Pyrazolo4,3-e-1,2,4-triazolo1,5-cpyrimidine derivatives as highly
potent and selective human A(3) adenosine receptor antagonists
P. Baraldi, B. Cacciari, R. Romagnoli, G. Spalluto, K. Klotz, E. Leung, K. Varani, S. Gessi, S. Merighi, and P. Borea. J Med Chem, 42 (22):
4473-8(November 1999)Baraldi, P G Cacciari, B Romagnoli, R Spalluto, G Klotz, K N Leung,
E Varani, K Gessi, S Merighi, S Borea, P A In Vitro Research Support,
Non-U.S. Gov't United states Journal of medicinal chemistry J Med
Chem. 1999 Nov 4;42(22):4473-8..
Baraldi, P G Cacciari, B Romagnoli, R Spalluto, G Klotz, K N Leung,
E Varani, K Gessi, S Merighi, S Borea, P A In Vitro Research Support,
Non-U.S. Gov't United states Journal of medicinal chemistry J Med
Chem. 1999 Nov 4;42(22):4473-8.
Please log in to take part in the discussion (add own reviews or comments).
Cite this publication
More citation styles
- please select -
%0 Journal Article
%1 Baraldi1999
%A Baraldi, P. G.
%A Cacciari, B.
%A Romagnoli, R.
%A Spalluto, G.
%A Klotz, K. N.
%A Leung, E.
%A Varani, K.
%A Gessi, S.
%A Merighi, S.
%A Borea, P. A.
%D 1999
%J J Med Chem
%K AMP/biosynthesis Adenosine Animals Binding, Brain/metabolism CHO Competitive Cricetinae Cyclic Humans P1/*antagonists Purinergic Pyrazoles/*chemical Pyrimidines/*chemical Rats Relationship Structure-Activity inhibitors/metabolism synthesis/chemistry/metabolism/pharmacology Receptor Cell
%N 22
%P 4473-8
%T Pyrazolo4,3-e-1,2,4-triazolo1,5-cpyrimidine derivatives as highly
potent and selective human A(3) adenosine receptor antagonists
%U http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=10579811
%V 42
@article{Baraldi1999,
added-at = {2010-12-14T18:12:02.000+0100},
author = {Baraldi, P. G. and Cacciari, B. and Romagnoli, R. and Spalluto, G. and Klotz, K. N. and Leung, E. and Varani, K. and Gessi, S. and Merighi, S. and Borea, P. A.},
biburl = {https://www.bibsonomy.org/bibtex/20c6e609ab6c60cb24457a37d75828fd4/pharmawuerz},
endnotereftype = {Journal Article},
interhash = {803e5acb73f9408662f3003a21fbd498},
intrahash = {0c6e609ab6c60cb24457a37d75828fd4},
issn = {0022-2623 (Print) 0022-2623 (Linking)},
journal = {J Med Chem},
keywords = {AMP/biosynthesis Adenosine Animals Binding, Brain/metabolism CHO Competitive Cricetinae Cyclic Humans P1/*antagonists Purinergic Pyrazoles/*chemical Pyrimidines/*chemical Rats Relationship Structure-Activity inhibitors/metabolism synthesis/chemistry/metabolism/pharmacology Receptor Cell},
month = {Nov 4},
note = {Baraldi, P G Cacciari, B Romagnoli, R Spalluto, G Klotz, K N Leung,
E Varani, K Gessi, S Merighi, S Borea, P A In Vitro Research Support,
Non-U.S. Gov't United states Journal of medicinal chemistry J Med
Chem. 1999 Nov 4;42(22):4473-8.},
number = 22,
pages = {4473-8},
shorttitle = {Pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidine derivatives as highly
potent and selective human A(3) adenosine receptor antagonists},
timestamp = {2010-12-14T18:20:38.000+0100},
title = {Pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidine derivatives as highly
potent and selective human A(3) adenosine receptor antagonists},
url = {http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=10579811},
volume = 42,
year = 1999
}