کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1365554 | 981564 | 2007 | 6 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
From ATP to AZD6140: The discovery of an orally active reversible P2Y12 receptor antagonist for the prevention of thrombosis
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موضوعات مرتبط
مهندسی و علوم پایه
شیمی
شیمی آلی
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چکیده انگلیسی
Starting from adenosine triphosphate (ATP), the identification of a novel series of P2Y12 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.
Starting with ATP, the identification of novel P2Y12 receptor antagonists are described. The leading compound, 17 (AZD6140), is currently in a phase III clinical trial for the treatment of acute coronary syndromes.Figure optionsDownload as PowerPoint slide
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Bioorganic & Medicinal Chemistry Letters - Volume 17, Issue 21, 1 November 2007, Pages 6013–6018
Journal: Bioorganic & Medicinal Chemistry Letters - Volume 17, Issue 21, 1 November 2007, Pages 6013–6018
نویسندگان
Brian Springthorpe, Andrew Bailey, Patrick Barton, Timothy N. Birkinshaw, Roger V. Bonnert, Roger C. Brown, David Chapman, John Dixon, Simon D. Guile, Robert G. Humphries, Simon F. Hunt, Francis Ince, Anthony H. Ingall, Ian P. Kirk, Paul D. Leeson,