Identification of the A2 adenosine receptor binding subunit by photoaffinity crosslinking. - Wikidata - wikimedia - TriplyDB

Identification of the A2 adenosine receptor binding subunit by photoaffinity crosslinking.

Identification of the A2 adenosine receptor binding subunit by photoaffinity crosslinking.

http://www.wikidata.org/entity/Q34300432

about

Site-directed mutagenesis identifies residues involved in ligand recognition in the human A2a adenosine receptor 125I-4-(2-[7-amino-2-[2-furyl][1,2,4]triazolo[2,3-a][1,3,5] triazin-5-yl-amino]ethyl)phenol, a high affinity antagonist radioligand selective for the A2a adenosine receptor Hydrophilic side chains in the third and seventh transmembrane helical domains of human A2A adenosine receptors are required for ligand recognition Evaluation of homology modeling of G-protein-coupled receptors in light of the A(2A) adenosine receptor crystallographic structure.Molecular probes for muscarinic receptors: functionalized congeners of selective muscarinic antagonists Adenosine and ischemic preconditioning.Functionalized congener approach to the design of ligands for G protein-coupled receptors (GPCRs).Adenosine modulation of neurotransmission in penile erection.Agonist derived molecular probes for A2 adenosine receptors Adenosine A1 and A2 receptors: structure--function relationships A2A adenosine receptors from rat striatum and rat pheochromocytoma PC12 cells: characterization with radioligand binding and by activation of adenylate cyclase.8-(3-Isothiocyanatostyryl)caffeine Is a Selective, Irreversible Inhibitor of Striatal A(2)-Adenosine Receptors Characterization of human striatal A2-adenosine receptors using radioligand binding and photoaffinity labeling Chemical modification and irreversible inhibition of striatal A2a adenosine receptors.Mutagenesis reveals structure-activity parallels between human A2A adenosine receptors and biogenic amine G protein-coupled receptors.Glycoprotein nature of the A2-adenosine receptor binding subunit The A2 adenosine receptor: guanine nucleotide modulation of agonist binding is enhanced by proteolysis.Characterization of the locomotor depression produced by an A2-selective adenosine agonist.Adenosine receptors: pharmacology, structure-activity relationships, and therapeutic potential.[(3)H]XAC (xanthine amine congener) is a radioligand for A(2)-adenosine receptors in rabbit striatum.Solubilized rabbit striatal A2a-adenosine receptors: stability and antagonist binding Neurobiological applications of small molecule screening.Purine nucleosides and nucleotides as central nervous system modulators. Adenosine as the prototypic paracrine neuroactive substance.Biochemical properties of a P2Y-purinergic receptor.Affinity purification in target identification: the specificity challenge.Elucidating the role of the A2A adenosine receptor in neurodegeneration using neurons derived from Huntington's disease iPSCs.Functionalized congeners of tyrosine-based P2X(7) receptor antagonists: probing multiple sites for linking and dimerization.The orphan receptor cDNA RDC7 encodes an A1 adenosine receptor.Immunological identification of A2 adenosine receptors by two antipeptide antibody preparations.Distinct pathways of desensitization of A1- and A2-adenosine receptors in DDT1 MF-2 cells.Demonstration of both A1 and A2 adenosine receptors in DDT1 MF-2 smooth muscle cells A covalent antagonist for the human adenosine A2A receptor.Structure-activity relationships of 8-styrylxanthines as A2-selective adenosine antagonists.Solubilization and characterization of the A2-adenosine receptor.

P2860

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P2860

Identification of the A2 adenosine receptor binding subunit by photoaffinity crosslinking.

http://www.wikidata.org/entity/Q34300432

description

1989 nî lūn-bûn

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1989 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

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1989 թվականի սեպտեմբերին հրատարակված գիտական հոդված

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1989年の論文

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1989年論文

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1989年論文

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1989年論文

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1989年論文

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1989年論文

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1989年论文

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name

Identification of the A2 adeno ...... by photoaffinity crosslinking.

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Identification of the A2 adeno ...... by photoaffinity crosslinking.

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Identification of the A2 adeno ...... by photoaffinity crosslinking.

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Identification of the A2 adeno ...... by photoaffinity crosslinking.

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Identification of the A2 adeno ...... by photoaffinity crosslinking.

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Identification of the A2 adeno ...... by photoaffinity crosslinking.

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Identification of the A2 adeno ...... by photoaffinity crosslinking.

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Identification of the A2 adeno ...... by photoaffinity crosslinking.

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Identification of the A2 adeno ...... by photoaffinity crosslinking.

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PNAS.86.17.6572

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Proceedings of the National Academy of Sciences of the United States of America

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Identification of the A2 adeno ...... by photoaffinity crosslinking.

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A J Hutchison

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G L Stiles

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K A Jacobson

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M Williams

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W W Barrington

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P2860

Cleavage of structural proteins during the assembly of the head of bacteriophage T4

A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding

125I-BW-A844U, an antagonist radioligand with high affinity and selectivity for adenosine A1 receptors, and 125I-azido-BW-A844U, a photoaffinity label.

Validation and statistical analysis of a computer modeling method for quantitative analysis of radioligand binding data for mixtures of pharmacological receptor subtypes.

Two distinct adenosine-sensitive sites on adenylate cyclase.

A [3H]amine congener of 1,3-dipropyl-8-phenylxanthine. A new radioligand for A2 adenosine receptors of human platelets.

[3H]xanthine amine congener of 1,3-dipropyl-8-phenylxanthine: an antagonist radioligand for adenosine receptors.

A new high affinity, iodinated adenosine receptor antagonist as a radioligand/photoaffinity crosslinking probe.

Identification of alpha-adrenergic receptors in human platelets by [3H]dihydroergocryptine binding.

Photoaffinity labels as pharmacological tools.

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6572-6576

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2771944

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