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1N6-methoxy-2-alkynyladenosine derivatives as highly potent and selective ligands at the human A3 adenosine receptor
R. Volpini, D. Ben, C. Lambertucci, S. Taffi, S. Vittori, K. Klotz, and G. Cristalli. J Med Chem, 50 (6): 1222-30 (March 2007)Volpini, Rosaria Dal Ben, Diego Lambertucci, Catia Taffi, Sara Vittori, Sauro Klotz, Karl-Norbert Cristalli, Gloria Research Support, Non-U.S. Gov't United States Journal of medicinal chemistry J Med Chem. 2007 Mar 22;50(6):1222-30. Epub 2007 Feb 20..
14 years ago by @pharmawuerz
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derivatives/*chemical
Adenosine/*analogs
Cricetinae
&
Radioligand
A3/*agonists
Sequence
Animals
Receptor
Cyclic
Relationship
Ligands
*Models,
Structure-Activity
Adenosine
Rhodopsin/chemistry
Acid
Cricetulus
Humans
Proteins/agonists
CHO
Assay
Molecular
Homology,
AMP/biosynthesis
synthesis/chemistry/pharmacology
Amino
Recombinant
Alkynes/*chemical
Cell
derivatives/*chemicalAdenosine/*analogsCricetinae&RadioligandA3/*agonistsSequenceAnimalsReceptorCyclicRelationshipLigands*Models,Structure-ActivityAdenosineRhodopsin/chemistryAcidCricetulusHumansProteins/agonistsCHOAssayMolecularHomology,AMP/biosynthesissynthesis/chemistry/pharmacologyAminoRecombinantAlkynes/*chemicalCell
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