Bioorganic and Medicinal Chemistry Letters p. 695 - 698 (1998)
Update date:2022-08-29
Topics:
Camp, David
Li, Ying
McCluskey, Adam
Moni, Roger W.
Quinn, Ronald J.
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.
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