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Neurochemicals for the Investigation of GABAC Receptors

Neurochemical research, 2010-12, Vol.35 (12), p.1970-1977

2010

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Modulation of Ionotropic GABA Receptors by Natural Products of Plant Origin

Advances in Pharmacology, 2006, Vol.54, p.285-316

2006

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Synthesis and biological evaluation of flavan-3-ol derivatives as positive modulators of GABAA receptors

Bioorganic & medicinal chemistry, 2009-10, Vol.17 (20), p.7156-7173

2009

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Flavan-3-ol esters: new agents for exploring modulatory sites on GABA(A) receptors

British journal of pharmacology, 2012-02, Vol.165 (4), p.965-977

2012

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Flavan‐3‐ol esters: new agents for exploring modulatory sites on GABAA receptors

British journal of pharmacology, 2012-02, Vol.165 (4), p.965-977

2012

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Neurochemicals for the investigation of GABA(C) receptors

Neurochemical research, 2010-12, Vol.35 (12), p.1970-1977

2010

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Medicinal Chemistry of ρ GABA C Receptors

Future medicinal chemistry, 2011-02, Vol.3 (2), p.197-209

2011

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Synthesis and activity of a potent N-methyl-D-aspartic acid agonist, trans-1-aminocyclobutane-1,3-dicarboxylic acid, and related phosphonic and carboxylic acids

Journal of medicinal chemistry, 1990-10, Vol.33 (10), p.2905-2915

1990

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(3-Aminocyclopentyl)methylphosphinic acids: novel GABA(C) receptor antagonists

Neuropharmacology, 2007-03, Vol.52 (3), p.779

2007

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(+)‐ and (‐)‐cis‐2‐Aminomethylcyclopropanecarboxylic Acids Show Opposite Pharmacology at Recombinant ρ1 and ρ2 GABAC Receptors

Journal of neurochemistry, 2000-12, Vol.75 (6), p.2602-2610

2000

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Convulsant actions of calycanthine

Toxicology and applied pharmacology, 2003-07, Vol.190 (1), p.58-64

2003

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Diastereoselective synthesis of (+/-)-(3-aminocyclopentane)alkylphosphinic acids, conformationally restricted analogues of GABA

Organic & biomolecular chemistry, 2006-01, Vol.4 (13), p.2642-2649

2006

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trans‐4‐Amino‐2‐methylbut‐2‐enoic acid (2‐MeTACA) and (±)‐trans‐2‐aminomethylcyclopropanecarboxylic acid ((±)‐TAMP) can differentiate rat ρ3 from human ρ1 and ρ2 recombinant GABAC receptors

British journal of pharmacology, 2002-02, Vol.135 (4), p.883-890

2002

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Flavan-3-ol derivatives are positive modulators of GABAA receptors with higher efficacy for the α2 subtype and anxiolytic action in mice

Neuropharmacology, 2008-10, Vol.55 (5), p.900-907

2008

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Flavan-3-ol esters: new agents for exploring modulatory sites on GABA sub(A) receptors

British journal of pharmacology, 2012-02, Vol.165 (4), p.965-977

2012

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GABAC Receptors as Drug Targets

Current drug targets. CNS & neurological disorders, 2003-08, Vol.2 (4), p.260-268

2003

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Idiospermuline, a Trimeric Pyrrolidinoindoline Alkaloid from the Seed of Idiospermum australiense

Journal of natural products (Washington, D.C.), 1995-08, Vol.58 (8), p.1200-1208

1995

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GABAC receptor antagonists differentiate between human ρ1 and ρ2 receptors expressed in Xenopus oocytes

European journal of pharmacology, 1998-09, Vol.357 (2-3), p.227-234

1998

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Neurochemicals for the Investigation of GABA sub(C) Receptors

Neurochemical research, 2010-12, Vol.35 (12), p.1970-1977

2010

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Guanidino Acids Act as ρ1 GABAC Receptor Antagonists

Neurochemical research, 2009-10, Vol.34 (10), p.1704-1711

2009

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trans ‐4‐Amino‐2‐methylbut‐2‐enoic acid (2‐MeTACA) and (±)‐ trans ‐2‐aminomethylcyclopropanecarboxylic acid ((±)‐TAMP) can differentiate rat ρ3 from human ρ1 and ρ2 recombinant GABA C receptors

British journal of pharmacology, 2009-02, Vol.135 (4), p.883-890

2009

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An improved, versatile synthesis of the GABAC antagonists (1,2,5,6-tetrahydropyridin-4-yl)methylphosphinic acid (TPMPA) and (piperidin-4-yl)methylphosphinic acid (P4MPA)

Perkin 1 : an international journal of organic and bio-organic chemistry, 2001 (19), p.2389-2392

2001

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Flavan-3-ol derivatives are positive modulators of GABA(A) receptors with higher efficacy for the alpha(2) subtype and anxiolytic action in mice

Neuropharmacology, 2008-10, Vol.55 (5), p.900-907

2008

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Structural analogues of ZAPA as GABA A agonists

Neurochemistry international, 1997-06, Vol.30 (6), p.583-591

1997

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(3-Aminocyclopentyl)methylphosphinic acids: Novel GABAC receptor antagonists

Neuropharmacology, 2007-03, Vol.52 (3), p.779-787

2007

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Neurochemicals for the Investigation of GABAC Receptors

Modulation of Ionotropic GABA Receptors by Natural Products of Plant Origin

Synthesis and biological evaluation of flavan-3-ol derivatives as positive modulators of GABAA receptors

Flavan-3-ol esters: new agents for exploring modulatory sites on GABA(A) receptors

Flavan‐3‐ol esters: new agents for exploring modulatory sites on GABAA receptors

Neurochemicals for the investigation of GABA(C) receptors

Medicinal Chemistry of ρ GABA C Receptors

Synthesis and activity of a potent N-methyl-D-aspartic acid agonist, trans-1-aminocyclobutane-1,3-dicarboxylic acid, and related phosphonic and carboxylic acids

(3-Aminocyclopentyl)methylphosphinic acids: novel GABA(C) receptor antagonists

(+)‐ and (‐)‐cis‐2‐Aminomethylcyclopropanecarboxylic Acids Show Opposite Pharmacology at Recombinant ρ1 and ρ2 GABAC Receptors

Convulsant actions of calycanthine

Diastereoselective synthesis of (+/-)-(3-aminocyclopentane)alkylphosphinic acids, conformationally restricted analogues of GABA

trans‐4‐Amino‐2‐methylbut‐2‐enoic acid (2‐MeTACA) and (±)‐trans‐2‐aminomethylcyclopropanecarboxylic acid ((±)‐TAMP) can differentiate rat ρ3 from human ρ1 and ρ2 recombinant GABAC receptors

Flavan-3-ol derivatives are positive modulators of GABAA receptors with higher efficacy for the α2 subtype and anxiolytic action in mice

Flavan-3-ol esters: new agents for exploring modulatory sites on GABA sub(A) receptors

GABAC Receptors as Drug Targets

Idiospermuline, a Trimeric Pyrrolidinoindoline Alkaloid from the Seed of Idiospermum australiense

GABAC receptor antagonists differentiate between human ρ1 and ρ2 receptors expressed in Xenopus oocytes

Neurochemicals for the Investigation of GABA sub(C) Receptors

Guanidino Acids Act as ρ1 GABAC Receptor Antagonists

trans ‐4‐Amino‐2‐methylbut‐2‐enoic acid (2‐MeTACA) and (±)‐ trans ‐2‐aminomethylcyclopropanecarboxylic acid ((±)‐TAMP) can differentiate rat ρ3 from human ρ1 and ρ2 recombinant GABA C receptors

An improved, versatile synthesis of the GABAC antagonists (1,2,5,6-tetrahydropyridin-4-yl)methylphosphinic acid (TPMPA) and (piperidin-4-yl)methylphosphinic acid (P4MPA)

Flavan-3-ol derivatives are positive modulators of GABA(A) receptors with higher efficacy for the alpha(2) subtype and anxiolytic action in mice

Structural analogues of ZAPA as GABA A agonists

(3-Aminocyclopentyl)methylphosphinic acids: Novel GABAC receptor antagonists

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