35S GTP S autoradiography; Allosteric modulator; Cysteine; Dithiotreitol; G protein coupled receptor; Heterotrimeric G protein; SCH 202676; Sulphydryl; Thiadiazole; Thiol
SCH-202676: An allosteric modulator of both agonist and antagonist binding to G protein-coupled receptors
FAWZI, A.B., MACDONALD, D., BENBOW, L.L., SMITH-TORHAN, A., ZHANG, H., WEIG, B.C., HO, G., TULSHIAN, D., LINDER, M.E. & GRAZIANO, M.P. (2001). SCH-202676: an allosteric modulator of both agonist and antagonist binding to G protein-coupled receptors. Mol. Pharmacol., 59, 30-37.
Effects of the allosteric modulator SCH-202676 on adenosine and P2Y receptors
GAO, Z.G., GROSS, A.S. & JACOBSON, K.A. (2004). Effects of the allosteric modulator SCH-202676 on adenosine and P2Y receptors. Life Sci., 74, 3173-3180.
Synthesis and biological evaluation of a new series of 2,3,5-substituted [1,2,4]-thiadiazoles as modulators of adenosine A1 receptors and their molecular mechanism of action
GOBLYOS, A., DE VRIES, H., BRUSSEE, J. & IJZERMAN, A.P. (2005). Synthesis and biological evaluation of a new series of 2,3,5-substituted [1,2,4]-thiadiazoles as modulators of adenosine A1 receptors and their molecular mechanism of action. J. Med. Chem., 48, 1145-1151.
35S]GTP autoradiography allows region-specific detection of muscarinic receptor-dependent G protein activation in the chick optic tectum
35S]GTP autoradiography allows region-specific detection of muscarinic receptor-dependent G protein activation in the chick optic tectum. Brain Res., 769, 21-28.
32P]diphosphate. An agonist and radio-ligand for the receptor that inhibits the accumulation of cyclic AMP in intact blood platelets
32P]diphosphate. An agonist and radio-ligand for the receptor that inhibits the accumulation of cyclic AMP in intact blood platelets. J. Clin. Invest., 71, 420-428.
Synthesis and biological evaluation of 2,3,5-substituted [1,2,4]thiadiazoles as allosteric modulators of adenosine receptors
VAN DEN NIEUWENDIJK, A.M., PIETRA, D., HEITMAN, L., GOBLYOS, A. & IJZERMAN, A.P. (2004). Synthesis and biological evaluation of 2,3,5-substituted [1,2,4]thiadiazoles as allosteric modulators of adenosine receptors. J. Med. Chem., 47, 663-672.