Please use this identifier to cite or link to this item: https://www.um.edu.mt/library/oar/handle/123456789/48756
Title: Drug design of de novo designed molecules at the peroxisome proliferator activated receptor
Authors: Portelli, Stephanie
Shoemake, Claire
Azzopardi, Lilian M.
Keywords: Drugs -- Design
Peroxisomes -- Receptors
Rosiglitazone
Diabetes -- Treatment
Issue Date: 2013-08
Publisher: University of Malta. Department of Pharmacy
Citation: Portelli, S., Shoemake, C., & Azzopardi, L. M. (2013, August). Drug design of de novo designed molecules at the peroxisome proliferator activated receptor. Poster session presented at the International Pharmaceutical Federation (FIP) World Congress, Dublin, Ireland.
Abstract: A poster presentation regarding drug design of de novo designed molecules at the peroxisome proliferator activated receptor. Introduction: Following rosiglitazone withdrawal, newer therapies aiming at the Peroxisome Proliferator Activated Receptor y (PPARγ) as treatment for type 2 diabetes acting mainly via partial agonism are being studied. Such partial agonists include selective PPARγ modulators such as S-26948. Aim: To obtain and optimise molecules having a high affinity to PPARγ, and which are also Lipinski Rule compliant.
URI: https://www.um.edu.mt/library/oar/handle/123456789/48756
Appears in Collections:Scholarly Works - FacM&SPha



Items in OAR@UM are protected by copyright, with all rights reserved, unless otherwise indicated.