Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1366093 | Bioorganic & Medicinal Chemistry Letters | 2007 | 4 Pages |
Abstract
All-O-undec-en-10-yl derivatives of d-glucose have been prepared and their affinities for the Plasmodium falciparum hexose transporter (PfHT) determined; the O-2 derivative displays a good apparent affinity for PfHT (KI = 2 μM) with no significant interaction with the mammalian transporter GLUT1. This selectivity points to position â2 of glucose as an appropriate substitution site for the development of inhibitors of P. falciparum glucose uptake.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Marina Ionita, Sanjeev Krishna, Pierre-Marc Léo, Christophe Morin, Asha Parbhu Patel,