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Hydrocarbon molar water solubility predicts NMDA vs. GABAA receptor modulation.

Hydrocarbon molar water solubility predicts NMDA vs. GABAA receptor modulation.

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Anesthetic synergy between two n-alkanes.Anesthetic-sensitive ion channel modulation is associated with a molar water solubility cut-off

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Hydrocarbon molar water solubility predicts NMDA vs. GABAA receptor modulation.

http://www.wikidata.org/entity/Q34587545

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2014 nî lūn-bûn

@nan

2014 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի նոյեմբերին հրատարակված գիտական հոդված

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年论文

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Hydrocarbon molar water solubility predicts NMDA vs. GABAA receptor modulation.

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Hydrocarbon molar water solubility predicts NMDA vs. GABAA receptor modulation.

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Hydrocarbon molar water solubility predicts NMDA vs. GABAA receptor modulation.

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Hydrocarbon molar water solubility predicts NMDA vs. GABAA receptor modulation.

@ast

Hydrocarbon molar water solubility predicts NMDA vs. GABAA receptor modulation.

@en

Hydrocarbon molar water solubility predicts NMDA vs. GABAA receptor modulation.

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Hydrocarbon molar water solubility predicts NMDA vs. GABAA receptor modulation.

@ast

Hydrocarbon molar water solubility predicts NMDA vs. GABAA receptor modulation.

@en

Hydrocarbon molar water solubility predicts NMDA vs. GABAA receptor modulation.

@nl

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2050-6511-15-62

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BMC pharmacology & toxicology

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Hydrocarbon molar water solubility predicts NMDA vs. GABAA receptor modulation.

@en

P2093

Robert J Brosnan

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Trung L Pham

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P2860

The anticonvulsant MK-801 is a potent N-methyl-D-aspartate antagonist

Exploring volatile general anesthetic binding to a closed membrane-bound bacterial voltage-gated sodium channel via computation

Stereoselective effects of etomidate optical isomers on gamma-aminobutyric acid type A receptors and animals

The actions of ether, alcohol and alkane general anaesthetics on GABAA and glycine receptors and the effects of TM2 and TM3 mutations

Hypothesis: volatile anesthetics produce immobility by acting on two sites approximately five carbon atoms apart.

Effects of gaseous anesthetics nitrous oxide and xenon on ligand-gated ion channels. Comparison with isoflurane and ethanol.

General anesthetic potencies of a series of propofol analogs correlate with potency for potentiation of gamma-aminobutyric acid (GABA) current at the GABA(A) receptor but not with lipid solubility.

Gamma-aminobutyric acid type A receptor alpha 4 subunit knockout mice are resistant to the amnestic effect of isoflurane.

Multiple binding sites for the general anesthetic isoflurane identified in the nicotinic acetylcholine receptor transmembrane domain.

Anesthetic binding in a pentameric ligand-gated ion channel: GLIC

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2050-6511-15-62

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scholarly article

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10.1186/2050-6511-15-62

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15

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2014-11-19T00:00:00Z

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