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
ANIMAL CELL;
ARTICLE;
BINDING AFFINITY;
CHO CELL;
CONTROLLED STUDY;
DRUG MECHANISM;
DRUG RECEPTOR BINDING;
DRUG SYNTHESIS;
HIGH PERFORMANCE LIQUID CHROMATOGRAPHY;
INHIBITION KINETICS;
LIGAND BINDING;
MASS SPECTROMETRY;
NONHUMAN;
Allosteric modulation of G protein-coupled receptors
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International Union of Pharmacology Committee on Receptor Nomenclature and Drug Classification. XXXVIII. Update on terms and symbols in quantitative pharmacology
Neubig, R. R.; Spedding, M.; Kenakin, T.; Christopoulos, A. International Union of Pharmacology Committee on Receptor Nomenclature and Drug Classification. XXXVIII. Update on Terms and Symbols in Quantitative Pharmacology. Pharmacol. Rev. 2003, 55, 597-606.
1 receptor. Synthesis and biological evaluation of novel 2-amino-3-benzoylthiophenes as allosteric enhancers of agonist binding
1 Receptor. Synthesis and Biological Evaluation of Novel 2-Amino-3-benzoylthiophenes as Allosteric Enhancers of Agonist Binding. J. Med. Chem. 1999, 42, 3629-3635.
SCH-202676: An allosteric modulator of both agonist and antagonist binding to G protein-coupled receptors
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Synthesis and biological evaluation of 2,3,5-substituted [1,2,4]thiadiazoles as allostric modulators of adenosine receptors
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Effects of the allosteric modulator SCH-202676 on adenosine and P2Y receptors
Gao, Z. G.; Gross, A. S.; Jacobson, K. A. Effects of the Allosteric Modulator SCH-202676 on Adenosine and P2Y Receptors. Life Sci. 2004, 74, 3173-3180.
Herstellung von (N-alkylbenzimidoyl)-und (N-arylbenzimidoyl) carbodiimiden; ihre umlagerung zu aminochinazolinen und dihydro-1,3,5-triazinen
(a) Goerdeler, J.; Eggers, W. Herstellung von (N-Alkylbenzimidoyl)-und (N-Arylbenzimidoyl)carbodiimiden; ihre Umlagerung zu Aminochinazolinen und Dihydro-1,3,5-triazinen. Chem. Ber. 1986, 119, 3737-3748.
Relationship between the occurrence of cysteine in proteins and the complexity of organisms
Miseta, A.; Csutora, P. Relationship Between the Occurrence of Cysteine in Proteins and the Complexity of Organisms. Mol. Biol. Evol. 2000, 17, 1232-1239.
2,3-Diaryl-5-anilino[1,2,4]thiadiazoles as melanocortin MC4 receptor agonists and their effects on feeding behaviour in rats
Pan, K.; Scott, M. K.; Lee, D. H. S.; Fitzpatrick, L. J.; Crooke, J. J.; Rivero, R. A.; Rosenthal, D. I.; Vaidya, A. H.; Zhao, B.; Reitz, A. B. 2,3-Diaryl-5-anilino[1,2,4]thiadiazoles as Melanocortin MC4 Receptor Agonists and Their Effects on Feeding Behaviour in Rats. Bioorg. Med. Chem. 2003, 11, 185-192.
Synthesis and evaluation of novel dipeptide-bound 1,2,4-thiadiazoles as irreversible inhibitors of guinea pig liver transglutaminase
Marrano, C.; de Macédo, P.; Gagnon, P.; Lapierre, D.; Gravel, C.; Keillor, J. W. Synthesis and Evaluation of Novel Dipeptide-Bound 1,2,4-Thiadiazoles as Irreversible Inhibitors of Guinea Pig Liver Transglutaminase. Bioorg. Med. Chem. 2001, 9, 3231-3241.
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Thiadiazole Compounds Useful as Proton Pump Inhibitors. U.S. Patent 5,677,302, Oct 14, 1997
Karimian, K.; Tam, T. F.; Desilets, D.; Lee, S.; Cappelletto, T.; Li, W. Thiadiazole Compounds Useful as Proton Pump Inhibitors. U.S. Patent 5,677,302, Oct 14, 1997.
Agonist and antagonist affinities for inhibitory adenosine receptors are reciprocally affected by 5′-guanylylimidodiphosphate or N-ethylmaleimide
Yeung, S. M. H.; Green, R. D. Agonist and Antagonist Affinities for Inhibitory Adenosine Receptors Are Reciprocally Affected by 5′- Guanylylimidodiphosphate or N-Ethylmaleimide. J. Biol. Chem. 1983, 258, 2334-2339.