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Synthesis and Study of 5′-Ester Prodrugs of N6-Cyclopentyladenosine, a Selective A1 Receptor Agonist

✍ Scribed by Alessandro Dalpiaz; Angelo Scatturin; Enea Menegatti; Fabrizio Bortolotti; Barbara Pavan; Carla Biondi; Elisa Durini; Stefano Manfredini


Book ID
110296667
Publisher
Springer US
Year
2001
Tongue
English
Weight
166 KB
Volume
18
Category
Article
ISSN
0724-8741

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Adenosine receptor prodrugs: Synthesis a
✍ Michel C. Maillard; Olga Nikodijević; Kathryn F. Lanoue; Deborah Berkich; Xiao-D 📂 Article 📅 1994 🏛 John Wiley and Sons 🌐 English ⚖ 977 KB

5'-Ester derivatives of the potent adenosine agonists N6-[4-[[[[4-[[[(2-acetylaminoethyl)amino]carbonyl]methyl] anilino]carbonyl]methyl]phenyl]adenosine (N-AcADAC; 1) and N6-cyclopentyladenosine (CPA; 2) were prepared as prodrugs. Both alkyl esters or carbonates (designed to enter the brain by virtu