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- Design, synthesis and evaluation of N
6-substituted 2-aminoadenosine-5′-N-methylcarboxamides as A3 adenosine receptor agonists. Shane M. Devine, Lauren T. May, Peter J. Scammells
, Med. Chem. Commun.
, 2014
, 5
, 192
- Expanding the repertoire of methanocarba nucleosides from purinergic signaling to diverse targets. Kenneth A. Jacobson, Veronica Salmaso, R. Rama Suresh, Dilip K. Tosh
, RSC Med. Chem.
, 2021
, 12
, 1808
- Discovery of the first A1 adenosine receptor ligand based on the chromone scaffold. F. Cagide, J. Reis, A. Gaspar, D. Chavarria, S. Kachler, K. N. Klotz, L. R. Gomes, J. N. Low, S. Vilar, G. Hripcsak, F. Borges
, RSC Adv.
, 2016
, 6
, 46972
- New substituted 9-propyladenine derivatives as A2A
adenosine receptor antagonists. C. Lambertucci, M. Buccioni, D. Dal Ben, S. Kachler, G. Marucci, A. Spinaci, A. Thomas, K.-N. Klotz, R. Volpini
, Med. Chem. Commun.
, 2015
, 6
, 963
- Stabilised G protein-coupled receptors in structure-based drug design: a case study with adenosine A2A receptor. Stephen P. Andrews, Benjamin Tehan
, Med. Chem. Commun.
, 2013
, 4
, 52