Novel GABAB receptor positive modulators: a patent survey

Importance of the field: Positive allosteric modulators of GABAB receptors may have a similar potential as positive modulators of GABAA receptors, the benzodiazepines discovered in 1957. The discovery of positive allosteric modulators of GABAB receptors at Novartis in Basel in 2000 opened the way to search for compounds, which activate GABAB receptors without the drawbacks of full agonists, such as desensitization, tolerance, muscle-relaxant effects, hypothermia, and central and gastrointestinal side effects. Areas covered in this review: Numerous animal experiments point out that several indications can be addressed with positive modulators of GABAB receptors, such as depression, anxiety, schizophrenia, neuropathic and chronic pain and treatment of craving for drugs of abuse, such as alcohol, cocaine and nicotine. Peripherally acting compounds may be valuable drugs for the treatment of gastroesophageal reflux disease and irritable bowel syndrome. What the reader will gain: An overview on 19 patents in this field, of the different scaffolds for positive modulators of GABAB receptors and of the major players in the field. Take home message: The search for subtype selective benzodiazepine receptor ligands has proved to be extremely difficult. Positive modulators of GABAB receptors may provide novel anxiolytic drugs faster.

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[6]  L. Prézeau,et al.  The Heptahelical Domain of GABAB2 Is Activated Directly by CGP7930, a Positive Allosteric Modulator of the GABAB Receptor* , 2004, Journal of Biological Chemistry.

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[14]  A. Markou,et al.  Positive Modulation of GABAB Receptors Decreased Nicotine Self-Administration and Counteracted Nicotine-Induced Enhancement of Brain Reward Function in Rats , 2008, Journal of Pharmacology and Experimental Therapeutics.

[15]  G. Gessa,et al.  Reduction of alcohol's reinforcing and motivational properties by the positive allosteric modulator of the GABA(B) receptor, BHF177, in alcohol-preferring rats. , 2009, Alcoholism, clinical and experimental research.

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[19]  P. Malherbe,et al.  Efficient One-Pot Synthesis of the GABAB Positive Allosteric Modulator (R,S)-5,7-Di-tert-butyl-3-hydroxy-3-trifluoromethyl-3H-benzofuran-2-one , 2008 .

[20]  A. Lawrence,et al.  The GABA(B) receptor allosteric modulator CGP7930, like baclofen, reduces operant self-administration of ethanol in alcohol-preferring rats. , 2006, Neuropharmacology.

[21]  W. Froestl,et al.  Syntheses and optimization of new GS39783 analogues as positive allosteric modulators of GABA B receptors. , 2007, Bioorganic & medicinal chemistry letters.

[22]  M. Filip,et al.  Effects of GABAB receptor ligands in animal tests of depression and anxiety. , 2007, Pharmacological reports : PR.

[23]  J. Mosbacher,et al.  Point Mutations in the Transmembrane Region of GABAB2 Facilitate Activation by the Positive Modulator N,N′-Dicyclopentyl-2-methylsulfanyl-5-nitro-pyrimidine-4,6-diamine (GS39783) in the Absence of the GABAB1 Subunit , 2006, Molecular Pharmacology.

[24]  S. Urwyler,et al.  N,N′-Dicyclopentyl-2-methylsulfanyl-5-nitro-pyrimidine-4,6-diamine (GS39783) and Structurally Related Compounds: Novel Allosteric Enhancers of γ-Aminobutyric AcidB Receptor Function , 2003, Journal of Pharmacology and Experimental Therapeutics.

[25]  Christer Alstermark,et al.  Synthesis and pharmacological evaluation of novel gamma-aminobutyric acid type B (GABAB) receptor agonists as gastroesophageal reflux inhibitors. , 2008, Journal of medicinal chemistry.

[26]  Jacobson,et al.  (R)-(3-Amino-2-fluoropropyl) Phosphinic Acid (AZD3355), a Novel GABAB Receptor Agonist, Inhibits Transient Lower Esophageal Sphincter Relaxation through a Peripheral Mode of Action , 2009, Journal of Pharmacology and Experimental Therapeutics.

[27]  S. Urwyler,et al.  Positive allosteric modulation of native and recombinant gamma-aminobutyric acid(B) receptors by 2,6-Di-tert-butyl-4-(3-hydroxy-2,2-dimethyl-propyl)-phenol (CGP7930) and its aldehyde analog CGP13501. , 2001, Molecular pharmacology.

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[29]  G. Gessa,et al.  Reducing effect of the positive allosteric modulator of the GABAB receptor, GS39783, on alcohol self-administration in alcohol-preferring rats , 2007, Psychopharmacology.

[30]  Mark A. Smith,et al.  Effects of positive allosteric modulators of the GABAB receptor on cocaine self-administration in rats , 2004, Psychopharmacology.

[31]  J. Cryan,et al.  Evaluation of the anxiolytic-like profile of the GABAB receptor positive modulator CGP7930 in rodents , 2008, Neuropharmacology.

[32]  A. Lawrence,et al.  The GABAB receptor allosteric modulator CGP7930, like baclofen, reduces operant self-administration of ethanol in alcohol-preferring rats , 2006, Neuropharmacology.

[33]  J. Cryan,et al.  GABAB Receptor-Positive Modulation-Induced Blockade of the Rewarding Properties of Nicotine Is Associated with a Reduction in Nucleus Accumbens ΔFosB Accumulation , 2007, Journal of Pharmacology and Experimental Therapeutics.

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[35]  S. Urwyler,et al.  Receptor activation involving positive allosteric modulation, unlike full agonism, does not result in GABAB receptor desensitization , 2008, Neuropharmacology.

[36]  M. Pangalos,et al.  Unravelling the unusual signalling properties of the GABA(B) receptor. , 2004, Biochemical pharmacology.

[37]  T. Schwartz,et al.  Allosteric enhancers, allosteric agonists and ago-allosteric modulators: where do they bind and how do they act? , 2007, Trends in pharmacological sciences.

[38]  L. Prézeau,et al.  Allosteric Modulators of GABAB Receptors: Mechanism of Action and Therapeutic Perspective , 2007, Current neuropharmacology.