Search results for "Receptor"
showing 10 items of 6990 documents
Thermodynamics of sulfate anion binding by macrocyclic polyammonium receptors
2001
The interaction of SO42− with polyammonium cations derived from fourteen polyamines (5 polyazacycloalkanes, 2 polyazacyclophanes, 3 phenanthrolinacyclophanes, 2 dibenzenacyclophanes and 2 acyclic polyamines) in aqueous solution has been studied by means of potentiometric and microcalorimetric techniques. Only 1 : 1 receptor–anion complexes have been found in solution. Complexed species of considerable stability are formed, although the two acyclic polyamines (dimethylpentaethylenehexaamine and dimethylhexaethyleneheptaamine) and the smallest phenanthrolinacyclophane do not interact with the anion. The complexation reactions are endothermic, or almost athermic, and promoted by invariably fav…
Specific and Nonspecific Regulation of GPCR Function by Cholesterol
2012
Post-Translational Regulation of Fas/CD95 in Cell Death and Survival: Role of Nitric Oxide
2010
Icatibant, a Selective Bradykinin B2 Receptor Antagonist Used in Hereditary Angioedema Due to C1 Inhibitor Deficiency
2010
Acetylcholine receptors (muscarinic) (version 2019.4) in the IUPHAR/BPS Guide to Pharmacology Database
2019
Muscarinic acetylcholine receptors (nomenclature as agreed by the NC-IUPHAR Subcommittee on Muscarinic Acetylcholine Receptors [45]) are GPCRs of the Class A, rhodopsin-like family where the endogenous agonist is acetylcholine. In addition to the agents listed in the table, AC-42, its structural analogues AC-260584 and 77-LH-28-1, N-desmethylclozapine, TBPB and LuAE51090 have been described as functionally selective agonists of the M1 receptor subtype via binding in a mode distinct from that utilized by non-selective agonists [243, 242, 253, 155, 154, 181, 137, 11, 230]. There are two pharmacologically characterised allosteric sites on muscarinic receptors, one defined by it binding gallami…
Hg2+ and Cu2+ selective detection using a dual channel receptor based on thiopyrylium scaffoldings
2009
2,4,6-Triphenylthiopyrylium functionalized with an aza-oxa-thia macrocycle is able to selectively recognize Hg2+ cation by a color change and Cu2+ cation by a remarkable significant emission enhancement.
ChemInform Abstract: Synthesis and Muscarinic Activity of Isoxazole-Substituted 1,2,5,6- Tetrahydropyridines.
2010
ChemInform Abstract: Design and Pharmacology of Quinuclidine Derivatives as M2-Selective Muscarinic Receptor Ligands.
2010
Novel Porphyrin-cholic Acid Conjugates as Receptors for Biologically Important Anions
2007
Anion Receptors Based on a Quinoline Backbone
2007
2-Amido-8-urea substituted quinoline derivatives are potent receptors for the binding of halide or benzoate anions in chloroform. The selectivity and affinity of the receptors for fluoride can be tuned by variation of the substituents at the receptor side chains. Computational considerations show that the cleft of the receptors provides space for effective binding of F–, but not bigger anions.(© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007)