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Bioorg Med Chem Lett ; 17(21): 6013-8, 2007 Nov 01.
Article in English | MEDLINE | ID: mdl-17827008

ABSTRACT

Starting from adenosine triphosphate (ATP), the identification of a novel series of P2Y(12) receptor antagonists and exploitation of their SAR is described. Modifications of the acidic side chain and the purine core and investigation of hydrophobic substituents led to a series of neutral molecules. The leading compound, 17 (AZD6140), is currently in a large phase III clinical trial for the treatment of acute coronary syndromes and prevention of thromboembolic clinical sequelae.


Subject(s)
Adenosine Triphosphate/therapeutic use , Adenosine/analogs & derivatives , Membrane Proteins/antagonists & inhibitors , Purinergic P2 Receptor Antagonists , Thrombosis/prevention & control , Adenosine/therapeutic use , Administration, Oral , Animals , Humans , Receptors, Purinergic P2Y12 , Ticagrelor
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