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The discovery of a novel series of glucokinase activators based on a pyrazolopyrimidine scaffold.

Authors :
Bonn P
Brink DM
Fägerhag J
Jurva U
Robb GR
Schnecke V
Svensson Henriksson A
Waring MJ
Westerlund C
Source :
Bioorganic & medicinal chemistry letters [Bioorg Med Chem Lett] 2012 Dec 15; Vol. 22 (24), pp. 7302-5. Date of Electronic Publication: 2012 Oct 27.
Publication Year :
2012

Abstract

Glucokinase is a key enzyme in glucose homeostasis since it phosphorylates glucose to give glucose-6-phosphate, which is the first step in glycolysis. GK activators have been proven to lower blood-glucose, and therefore have potential as treatments for type 2 diabetes. Here the discovery of pyrazolopyrimidine GKAs is reported. An original singleton hit from a high-throughput screen with micromolar levels of potency was optimised to give compounds with nanomolar activities. Key steps in this success were the introduction of an extra side-chain, which increased potency, and changing the linking functionality from a thioether to an ether, which led to improved potency and lipophilic ligand efficiency. This also led to more stable compounds with improved profiles in biological assays.<br /> (Copyright © 2012 Elsevier Ltd. All rights reserved.)

Details

Language :
English
ISSN :
1464-3405
Volume :
22
Issue :
24
Database :
MEDLINE
Journal :
Bioorganic & medicinal chemistry letters
Publication Type :
Academic Journal
Accession number :
23149230
Full Text :
https://doi.org/10.1016/j.bmcl.2012.10.090