ORL1 receptor ligands: structure-activity relationships of 8-cycloalkyl-1-phenyl-1,3,8-triaza-spiro[4.5]decan-4-ones (Q40883724)

24 September 2017

title

ORL1 receptor ligands: structure-activity relationships of 8-cycloalkyl-1-phenyl-1,3,8-triaza-spiro[4.5]decan-4-ones (English)

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24 September 2017

Röver S

1

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24 September 2017

Wichmann J

2

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24 September 2017

Jenck F

3

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24 September 2017

Adam G

4

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24 September 2017

Cesura AM

5

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24 September 2017

language of work or name

English

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publication date

1 April 2000

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Bioorganic & Medicinal Chemistry Letters

24 September 2017

published in

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24 September 2017

volume

10

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24 September 2017

issue

8

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24 September 2017

page(s)

831-834

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Orphanin FQ: a neuropeptide that activates an opioidlike G protein-coupled receptor.

24 September 2017

cites work

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7 January 2021

Isolation and structure of the endogenous agonist of opioid receptor-like ORL1 receptor

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ORL1, a novel member of the opioid receptor family. Cloning, functional expression and localization

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Molecular cloning and tissue distribution of a putative member of the rat opioid receptor gene family that is not a mu, delta or kappa opioid receptor type

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7 January 2021

Recognition and activation of the opioid receptor-like ORL 1 receptor by nociceptin, nociceptin analogs and opioids

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7 January 2021

Orphanin FQ is a functional anti-opioid peptide.

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7 January 2021

Anti-hyperalgesic and anti-allodynic effects of intrathecal nociceptin/orphanin FQ in rats after spinal cord injury, peripheral nerve injury and inflammation

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Accelerated release and production of orphanin FQ in brain of chronic morphine tolerant rats

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7 January 2021

Orphanin FQ acts as an anxiolytic to attenuate behavioral responses to stress

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7 January 2021

8-acenaphthen-1-yl-1-phenyl-1,3,8-triaza-spiro[4.5]decan-4-one derivatives as orphanin FQ receptor agonists

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https://api.crossref.org/works/10.1016%2FS0960-894X%2800%2900111-6

7 January 2021

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

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Functional group contributions to drug-receptor interactions.

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10.1016/S0960-894X(00)00111-6

Identifiers

DOI

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24 September 2017

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