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J Med Chem
2002 Jul 18;4515:3210-21. doi: 10.1021/jm010461a.
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4D-QSAR analysis of a set of propofol analogues: mapping binding sites for an anesthetic phenol on the GABA(A) receptor.
Krasowski MD
,
Hong X
,
Hopfinger AJ
,
Harrison NL
.
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A training set of 27 propofol (2,6-diisopropylphenol) analogues was used to construct four-dimensional (4D) quantitative structure-activity relationship (QSAR) models for three screens of biological activity: loss of righting reflex (LORR) in tadpoles, enhancement of agonist activity at the gamma-aminobutyric acid type A (GABA(A)) receptor, and direct (agonist-independent) activation of the receptor. The three resulting 4D-QSAR models are almost identical in form, and all suggest three key ligand-receptor interaction sites. The formation of an intermolecular hydrogen bond involving the proton of the ligand -OH group is the most important binding interaction. A hydrophobic pocket binding interaction involving the six-substituent is the second most significant binding site, and a similar hydrophobic pocket binding interaction near the two-substituent is the third postulated binding site from the 4D-QSAR models. A test set of eight compounds was used to evaluate the tadpole LORR 4D-QSAR model. Those compounds highly congeneric to the training set compounds were accurately predicted. However, compounds exploring substituent sites and/or electronic structures different from the training set were less well-predicted. Overall, the results show a striking similarity between the models of the sites responsible for anesthesia and those mediating effects of the training set of propofol analogues on the GABA(A) receptor; it follows that the GABA(A) receptor is therefore the likely site of propofol's anesthetic action.
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12109905
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Abraham,
Role of hydrogen bonding in general anesthesia.
1991, Pubmed
Abraham,
Role of hydrogen bonding in general anesthesia.
1991,
Pubmed
Anderson,
Alpha-amino acid phenolic ester derivatives: novel water-soluble general anesthetic agents which allosterically modulate GABA(A) receptors.
2001,
Pubmed
,
Xenbase
Bai,
Distinct functional and pharmacological properties of tonic and quantal inhibitory postsynaptic currents mediated by gamma-aminobutyric acid(A) receptors in hippocampal neurons.
2001,
Pubmed
Bai,
The general anesthetic propofol slows deactivation and desensitization of GABA(A) receptors.
1999,
Pubmed
Barnard,
International Union of Pharmacology. XV. Subtypes of gamma-aminobutyric acidA receptors: classification on the basis of subunit structure and receptor function.
1998,
Pubmed
Beckstead,
Antagonism of inhalant and volatile anesthetic enhancement of glycine receptor function.
2001,
Pubmed
,
Xenbase
Bryson,
Propofol. An update of its use in anaesthesia and conscious sedation.
1995,
Pubmed
Concas,
The general anesthetic propofol enhances the function of gamma-aminobutyric acid-coupled chloride channel in the rat cerebral cortex.
1990,
Pubmed
Cooke,
Water-soluble propofol analogues with intravenous anaesthetic activity.
2001,
Pubmed
Cramer,
Comparative molecular field analysis (CoMFA). 1. Effect of shape on binding of steroids to carrier proteins.
1988,
Pubmed
Davies,
Modulation by general anaesthetics of rat GABAA receptors comprised of alpha 1 beta 3 and beta 3 subunits expressed in human embryonic kidney 293 cells.
1997,
Pubmed
Doenicke,
Pharmacokinetics and pharmacodynamics of propofol in a new solvent.
1997,
Pubmed
Doenicke,
Reducing pain during propofol injection: the role of the solvent.
1996,
Pubmed
Downes,
Contrasting effects of anesthetics in tadpole bioassays.
1996,
Pubmed
Franks,
Molecular and cellular mechanisms of general anaesthesia.
1994,
Pubmed
Hales,
The actions of propofol on inhibitory amino acid receptors of bovine adrenomedullary chromaffin cells and rodent central neurones.
1991,
Pubmed
Hansch,
Linear relationships between lipophilic character and biological activity of drugs.
1972,
Pubmed
Hara,
Propofol activates GABAA receptor-chloride ionophore complex in dissociated hippocampal pyramidal neurons of the rat.
1993,
Pubmed
Hara,
Enhancement by propofol of the gamma-aminobutyric acidA response in dissociated hippocampal pyramidal neurons of the rat.
1994,
Pubmed
James,
Synthesis, biological evaluation, and preliminary structure-activity considerations of a series of alkylphenols as intravenous anesthetic agents.
1980,
Pubmed
Janoff,
Correlation of general anesthetic potency with solubility in membranes.
1981,
Pubmed
Jones,
Modulation of the GABAA receptor by propofol is independent of the gamma subunit.
1995,
Pubmed
Krasowski,
Methionine 286 in transmembrane domain 3 of the GABAA receptor beta subunit controls a binding cavity for propofol and other alkylphenol general anesthetics.
2001,
Pubmed
Krasowski,
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.
2001,
Pubmed
,
Xenbase
Krasowski,
General anaesthetic actions on ligand-gated ion channels.
1999,
Pubmed
Langley,
Propofol. A review of its pharmacodynamic and pharmacokinetic properties and use as an intravenous anaesthetic.
1988,
Pubmed
Lingamaneni,
Anesthetic properties of 4-iodopropofol: implications for mechanisms of anesthesia.
2001,
Pubmed
,
Xenbase
McKernan,
Which GABAA-receptor subtypes really occur in the brain?
1996,
Pubmed
Orser,
Propofol modulates activation and desensitization of GABAA receptors in cultured murine hippocampal neurons.
1994,
Pubmed
Prankerd,
The use of oil-in-water emulsions as a vehicle for parenteral drug administration.
1990,
Pubmed
Ravi,
4D-QSAR analysis of a set of ecdysteroids and a comparison to CoMFA modeling.
2001,
Pubmed
Rudolph,
GABA(A) receptor subtypes: dissecting their pharmacological functions.
2001,
Pubmed
Sanna,
Actions of the general anesthetic propofol on recombinant human GABAA receptors: influence of receptor subunits.
1995,
Pubmed
,
Xenbase
Sanna,
Characterization of the electrophysiological and pharmacological effects of 4-iodo-2,6-diisopropylphenol, a propofol analogue devoid of sedative-anaesthetic properties.
1999,
Pubmed
,
Xenbase
Tanelian,
The role of the GABAA receptor/chloride channel complex in anesthesia.
1993,
Pubmed
Trapani,
Propofol analogues. Synthesis, relationships between structure and affinity at GABAA receptor in rat brain, and differential electrophysiological profile at recombinant human GABAA receptors.
1998,
Pubmed
,
Xenbase
Trapani,
Propofol in anesthesia. Mechanism of action, structure-activity relationships, and drug delivery.
2000,
Pubmed
Whiting,
Molecular and functional diversity of the expanding GABA-A receptor gene family.
1999,
Pubmed