-transparent.png){kind=logo}
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.
Related Publications
D Camp, and
Y Li, and
A McCluskey, and
R W Moni, and
R J Quinn
March 1998,
Bioorganic & medicinal chemistry letters,
D Camp, and
Y Li, and
A McCluskey, and
R W Moni, and
R J Quinn
May 2010,
Acta crystallographica. Section E, Structure reports online,
D Camp, and
Y Li, and
A McCluskey, and
R W Moni, and
R J Quinn
September 2006,
Bioorganic & medicinal chemistry letters,
D Camp, and
Y Li, and
A McCluskey, and
R W Moni, and
R J Quinn
January 2015,
European journal of medicinal chemistry,
D Camp, and
Y Li, and
A McCluskey, and
R W Moni, and
R J Quinn
June 2015,
European journal of medicinal chemistry,
D Camp, and
Y Li, and
A McCluskey, and
R W Moni, and
R J Quinn
August 2012,
Organic & biomolecular chemistry,
D Camp, and
Y Li, and
A McCluskey, and
R W Moni, and
R J Quinn
April 2009,
European journal of medicinal chemistry,
D Camp, and
Y Li, and
A McCluskey, and
R W Moni, and
R J Quinn
November 2009,
European journal of medicinal chemistry,
D Camp, and
Y Li, and
A McCluskey, and
R W Moni, and
R J Quinn
January 2011,
European journal of medicinal chemistry,
D Camp, and
Y Li, and
A McCluskey, and
R W Moni, and
R J Quinn
April 2012,
Bioorganic & medicinal chemistry,
