Title of article :
Diimidazo[1,2-c:4′,5′-e]pyrimidines: N6-N1 conformationally restricted adenosines
Author/Authors :
David Camp، نويسنده , , Ying Li، نويسنده , , Adam McCluskey، نويسنده , , Roger W. Moni، نويسنده , , Ronald J. Quinn، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 1998
Pages :
4
From page :
695
To page :
698
Abstract :
Tethering the N6-substituents of N6-substituted adenosines to N1 has resulted in a series of conformationally restricted adenosine analogues. The resultant diimidazo[1,2-c:4′,5′-e]pyrimidines were shown to be adenosine A1 selective.
Journal title :
Bioorganic & Medicinal Chemistry Letters
Serial Year :
1998
Journal title :
Bioorganic & Medicinal Chemistry Letters
Record number :
789306
Link To Document :
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