Development of Radiolabeled Ligands Targeting the Glutamate Binding Site of the N-Methyl-d-aspartate Receptor as Potential Imaging Agents for Brain.

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Structural basis of subunit selectivity for competitive NMDA receptor antagonists with preference for GluN2A over GluN2B subunits.Synthesis of l -Tricholomic Acid Analogues and Pharmacological Characterization at Ionotropic Glutamate Receptors

P2860

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P2860

Development of Radiolabeled Ligands Targeting the Glutamate Binding Site of the N-Methyl-d-aspartate Receptor as Potential Imaging Agents for Brain.

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http://www.wikidata.org/entity/Q48128197

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2016 nî lūn-bûn

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2016年の論文

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

@zh-hans

2016年学术文章

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2016年学术文章

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2016年學術文章

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2016年學術文章

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name

Development of Radiolabeled Li ...... tial Imaging Agents for Brain.

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Development of Radiolabeled Li ...... tial Imaging Agents for Brain.

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type

Item

label

Development of Radiolabeled Li ...... tial Imaging Agents for Brain.

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Development of Radiolabeled Li ...... tial Imaging Agents for Brain.

@nl

prefLabel

Development of Radiolabeled Li ...... tial Imaging Agents for Brain.

@en

Development of Radiolabeled Li ...... tial Imaging Agents for Brain.

@nl

P1476

Development of Radiolabeled Li ...... tial Imaging Agents for Brain.

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P2093

Andrew G Horti

http://www.w3.org/2001/XMLSchema#string

Carlo De Micheli

http://www.w3.org/2001/XMLSchema#string

Catherine A Foss

http://www.w3.org/2001/XMLSchema#string

Kasper B Hansen

http://www.w3.org/2001/XMLSchema#string

Lucia Tamborini

http://www.w3.org/2001/XMLSchema#string

Martin G Pomper

http://www.w3.org/2001/XMLSchema#string

Ronnie C Mease

http://www.w3.org/2001/XMLSchema#string

Stephen F Traynelis

http://www.w3.org/2001/XMLSchema#string

Ying Chen

http://www.w3.org/2001/XMLSchema#string

P2860

Substituted pyrazoles as hepatoselective HMG-CoA reductase inhibitors: discovery of (3R,5R)-7-[2-(4-fluoro-phenyl)-4-isopropyl-5-(4-methyl-benzylcarbamoyl)-2H-pyrazol-3-yl]-3,5-dihydroxyheptanoic acid (PF-3052334) as a candidate for the treatment of

Structural Determinants of Agonist Efficacy at the Glutamate Binding Site of N-Methyl-D-Aspartate Receptors

Relationship between the inhibition constant (K1) and the concentration of inhibitor which causes 50 per cent inhibition (I50) of an enzymatic reaction

5-Phosphonomethylquinoxalinediones as competitive NMDA receptor antagonists with a preference for the human 1A/2A, rather than 1A/2B receptor composition.

Equilibrium constants for (R)-[(S)-1-(4-bromo-phenyl)-ethylamino]-(2,3-dioxo-1,2,3,4-tetrahydroquinoxalin-5-yl)-methyl]-phosphonic acid (NVP-AAM077) acting at recombinant NR1/NR2A and NR1/NR2B N-methyl-D-aspartate receptors: Implications for studies

New advances in NMDA receptor pharmacology.

Selected PET Radioligands for Ion Channel Linked Neuroreceptor Imaging: Focus on GABA, NMDA and nACh Receptors

N'-3-(Trifluoromethyl)phenyl Derivatives of N-Aryl-N'-methylguanidines as Prospective PET Radioligands for the Open Channel of the N-Methyl-d-aspartate (NMDA) Receptor: Synthesis and Structure-Affinity Relationships

NMDA receptors in nervous system diseases.

The molecular basis of NMDA receptor subtypes: native receptor diversity is predicted by subunit composition.

P304

11110-11119

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scholarly article

P356

10.1021/ACS.JMEDCHEM.6B01344

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English

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P478

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P50

Paola Conti

Andrea Pinto

P577

2016-12-06T00:00:00Z

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P698

28002957

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P932

5484777

http://www.w3.org/2001/XMLSchema#string

Development of Radiolabeled Ligands Targeting the Glutamate Binding Site of the N-Methyl-d-aspartate Receptor as Potential Imaging Agents for Brain.

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P2860

P2860

Development of Radiolabeled Ligands Targeting the Glutamate Binding Site of the N-Methyl-d-aspartate Receptor as Potential Imaging Agents for Brain.

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