pharmacy, The University of Jordan, Amman 11942, Jordan
C. Benjamin Naman
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
Hamdi Mango Center for Scientific Research, The University of Jordan, Amman 11942, Jordan
Yasser Bustanji
Department Pharmaceutical Sciences, College of Pharmacy, The University of Jordan, Amman 11942, Jordan
Islam Hamad
Department of Pharmacy, Faculty of Health Sciences, American University of Madaba, Madaba 11821, Jordan
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.