Evan E. Bolton; Yanli Wang; Paul A. Thiessen; Stephen H. Bryant (2008). „Chapter 12 PubChem: Integrated Platform of Small Molecules and Biological Activities”. Annual Reports in Computational Chemistry. 4: 217—241. doi:10.1016/S1574-1400(08)00012-1.
Zablocki JA, Wu L, Shryock J, Belardinelli L (2004). „Partial A(1) adenosine receptor agonists from a molecular perspective and their potential use as chronic ventricular rate control agents during atrial fibrillation (AF)”. Current Topics in Medicinal Chemistry. 4 (8): 839—54. PMID15078215. doi:10.2174/1568026043450998.
Hutchinson SA, Scammells PJ (2004). „A(1) adenosine receptor agonists: medicinal chemistry and therapeutic potential”. Current Pharmaceutical Design. 10 (17): 2021—39. PMID15279543. doi:10.2174/1381612043384204.
Elzein E, Kalla R, Li X, Perry T, Marquart T, Micklatcher M, Li Y, Wu Y, Zeng D, Zablocki J (2007). „N6-Cycloalkyl-2-substituted adenosine derivatives as selective, high affinity adenosine A1 receptor agonists”. Bioorganic & Medicinal Chemistry Letters. 17 (1): 161—6. PMID17045477. doi:10.1016/j.bmcl.2006.09.065.
Elzein E, Zablocki J (2008). „A1 adenosine receptor agonists and their potential therapeutic applications”. Expert Opinion on Investigational Drugs. 17 (12): 1901—10. PMID19012505. doi:10.1517/13543780802497284.
Franchetti P, Cappellacci L, Vita P, Petrelli R, Lavecchia A, Kachler S, Klotz KN, Marabese I, Luongo L, Maione S, Grifantini M (2009). „N6-Cycloalkyl- and N6-bicycloalkyl-C5'(C2')-modified adenosine derivatives as high-affinity and selective agonists at the human A1 adenosine receptor with antinociceptive effects in mice”. Journal of Medicinal Chemistry. 52 (8): 2393—406. PMID19317449. doi:10.1021/jm801456g.
Coffin VL, Spealman RD (1987). „Behavioral and cardiovascular effects of analogs of adenosine in cynomolgus monkeys”. The Journal of Pharmacology and Experimental Therapeutics. 241 (1): 76—83. PMID3572798.
Zablocki JA, Wu L, Shryock J, Belardinelli L (2004). „Partial A(1) adenosine receptor agonists from a molecular perspective and their potential use as chronic ventricular rate control agents during atrial fibrillation (AF)”. Current Topics in Medicinal Chemistry. 4 (8): 839—54. PMID15078215. doi:10.2174/1568026043450998.
Hutchinson SA, Scammells PJ (2004). „A(1) adenosine receptor agonists: medicinal chemistry and therapeutic potential”. Current Pharmaceutical Design. 10 (17): 2021—39. PMID15279543. doi:10.2174/1381612043384204.
Elzein E, Kalla R, Li X, Perry T, Marquart T, Micklatcher M, Li Y, Wu Y, Zeng D, Zablocki J (2007). „N6-Cycloalkyl-2-substituted adenosine derivatives as selective, high affinity adenosine A1 receptor agonists”. Bioorganic & Medicinal Chemistry Letters. 17 (1): 161—6. PMID17045477. doi:10.1016/j.bmcl.2006.09.065.
Elzein E, Zablocki J (2008). „A1 adenosine receptor agonists and their potential therapeutic applications”. Expert Opinion on Investigational Drugs. 17 (12): 1901—10. PMID19012505. doi:10.1517/13543780802497284.
Franchetti P, Cappellacci L, Vita P, Petrelli R, Lavecchia A, Kachler S, Klotz KN, Marabese I, Luongo L, Maione S, Grifantini M (2009). „N6-Cycloalkyl- and N6-bicycloalkyl-C5'(C2')-modified adenosine derivatives as high-affinity and selective agonists at the human A1 adenosine receptor with antinociceptive effects in mice”. Journal of Medicinal Chemistry. 52 (8): 2393—406. PMID19317449. doi:10.1021/jm801456g.
