Results 1 - 7 of 7 (Click here to explore results)

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

Edaravone containing isoindoline nitroxides for the potential treatment of cardiovascular ischaemia. James R. Walker, Kathryn E. Fairfull-Smith, Kazunori Anzai, Shannen Lau, Paul J. White, Peter J. Scammells, Steven E. Bottle , Med. Chem. Commun. , 2011 , 2 , 436

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

Tricyclic xanthine derivatives containing a basic substituent: adenosine receptor affinity and drug-related properties. Michał Załuski, Katarzyna Stanuch, Tadeusz Karcz, Sonja Hinz, Gniewomir Latacz, Ewa Szymańska, Jakub Schabikowski, Agata Doroż-Płonka, Jadwiga Handzlik, Anna Drabczyńska, Christa E. Müller, Katarzyna Kieć-Kononowicz , Med. Chem. Commun. , 2018 , 9 , 951

Expeditious synthesis and biological evaluation of new C-6 1,2,3-triazole adenosine derivatives A1 receptor antagonists or agonists. Smitha C. Mathew, Youlet By, Aurélie Berthault, Marie-Alice Virolleaud, Louis Carrega, Gaëlle Chouraqui, Laurent Commeiras, Jocelyne Condo, Mireille Attolini, Anouk Gaudel-Siri, Jean Ruf, Jean Rodriguez, Jean-Luc Parrain, Régis Guieu , Org. Biomol. Chem. , 2010 , 8 , 3874

Methoxy substituted 2-benzylidene-1-indanone derivatives as A1 and/or A2A AR antagonists for the potential treatment of neurological conditions. Helena D. Janse van Rensburg, Lesetja J. Legoabe, Gisella Terre'Blanche, Mietha M. Van der Walt , Med. Chem. Commun. , 2019 , 10 , 300

Solid phase synthesis of C2,N ⁶-disubstituted adenosine analogues. Boris Rodenko, Martin J. Wanner, Gerrit-Jan Koomen , J. Chem. Soc., Perkin Trans. 1 , 2002 , 1247