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J. Med. Chem. 2009, 52, 3430
Additions and Corrections
2009, Volume 52
Palmarisa Franchetti, Loredana Cappellacci, Patrizia Vita, Riccardo Petrelli, Antonio Lavecchia, Sonja Kachler, Karl-Norbert Klotz, Ida Marabese, Livio Luongo, Sabatino Maione, and Mario Grifantini*: N6-Cycloalkyl- and N6Bicycloalkyl-C5′(C2′)-modified Adenosine Derivatives as HighAffinity and Selective Agonists at the Human A1 Adenosine Receptor with Antinociceptive Effects in Mice. Page 2397. For the rightmost chemical structure in Table 1, the inclusion of 21 and 22 in the listing is incorrect; those compounds should be 23 and 24, respectively. Also, footnote b of Table 1, “Displacement of [3H]NECA binding in CHO cells stably transfected with human recombinant A1 or A3 adenosine receptors” should be “Displacement of [3H]NECA or [3H]HEMADO in CHO cells stably transfected with human recombinant A2A and A3 adenosine receptors, respectively”. JM900498H 10.1021/jm900498h Published on Web 04/27/2009
