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In vivo efficacy in airway disease models of N-(3,5-dichloropyrid-4-yl)-[1-(4-fluorobenzyl)-5-hydroxy-indole-3-yl]-glyoxylic acid amide (AWD 12-281), a selective phosphodiesterase 4 inhibitor for inhaled administration

The Journal of pharmacology and experimental therapeutics, 2003-10, Vol.307 (1), p.373

2003

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P.1.c.021 Effect of phosphodiesterase 2A inhibition on striatal dopamine in a microdialysis study and its reflection in dopamine-associated effects in animal models

European neuropsychopharmacology, 2011, Vol.21, p.S265-S265

2011

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P.1.g.012 The pro-cognitive profile of the phosphodiesterase 2A inhibitor BCR909 highlights its utility as a novel treatment for diseases with cognitive decline

European neuropsychopharmacology, 2011, Vol.21, p.S335-S336

2011

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5-(4-Hydroxy-6-methyl-2-oxo-2H-pyran-3-yl)-7-phenyl-2,3,6,7-tetrahydro-1,4-thiazepines as compounds with high affinity at the benzodiazepine binding site on GABA(A) receptors

Pharmazie, 2011-02, Vol.66 (2), p.98-104

2011

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Synthesis, Pharmacology, and Structure-Activity Relationships of Novel Imidazolones and Pyrrolones as Modulators of GABA sub(A) Receptors

Journal of medicinal chemistry, 2006-03, Vol.49 (6), p.1855-1866

2006

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Targeting PDE10A in schizophrenia

Drugs of the future, 2012, Vol.37 (8), p.577

2012

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Targeting PDE10A in schizophrenia

Drugs of the future, 2012-08, Vol.37 (8), p.577

2012

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ChemInform Abstract: 5-(4-Hydroxy-6-methyl-2-oxo-2H-pyran-3-yl) -7-phenyl-2,3,6,7-tetrahydro-1,4-thiazepines as Compounds with High Affinity at the Benzodiazepine Binding Site on GABAA Receptors

ChemInform, 2011-06, Vol.42 (25), p.no-no

2011

Volltextzugriff (PDF)

ChemInform Abstract: 5‐(4‐Hydroxy‐6‐methyl‐2‐oxo‐2H‐pyran‐3‐yl) ‐7‐phenyl‐2,3,6,7‐tetrahydro‐1,4‐thiazepines as Compounds with High Affinity at the Benzodiazepine Binding Site on GABA A Receptors

ChemInform, 2011-06, Vol.42 (25)

2011

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1,5-Disubstituted Indazol-3-ols with Anti-Inflammatory Activity

Archiv der Pharmazie (Weinheim), 1998-01, Vol.331 (1), p.13-21

1998

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ChemInform Abstract: Indazole-3-oles and Indazole-2-ones with Antiinflammatory Activity

ChemInform, 2001-02, Vol.32 (7), p.no-no

2001

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ChemInform Abstract: 1,5-Disubstituted Indazol-3-ols with anti-Inflammatory Activity

ChemInform, 1998-05, Vol.29 (18), p.no-no

1998

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Lost Earnings and Nonmedical Expenses of Pediatric Hospitalizations

Pediatrics (Evanston), 2018-09, Vol.142 (3)

2018

Volltextzugriff (PDF)

Highly Potent, Selective, and Orally Active Phosphodiesterase 10A Inhibitors

Journal of medicinal chemistry, 2011-11, Vol.54 (21), p.7621-7638

2011

Volltextzugriff (PDF)

48. Sertoli Leydig Cell Tumor Presenting With Elevated Adrenal Markers in an Adolescent

Journal of pediatric & adolescent gynecology, 2019-04, Vol.32 (2), p.213-214

2019

Volltextzugriff (PDF)

Discovery of Imidazo[1,5-a]pyrido[3,2-e]pyrazines as a New Class of Phosphodiesterase 10A Inhibitiors

Journal of medicinal chemistry, 2010-06, Vol.53 (11), p.4399-4411

2010

Volltextzugriff (PDF)

Invasive Ductal Carcinoma in A 46,XY Partial Androgen Insensitivity Syndrome Patient on Hormone Therapy

Journal of pediatric & adolescent gynecology, 2013-04, Vol.26 (2), p.e52-e52

2013

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Rope Swing Injuries Resulting in Vulvar Trauma

Journal of pediatric & adolescent gynecology, 2013-04, Vol.26 (2), p.e61-e62

2013

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Novel triazines as potent and selective phosphodiesterase 10A inhibitors

Bioorganic & medicinal chemistry letters, 2012-09, Vol.22 (18), p.5876-5884

2012

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In vivo efficacy in airway disease models of N-(3,5-dichloropyrid-4-yl)-[1-(4-fluorobenzyl)-5-hydroxy-indole-3-yl]-glyoxylic acid amide (AWD 12-281), a selective phosphodiesterase 4 inhibitor for inhaled administration

P.1.c.021 Effect of phosphodiesterase 2A inhibition on striatal dopamine in a microdialysis study and its reflection in dopamine-associated effects in animal models

P.1.g.012 The pro-cognitive profile of the phosphodiesterase 2A inhibitor BCR909 highlights its utility as a novel treatment for diseases with cognitive decline

5-(4-Hydroxy-6-methyl-2-oxo-2H-pyran-3-yl)-7-phenyl-2,3,6,7-tetrahydro-1,4-thiazepines as compounds with high affinity at the benzodiazepine binding site on GABA(A) receptors

Synthesis, Pharmacology, and Structure-Activity Relationships of Novel Imidazolones and Pyrrolones as Modulators of GABA sub(A) Receptors

Targeting PDE10A in schizophrenia

Targeting PDE10A in schizophrenia

ChemInform Abstract: 5-(4-Hydroxy-6-methyl-2-oxo-2H-pyran-3-yl) -7-phenyl-2,3,6,7-tetrahydro-1,4-thiazepines as Compounds with High Affinity at the Benzodiazepine Binding Site on GABAA Receptors

ChemInform Abstract: 5‐(4‐Hydroxy‐6‐methyl‐2‐oxo‐2H‐pyran‐3‐yl) ‐7‐phenyl‐2,3,6,7‐tetrahydro‐1,4‐thiazepines as Compounds with High Affinity at the Benzodiazepine Binding Site on GABA A Receptors

1,5-Disubstituted Indazol-3-ols with Anti-Inflammatory Activity

ChemInform Abstract: Indazole-3-oles and Indazole-2-ones with Antiinflammatory Activity

ChemInform Abstract: 1,5-Disubstituted Indazol-3-ols with anti-Inflammatory Activity

Lost Earnings and Nonmedical Expenses of Pediatric Hospitalizations

Highly Potent, Selective, and Orally Active Phosphodiesterase 10A Inhibitors

48. Sertoli Leydig Cell Tumor Presenting With Elevated Adrenal Markers in an Adolescent

Discovery of Imidazo[1,5-a]pyrido[3,2-e]pyrazines as a New Class of Phosphodiesterase 10A Inhibitiors

Invasive Ductal Carcinoma in A 46,XY Partial Androgen Insensitivity Syndrome Patient on Hormone Therapy

Rope Swing Injuries Resulting in Vulvar Trauma

Novel triazines as potent and selective phosphodiesterase 10A inhibitors

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