Synthesis and biological evaluation of allosteric A1-adenosine receptor modulators structurally related to (2-amino-4,5,6,7-tetrahydro-benzo[b] thiophen-3-yl)-(4-chloro-phenyl)-methanone, a potent compound useful to reduce neuropathic pain
ALLOSTERISM;
ANIMAL TISSUE;
ARTICLE;
CELL ASSAY;
CHO CELL;
CONCENTRATION RESPONSE;
CONTROLLED STUDY;
DRUG BINDING;
DRUG MECHANISM;
DRUG SCREENING;
DRUG STRUCTURE;
DRUG SYNTHESIS;
HUMAN;
HUMAN CELL;
HUMAN TISSUE;
MALE;
NONHUMAN;
RAT;
International Union of Pharmacology. XXV. Nomenclature and classification of adenosine receptors
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Adenosine receptors subtypes: New insights from cloning and functional studies
Jacobson, K.A., Jarvis, M.F. (Eds.), Wiley-Liss, New York
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Allosteric enhancement of adenosine A1 receptor binding and function by 2-amino-3-benzoylthiophenes
Bruns, R.F., Fergus, J.H. Allosteric enhancement of adenosine A1 receptor binding and function by 2-amino-3-benzoylthiophenes. Mol. Pharmacol. 1990, 38, 939-948.
Synthesis and antiparasitic activity of 2,4-diamino-6-(arylmethyl)-5,6,7, 8-tetrahydroquinazoline analogues of Piritrexim
Rosowsky, A., Papoulis, A.T., Forsch, R.A., Qeener, S.F. Synthesis and antiparasitic activity of 2,4-diamino-6-(arylmethyl)-5,6,7,8- tetrahydroquinazoline analogues of Piritrexim. J. Med. Chem., 1999, 42, 1007-1017.
Thiaaromatics. VII. 1,2-Dithiolium salt from 1,3-dithiacyclohexenes by dehydrogenation with ring contraction
Luettringhaus, A., Mohr, M., Engelhard, N. Thiaaromatics. VII. 1,2-Dithiolium salt from 1,3-dithiacyclohexenes by dehydrogenation with ring contraction. Justus Liebigs Ann. Chem. 1963, 661, 84-94.
Bicyclo[3.1.0]hexane derivatives. I. Synthesis of bicyclo[3.1.0]-2- hexanone and methyl bicyclo[3.1.0]hexane-1-carboxylate
Nelson, N. A., Mortimer, G. A. Bicyclo[3.1.0]hexane derivatives. I. Synthesis of bicyclo[3.1.0]-2-hexanone and methyl bicyclo[3.1.0]hexane-1- carboxylate. J. Org. Chem. 1957, 22, 1146-1153.
4-Substituted cyclohexanones. Predicting the facial selectivity of nucleophilic attacks from the geometrical changes on cation-carbonyl complexation: An ab initio investigation
Yadav, V. K., Jeyaraj, D. A. 4-Substituted cyclohexanones. predicting the facial selectivity of nucleophilic attacks from the geometrical changes on cation-carbonyl complexation: An ab initio investigation. J. Org. Chem. 1998, 63, 3474-3477.
Heterocycles from CH-acidic nitriles. VIII. 2-Aminothiophenes from methylene-active nitriles, carbonyl compounds and sulfur
Gewald, K., Schinke, E., Böettcher, H. Heterocycles from CH-acidic nitriles. VIII. 2-Aminothiophenes from methylene-active nitriles, carbonyl compounds and sulfur. Chem. Ber., 1966, 99, 94-100.
Synthesis and biological effects of a new series of 2-amino-3- benzoylthiophenes as allosteric enhancers of A1-adenosine receptor
Baraldi, P.G., Zaid, A.N., Lampronti, I., Fruttarolo, F., Pavani, M.G., Tabrizi, M.A., Shryock, J.C., Leung, E., Romagnoli, R. Synthesis and biological effects of a new series of 2-amino-3-benzoylthiophenes as allosteric enhancers of A1-adenosine receptor. Bioorg. Med. Chem. Lett. 2000, 10, 1953-1957.
Inverse agonists and neutral antagonists of recombinant human A1 adenosine receptors stably expressed in Chinese hamster ovary cells
Shryock, J.C., Ozeck, M.J., Belardinelli, L. Inverse agonists and neutral antagonists of recombinant human A1 adenosine receptors stably expressed in Chinese hamster ovary cells. Mol. Pharmacol. 1998, 53, 886-893.
A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding
Bradford, M.M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal. Biochem. 1976, 72, 72:248-54.