Does the combination of optimal substitutions at the C 2-, N 5- and N 8-positions of the pyrazolo-triazolo-pyrimidine scaffold guarantee selective modulation of the human A 3 adenosine receptors?

10.1016/j.bmc.2011.08.026

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Main Authors: Cheong, S.L., Dolzhenko, A.V., Paoletta, S., Lee, E.P.R., Kachler, S., Federico, S., Klotz, K.-N., Spalluto, G., Moro, S., Pastorin, G.
Other Authors: PHARMACY
Format: Article
Published: 2014
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Online Access:http://scholarbank.nus.edu.sg/handle/10635/105850
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spelling sg-nus-scholar.10635-1058502023-10-26T21:48:40Z Does the combination of optimal substitutions at the C 2-, N 5- and N 8-positions of the pyrazolo-triazolo-pyrimidine scaffold guarantee selective modulation of the human A 3 adenosine receptors? Cheong, S.L. Dolzhenko, A.V. Paoletta, S. Lee, E.P.R. Kachler, S. Federico, S. Klotz, K.-N. Dolzhenko, A.V. Spalluto, G. Moro, S. Pastorin, G. PHARMACY 2-Phenyl-pyrazolo-triazolo-pyrimidines Affinity Human A 3 adenosine receptor antagonists Selectivity Structure-affinity relationship 10.1016/j.bmc.2011.08.026 Bioorganic and Medicinal Chemistry 19 20 6120-6134 BMECE 2014-10-29T01:51:35Z 2014-10-29T01:51:35Z 2011-10-15 Article Cheong, S.L., Dolzhenko, A.V., Paoletta, S., Lee, E.P.R., Kachler, S., Federico, S., Klotz, K.-N., Dolzhenko, A.V., Spalluto, G., Moro, S., Pastorin, G. (2011-10-15). Does the combination of optimal substitutions at the C 2-, N 5- and N 8-positions of the pyrazolo-triazolo-pyrimidine scaffold guarantee selective modulation of the human A 3 adenosine receptors?. Bioorganic and Medicinal Chemistry 19 (20) : 6120-6134. ScholarBank@NUS Repository. https://doi.org/10.1016/j.bmc.2011.08.026 09680896 http://scholarbank.nus.edu.sg/handle/10635/105850 000295494600021 Scopus
institution National University of Singapore
building NUS Library
continent Asia
country Singapore
Singapore
content_provider NUS Library
collection ScholarBank@NUS
topic 2-Phenyl-pyrazolo-triazolo-pyrimidines
Affinity
Human A 3 adenosine receptor antagonists
Selectivity
Structure-affinity relationship
spellingShingle 2-Phenyl-pyrazolo-triazolo-pyrimidines
Affinity
Human A 3 adenosine receptor antagonists
Selectivity
Structure-affinity relationship
Cheong, S.L.
Dolzhenko, A.V.
Paoletta, S.
Lee, E.P.R.
Kachler, S.
Federico, S.
Klotz, K.-N.
Dolzhenko, A.V.
Spalluto, G.
Moro, S.
Pastorin, G.
Does the combination of optimal substitutions at the C 2-, N 5- and N 8-positions of the pyrazolo-triazolo-pyrimidine scaffold guarantee selective modulation of the human A 3 adenosine receptors?
description 10.1016/j.bmc.2011.08.026
author2 PHARMACY
author_facet PHARMACY
Cheong, S.L.
Dolzhenko, A.V.
Paoletta, S.
Lee, E.P.R.
Kachler, S.
Federico, S.
Klotz, K.-N.
Dolzhenko, A.V.
Spalluto, G.
Moro, S.
Pastorin, G.
format Article
author Cheong, S.L.
Dolzhenko, A.V.
Paoletta, S.
Lee, E.P.R.
Kachler, S.
Federico, S.
Klotz, K.-N.
Dolzhenko, A.V.
Spalluto, G.
Moro, S.
Pastorin, G.
author_sort Cheong, S.L.
title Does the combination of optimal substitutions at the C 2-, N 5- and N 8-positions of the pyrazolo-triazolo-pyrimidine scaffold guarantee selective modulation of the human A 3 adenosine receptors?
title_short Does the combination of optimal substitutions at the C 2-, N 5- and N 8-positions of the pyrazolo-triazolo-pyrimidine scaffold guarantee selective modulation of the human A 3 adenosine receptors?
title_full Does the combination of optimal substitutions at the C 2-, N 5- and N 8-positions of the pyrazolo-triazolo-pyrimidine scaffold guarantee selective modulation of the human A 3 adenosine receptors?
title_fullStr Does the combination of optimal substitutions at the C 2-, N 5- and N 8-positions of the pyrazolo-triazolo-pyrimidine scaffold guarantee selective modulation of the human A 3 adenosine receptors?
title_full_unstemmed Does the combination of optimal substitutions at the C 2-, N 5- and N 8-positions of the pyrazolo-triazolo-pyrimidine scaffold guarantee selective modulation of the human A 3 adenosine receptors?
title_sort does the combination of optimal substitutions at the c 2-, n 5- and n 8-positions of the pyrazolo-triazolo-pyrimidine scaffold guarantee selective modulation of the human a 3 adenosine receptors?
publishDate 2014
url http://scholarbank.nus.edu.sg/handle/10635/105850
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