(Q30326718)

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The identification of novel structural compound classes exhibiting high affinity for neuronal nicotinic acetylcholine receptors and analgesic efficacy in preclinical models of pain.

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Europe PubMed Central

PubMed publication ID

18 June 2017

The identification of novel structural compound classes exhibiting high affinity for neuronal nicotinic acetylcholine receptors and analgesic efficacy in preclinical models of pain. (English)

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Europe PubMed Central

PubMed publication ID

18 June 2017

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M D Meyer

1

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Europe PubMed Central

PubMed publication ID

18 June 2017

M W Decker

2

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Europe PubMed Central

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18 June 2017

L E Rueter

3

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Europe PubMed Central

PubMed publication ID

18 June 2017

D J Anderson

4

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Europe PubMed Central

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18 June 2017

M J Dart

5

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Europe PubMed Central

PubMed publication ID

18 June 2017

K H Kim

6

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18 June 2017

J P Sullivan

7

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18 June 2017

M Williams

8

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18 June 2017

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publication date

1 March 2000

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18 June 2017

European Journal of Pharmacology

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18 June 2017

393

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18 June 2017

1-3

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18 June 2017

171-177

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PubMed publication ID

18 June 2017

Novel 3-Pyridyl ethers with subnanomolar affinity for central neuronal nicotinic acetylcholine receptors

1 reference

https://api.crossref.org/works/10.1016%2FS0014-2999%2800%2900041-8

7 January 2021

Broad-spectrum, non-opioid analgesic activity by selective modulation of neuronal nicotinic acetylcholine receptors

1 reference

https://api.crossref.org/works/10.1016%2FS0014-2999%2800%2900041-8

7 January 2021

Mono- and disubstituted-3,8-diazabicyclo[3.2.1]octane derivatives as analgesics structurally related to epibatidine: synthesis, activity, and modeling.

1 reference

https://api.crossref.org/works/10.1016%2FS0014-2999%2800%2900041-8

7 January 2021

Structure and activity of acetylcholine

1 reference

https://api.crossref.org/works/10.1016%2FS0014-2999%2800%2900041-8

7 January 2021

Role of the nucleus raphe magnus in antinociception produced by ABT-594: immediate early gene responses possibly linked to neuronal nicotinic acetylcholine receptors on serotonergic neurons.

1 reference

https://api.crossref.org/works/10.1016%2FS0014-2999%2800%2900041-8

7 January 2021

The role of neuronal nicotinic acetylcholine receptors in antinociception: effects of ABT-594.

1 reference

https://api.crossref.org/works/10.1016%2FS0014-2999%2800%2900041-8

7 January 2021

Cation-pi interactions in chemistry and biology: a new view of benzene, Phe, Tyr, and Trp

1 reference

https://api.crossref.org/works/10.1016%2FS0014-2999%2800%2900041-8

7 January 2021

The emerging three-dimensional structure of a receptor. The nicotinic acetylcholine receptor

1 reference

https://api.crossref.org/works/10.1016%2FS0014-2999%2800%2900041-8

7 January 2021

Synthesis and biological characterization of pyridohomotropanes. Structure-activity relationships of conformationally restricted nicotinoids

1 reference

https://api.crossref.org/works/10.1016%2FS0014-2999%2800%2900041-8

7 January 2021

2-, 5-, and 6-Halo-3-(2(S)-azetidinylmethoxy)pyridines: synthesis, affinity for nicotinic acetylcholine receptors, and molecular modeling.

1 reference

https://api.crossref.org/works/10.1016%2FS0014-2999%2800%2900041-8

7 January 2021

Reduced antinociception in mice lacking neuronal nicotinic receptor subunits

1 reference

https://api.crossref.org/works/10.1016%2FS0014-2999%2800%2900041-8

7 January 2021

Nicotinic acetylcholine receptor at 4.6 A resolution: transverse tunnels in the channel wall.

1 reference

https://api.crossref.org/works/10.1016%2FS0014-2999%2800%2900041-8

7 January 2021

Molecular recognition in nicotinic acetylcholine receptors: the importance of pi-cation interactions

1 reference

https://api.crossref.org/works/10.1016%2FS0014-2999%2800%2900041-8

7 January 2021

The ensemble approach to distance geometry: application to the nicotinic pharmacophore

1 reference

https://api.crossref.org/works/10.1016%2FS0014-2999%2800%2900041-8

7 January 2021

Anionic residue in the alpha-subunit of the nicotinic acetylcholine receptor contributing to subunit assembly and ligand binding

1 reference

https://api.crossref.org/works/10.1016%2FS0014-2999%2800%2900041-8

7 January 2021

Solid state NMR studies of ligands bound to the nicotinic acetylcholine receptor

1 reference

https://api.crossref.org/works/10.1016%2FS0014-2999%2800%2900041-8

7 January 2021

From ab initio quantum mechanics to molecular neurobiology: a cation-pi binding site in the nicotinic receptor

1 reference

https://api.crossref.org/works/10.1016%2FS0014-2999%2800%2900041-8

7 January 2021

An Epoxide Rearrangement - Radical Rearrangement Approach to 6-Substituted 2-Azabicyclo[2.2.1]-5-heptenes: Synthesis of an Epibatidine Analogue

1 reference

https://api.crossref.org/works/10.1016%2FS0014-2999%2800%2900041-8

7 January 2021

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10.1016/S0014-2999(00)00041-8

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Europe PubMed Central

PubMed publication ID

18 June 2017

release_puc5kc6nqbfvfhqacji3h2r72e

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https://api.fatcat.wiki/v0/release/puc5kc6nqbfvfhqacji3h2r72e

24 November 2022

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18 June 2017

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