(Q43645245)

25 November 2017

title

alpha-Keto heterocycle inhibitors of fatty acid amide hydrolase: carbonyl group modification and alpha-substitution (English)

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25 November 2017

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D L Boger

1

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25 November 2017

H Miyauchi

series ordinal

2

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25 November 2017

M P Hedrick

series ordinal

3

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25 November 2017

language of work or name

English

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publication date

1 June 2001

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Bioorganic & Medicinal Chemistry Letters

25 November 2017

published in

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25 November 2017

volume

11

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25 November 2017

issue

12

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25 November 2017

page(s)

1517-1520

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Isolation and structure of a brain constituent that binds to the cannabinoid receptor

25 November 2017

cites work

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Chemical characterization of a family of brain lipids that induce sleep

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Characterization of the hypnotic properties of oleamide.

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Modification of 5-HT2 receptor mediated behaviour in the rat by oleamide and the role of cannabinoid receptors.

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Anandamide may mediate sleep induction

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Brain lipids that induce sleep are novel modulators of 5-hydroxytrypamine receptors

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Unique allosteric regulation of 5-hydroxytryptamine receptor-mediated signal transduction by oleamide

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7 January 2021

Structural requirements for 5-HT2A and 5-HT1A serotonin receptor potentiation by the biologically active lipid oleamide

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The endogenous lipid oleamide activates serotonin 5-HT7 neurons in mouse thalamus and hypothalamus

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7 January 2021

Stereoselective modulatory actions of oleamide on GABA(A) receptors and voltage-gated Na(+) channels in vitro: a putative endogenous ligand for depressant drug sites in CNS.

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Anesthetic-like interaction of the sleep-inducing lipid oleamide with voltage-gated sodium channels in mammalian brain

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7 January 2021

The sleep-inducing lipid oleamide deconvolutes gap junction communication and calcium wave transmission in glial cells

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7 January 2021

Chemical requirements for inhibition of gap junction communication by the biologically active lipid oleamide

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7 January 2021

Vanilloid receptors on sensory nerves mediate the vasodilator action of anandamide

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The endogenous lipid anandamide is a full agonist at the human vanilloid receptor (hVR1)

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7 January 2021

Pain modulation by release of the endogenous cannabinoid anandamide

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7 January 2021

Molecular characterization of an enzyme that degrades neuromodulatory fatty-acid amides

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7 January 2021

Molecular characterization of human and mouse fatty acid amide hydrolases

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7 January 2021

An endogenous sleep-inducing compound is a novel competitive inhibitor of fatty acid amide hydrolase

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7 January 2021

Trifluoromethyl ketone inhibitors of fatty acid amide hydrolase: a probe of structural and conformational features contributing to inhibition

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7 January 2021

Exceptionally potent inhibitors of fatty acid amide hydrolase: the enzyme responsible for degradation of endogenous oleamide and anandamide

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7 January 2021

Fatty acid amide hydrolase substrate specificity

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7 January 2021

10.1016/S0960-894X(01)00211-6

Identifiers

DOI

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25 November 2017

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