Synthesis of N6-Substituted 3'-Ureidoadenosine Derivatives as Highly Potent Agonists at the Mutant A3 Adenosine Receptor

By Jeong Lak Shin   Choe Seung Ah   Kim Ae Yil   Kim Hea Ok   Gao Zhan-Guo   Jacobson Kenneth   Chun Moon Woo   Moon Hyung Ryong  

Nucleosides, Nucleotides & Nucleic Acids, Vol. 26, Iss. 6-7, 2007-06 ,pp. : 717-719

Taylor & Francis Ltd

Access to resources Recommend Favorite

Synthesis and biological evaluation of disubstituted N 6 -cyclopentyladenine analogues - the search for a neutral antagonist with high affinity for the adenosine A 1 receptor

By de Ligt R.A.F.   van der Klein P.A.M.   von Frijtag Drabbe Kunzel J.K.   Lorenzen A.   Ait El Maate F.   Fujikawa S.   van Westhoven R.   van den Hoven T.   Brussee J.   IJzerman A.P.  

Bioorganic and Medicinal Chemistry, Vol. 12, Iss. 1, 2004-01 ,pp. : 139-149

Elsevier

Access to resources Recommend Favorite

[ 3 H]-( R )- N 6 -Phenylisopropyladenosine Agonist Binding to the Solubilized A 1 Adenosine Receptor from Bovine Epidydimal Spermatozoa

By Minelli A.   Allegrucci C.   Mezzasoma I.  

Archives of Biochemistry and Biophysics, Vol. 337, Iss. 1, 1997-01 ,pp. : 54-61

Elsevier

Access to resources Recommend Favorite

6-Methyl-3′-bromoflavone, a High-Affinity Ligand for the Benzodiazepine Binding Site of the GABA_A Receptor with Some Antagonistic Properties

By Viola H.   Marder M.   Nuñez J.   Izquierdo L.   Wasowski C.   Wolfman C.   Ardenghi P.   Barros D.   Medina J.H.   Paladini A.C.  

Biochemical and Biophysical Research Communications, Vol. 262, Iss. 3, 1999-09 ,pp. : 643-646

Elsevier

Access to resources Recommend Favorite

Design, Synthesis, and Anti-Tumor Activity of 4'-Thionucleosides as Potent and Selective Agonists at the Human A3 Adenosine Receptor

By Jeong Lak Shin   Lee Hyuk Woo   Kim Hea Ok   Jung Ji Young   Gunaga Prashantha   Lee Sang Kook   Lee Eun-Jin   Chun Moon Woo   Gao Zhan-Guo   Jacobson Kenneth   Moon Hyung Ryong  

Nucleosides, Nucleotides & Nucleic Acids, Vol. 26, Iss. 10-12, 2007-10 ,pp. : 1565-1568

Taylor & Francis Ltd

Access to resources Recommend Favorite