N6-Cycloalkyl- and N6-Bicycloalkyl-C5′(C2′)-modified Adenosine Derivatives as High-Affinity and Selective Agonists at the Human A1 Adenosine Receptor …
P Franchetti, L Cappellacci, P Vita… - Journal of medicinal …, 2009 - ACS Publications
To further investigate new potent and selective human A1 adenosine receptor agonists, we
have synthesized a series of 5′-chloro-5′-deoxy-and 5′-(2-fluorophenylthio)-5′-deoxy …
have synthesized a series of 5′-chloro-5′-deoxy-and 5′-(2-fluorophenylthio)-5′-deoxy …
N6-Cycloalkyl-and N6-Bicycloalkyl-C5′(C2′)-modified Adenosine Derivatives as High-Affinity and Selective Agonists at the Human A (1) Adenosine Receptor with …
P Franchetti, L Cappellacci, P Vita… - JOURNAL OF …, 2009 - pubblicazioni.unicam.it
To further investigate new potent and selective human A (1) adenosine receptor agonists,
we have synthesized a series of 5'-chloro-5'-deoxy-and 5'-(2-fluorophenylthio)-5'-deoxy-N-6 …
we have synthesized a series of 5'-chloro-5'-deoxy-and 5'-(2-fluorophenylthio)-5'-deoxy-N-6 …
N6-Cycloalkyl-and N6-Bicycloalkyl-C5'(C2')-modified adenosine derivatives as high-affinity and selective agonists at the human A1 adenosine receptor with …
P Franchetti, L Cappellacci, P Vita, R Petrelli… - JOURNAL OF …, 2009 - iris.unina.it
To further investigate new potent and selective human A (1) adenosine receptor agonists,
we have synthesized a series of 5'-chloro-5'-deoxy-and 5'-(2-fluorophenylthio)-5'-deoxy-N …
we have synthesized a series of 5'-chloro-5'-deoxy-and 5'-(2-fluorophenylthio)-5'-deoxy-N …
[引用][C] N 6-Cycloalkyl-and N 6-Bicycloalkyl-C 5′(C 2′)-modified Adenosine Derivatives as High-Affinity and Selective Agonists at the Human A 1 Adenosine …
P Franchetti, L Cappellacci, P Vita, R Petrelli… - Journal of Medicinal …, 2009 - infona.pl
N 6 -Cycloalkyl- and N 6 -Bicycloalkyl- C 5′( C 2′)-modified Adenosine Derivatives as
High-Affinity and Selective Agonists at the Human A 1 Adenosine Receptor with Antinociceptive …
High-Affinity and Selective Agonists at the Human A 1 Adenosine Receptor with Antinociceptive …
N6-Cycloalkyl- and N6-Bicycloalkyl-C5′(C2′)-modified Adenosine Derivatives as High-Affinity and Selective Agonists at the Human A1 Adenosine Receptor …
P Franchetti, L Cappellacci, P Vita… - Journal of Medicinal …, 2009 - ACS Publications
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 …
listing is incorrect; those compounds should be 23 and 24, respectively. Also, footnote b of …
N6-Cycloalkyl-and N6-bicycloalkyl-C5'(C2')-modified adenosine derivatives as high-affinity and selective agonists at the human A1 adenosine receptor with …
P Franchetti, L Cappellacci, P Vita… - Journal of Medicinal …, 2009 - europepmc.org
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 …
and selective agonists at the human A1 adenosine receptor with antinociceptive effects in …
N6-cycloalkyl-And n6-bicycloalkyl-c5'(c 2')-modified adenosine derivatives as high-affinity and selective agonists at the human A1 adenosine receptor with …
P Franchetti, L Cappellacci, P Vita… - JOURNAL OF …, 2009 - iris.unicampania.it
To further investigate new potent and selective human A1 adenosine receptor agonists, we
have synthesized a series of 5'-chloro-5'-deoxy-and 5'-(2-fluorophenylthio)-5'-deoxy-N6 …
have synthesized a series of 5'-chloro-5'-deoxy-and 5'-(2-fluorophenylthio)-5'-deoxy-N6 …
[引用][C] N6-Cycloalkyl-and N6-Bicycloalkyl-C5'(C2')-modified Adenosine Derivatives as High-Affinity and Selective Agonists at the Human A1 Adenosine Receptor with …
P FRANCHETTI, L CAPPELLACCI… - Journal of medicinal …, 2009 - pascal-francis.inist.fr
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 …
and Selective Agonists at the Human A1 Adenosine Receptor with Antinociceptive Effects in …
N6-Cycloalkyl-and N6-bicycloalkyl-C5'(C2')-modified adenosine derivatives as high-affinity and selective agonists at the human A1 adenosine receptor with …
P Franchetti, L Cappellacci, P Vita, R Petrelli… - Journal of Medicinal …, 2009 - hero.epa.gov
To further investigate new potent and selective human A (1) adenosine receptor agonists,
we have synthesized a series of 5'-chloro-5'-deoxy-and 5'-(2-fluorophenylthio)-5'-deoxy-N …
we have synthesized a series of 5'-chloro-5'-deoxy-and 5'-(2-fluorophenylthio)-5'-deoxy-N …
N6-Cycloalkyl-and N6-bicycloalkyl-C5'(C2')-modified adenosine derivatives as high-affinity and selective agonists at the human A1 adenosine receptor with …
P Franchetti, L Cappellacci, P Vita… - Journal of …, 2009 - pubmed.ncbi.nlm.nih.gov
To further investigate new potent and selective human A (1) adenosine receptor agonists,
we have synthesized a series of 5'-chloro-5'-deoxy-and 5'-(2-fluorophenylthio)-5'-deoxy-N …
we have synthesized a series of 5'-chloro-5'-deoxy-and 5'-(2-fluorophenylthio)-5'-deoxy-N …