1351069-92-5Relevant articles and documents
Stereoselective synthesis of (RP)-8-substituted-N 6-acylated and N6-alkylated adenosine-3′,5′- cyclic phosphorothioic acids as cAMP antagonists
Andrei, Mioara,Bakkeb?, Tina,Klaveness, Jo,Taskén, Kjetil,Undheim, Kjell
, p. 5935 - 5940 (2011)
N6-Monoalkylated, N6-dialkylated and N 6-acylated (RP)-adenosine 3′,5′-cyclic phosphorothioic acids have been prepared by stereoselective syntheses from cAMP for a study of protein kinase A antagonist activity.