Volume 31, Issue 23
Heterocyclic Compounds
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ChemInform Abstract: Acyclic Analogues of Deoxyadenosine 3′,5′-Bisphosphates as P2Y1 Receptor Antagonists.

Yong-Chul Kim

Yong-Chul Kim

Mol. Recognit. Sect., NIH, Bethesda, MD 20892, USA

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Carola Gallo-Rodriguez

Carola Gallo-Rodriguez

Mol. Recognit. Sect., NIH, Bethesda, MD 20892, USA

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Soo-Yeon Jang

Soo-Yeon Jang

Mol. Recognit. Sect., NIH, Bethesda, MD 20892, USA

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Erathodiyil Nandanan

Erathodiyil Nandanan

Mol. Recognit. Sect., NIH, Bethesda, MD 20892, USA

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Mary Adams

Mary Adams

Mol. Recognit. Sect., NIH, Bethesda, MD 20892, USA

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T. Kendall Harden

T. Kendall Harden

Mol. Recognit. Sect., NIH, Bethesda, MD 20892, USA

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Jose L. Boyer

Jose L. Boyer

Mol. Recognit. Sect., NIH, Bethesda, MD 20892, USA

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Kenneth A. Jacobson

Kenneth A. Jacobson

Mol. Recognit. Sect., NIH, Bethesda, MD 20892, USA

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First published: 08 June 2010

Abstract

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ChemInform Abstract

Some new acyclic nucleotide analogues are synthesized as ligands for the P2Y1 receptor. Three groups of adenine derivatives (I), (II), and (III) which contain two symmetrical phosphate or phosphonate groups in place of the ribose moiety are prepared. Their biological activity is demonstrated by the ability to act as agonists or antagonists in the simulation of phospholipase C in turkey erythrocyte membranes. The highest affinity among the three novel structures exhibit the 2-chloro-N-methyl gancyclovir equivalent (Ib).

chemical structure image

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