(Q44485803)

3 December 2017

title

Conformation by NMR of two tetralin-based receptor ligands (English)

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3 December 2017

2

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3 December 2017

3

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3 December 2017

Giuseppe Gatti

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3 December 2017

publication date

1 July 2003

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3 December 2017

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3 December 2017

volume

58

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3 December 2017

issue

7

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3 December 2017

page(s)

469-476

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Melatonin receptor antagonists that differentiate between the human Mel1a and Mel1b recombinant subtypes are used to assess the pharmacological profile of the rabbit retina ML1 presynaptic heteroreceptor

3 December 2017

cites work

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https://api.crossref.org/works/10.1016%2FS0014-827X%2803%2900064-8

2-Amido-8-methoxytetralins: a series of nonindolic melatonin-like agents

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-827X%2803%2900064-8

A novel phenylaminotetralin (PAT) recognizes histamine H1 receptors and stimulates dopamine synthesis in vivo in rat brain

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-827X%2803%2900064-8

Synthesis, evaluation, and comparative molecular field analysis of 1-phenyl-3-amino-1,2,3,4-tetrahydronaphthalenes as ligands for histamine H(1) receptors

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-827X%2803%2900064-8

Synthesis and pharmacological evaluation of 1-phenyl-3-amino-1,2,3,4-tetrahydronaphthalenes as ligands for a novel receptor with sigma-like neuromodulatory activity

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-827X%2803%2900064-8

The chronobiotic properties of melatonin

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-827X%2803%2900064-8

Mapping the melatonin receptor. 6. Melatonin agonists and antagonists derived from 6H-isoindolo[2,1-a]indoles, 5,6-dihydroindolo[2,1-a]isoquinolines, and 6,7-dihydro-5H-benzo[c]azepino[2,1-a]indoles

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-827X%2803%2900064-8

2-N-acylaminoalkylindoles: design and quantitative structure-activity relationship studies leading to MT2-selective melatonin antagonists

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-827X%2803%2900064-8

Ersatz von an Stickstoff gebundenen Wasserstoffatomen durch die Methylgruppe mit Hülfe von Formaldehyd

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-827X%2803%2900064-8

Pharmacological characterization of the human melatonin Mel1a receptor following stable transfection into NIH3T3 cells

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-827X%2803%2900064-8

Ligand efficacy and potency at recombinant human MT2 melatonin receptors: evidence for agonist activity of some mt1-antagonists

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-827X%2803%2900064-8

2-[N-Acylamino(C1-C3)alkyl]indoles as MT1 melatonin receptor partial agonists, antagonists, and putative inverse agonists.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-827X%2803%2900064-8

Calibration of the angular dependence of the amide proton-C alpha proton coupling constants, 3JHN alpha, in a globular protein. Use of 3JHN alpha for identification of helical secondary structure

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-827X%2803%2900064-8

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-827X%2803%2900064-8

10.1016/S0014-827X(03)00064-8

7 January 2021

Identifiers

DOI

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3 December 2017

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