4-amino-6-alkyloxy-2-alkylthiopyrimidine derivatives as novel non-nucleoside agonists for the adenosine A1 receptor.

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4-amino-6-alkyloxy-2-alkylthiopyrimidine derivatives as novel non-nucleoside agonists for the adenosine A1 receptor.

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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

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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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2016年學術文章

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4-amino-6-alkyloxy-2-alkylthio ...... for the adenosine A1 receptor.

@en

4-amino-6-alkyloxy-2-alkylthio ...... for the adenosine A1 receptor.

@nl

type

Item

label

4-amino-6-alkyloxy-2-alkylthio ...... for the adenosine A1 receptor.

@en

4-amino-6-alkyloxy-2-alkylthio ...... for the adenosine A1 receptor.

@nl

altLabel

4-amino-6-alkyloxy-2-alkylthio ...... s for the adenosine A1receptor

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prefLabel

4-amino-6-alkyloxy-2-alkylthio ...... for the adenosine A1 receptor.

@en

4-amino-6-alkyloxy-2-alkylthio ...... for the adenosine A1 receptor.

@nl

P1476

4-amino-6-alkyloxy-2-alkylthio ...... for the adenosine A1 receptor.

@en

P2093

Antonia Sacchi

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Federico Da Settimo

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Giovanni Greco

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Maria Letizia Trincavelli

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Sabrina Taliani

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Sonia Laneri

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P2860

Adenosine receptors as therapeutic targets

Recent developments in adenosine receptor ligands and their potential as novel drugs

International Union of Basic and Clinical Pharmacology. LXXXI. Nomenclature and classification of adenosine receptors--an update

Signalling from adenosine receptors to mitogen-activated protein kinases.

Regadenoson: a new myocardial stress agent.

Synthesis and biological evaluation of imidazo[1,2-a]pyrimidines and imidazo[1,2-a]pyridines as new inhibitors of the Wnt/β-catenin signaling.

A novel nonribose agonist, LUF5834, engages residues that are distinct from those of adenosine-like ligands to activate the adenosine A(2a) receptor.

Synthesis, adenosine receptor binding and 3D-QSAR of 4-substituted 2-(2'-furyl)-1,2,4-triazolo[1,5-a]quinoxalines.

Coupling of the human A1 adenosine receptor to different heterotrimeric G proteins: evidence for agonist-specific G protein activation.

New, non-adenosine, high-potency agonists for the human adenosine A2B receptor with an improved selectivity profile compared to the reference agonist N-ethylcarboxamidoadenosine.

P304

724-729

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P31

scholarly article

P356

10.1111/CBDD.12801

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P433

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P478

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

P50

P577

2016-06-10T00:00:00Z

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P698

27282729

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