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GSK1614343, a Novel Ghrelin Receptor Antagonist, Produces an Unexpected Increase of Food Intake and Body Weight in Rodents and Dogs

Neuroendocrinology, 2011-01, Vol.94 (2), p.158-168

2011

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Synthesis and Pharmacological Characterization of Novel Druglike Corticotropin-Releasing Factor 1 Antagonists

Journal of medicinal chemistry, 2008-12, Vol.51 (23), p.7370-7379

2008

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Synthesis and pharmacological characterization of constrained analogues of Vestipitant as in vitro potent and orally active NK1 receptor antagonists

Bioorganic & medicinal chemistry letters, 2010-01, Vol.20 (2), p.623-627

2010

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Dihydropyrrole[2,3-d]pyridine Derivatives as Novel Corticotropin-Releasing Factor-1 Antagonists: Mapping of the Receptor Binding Pocket by in Silico Docking Studies

Journal of medicinal chemistry, 2008-11, Vol.51 (22), p.7273-7286

2008

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Highly Diastereoselective Synthesis of 4- N-Methylformamidino Trinem (GV129606), a Potent Antibacterial Agent

Tetrahedron, 2000-07, Vol.56 (31), p.5649-5655

2000

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Benzoazepine derivative as potent antagonists of the glycine binding site associated to the NMDA receptor

Farmaco (Società chimica italiana : 1989), 2003-09, Vol.58 (9), p.723-738

2003

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Synthesis and pharmacological characterization of constrained analogues of Vestipitant as in vitro potent and orally active NK sub(1) receptor antagonists

Bioorganic & medicinal chemistry letters, 2010-01, Vol.20 (2), p.623-627

2010

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Synthesis and pharmacological characterization of constrained analogues of Vestipitant as in vitro potent and orally active NK 1 receptor antagonists

Bioorganic & medicinal chemistry letters, 2010, Vol.20 (2), p.623-627

2010

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Synthesis and pharmacological characterization of constrained analogues of Vestipitant as in vitro potent and orally active NK(1) receptor antagonists

Bioorganic & medicinal chemistry letters, 2010-01, Vol.20 (2), p.623-627

2010

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Selective Inhibitors of G2019S-LRRK2 Kinase Activity

Journal of medicinal chemistry, 2020-12, Vol.63 (23), p.14821-14839

2020

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A simultaneous outbreak of Serratia marcescens and Klebsiella pneumoniae in a neonatal intensive care unit

The Journal of hospital infection, 2005-12, Vol.61 (4), p.312-320

2005

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Understanding Factors Associated With Psychomotor Subtypes of Delirium in Older Inpatients With Dementia

Journal of the American Medical Directors Association, 2020-04, Vol.21 (4), p.486-492.e7

2020

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Computer‐aided photographic identification of Rosalia alpina (Coleoptera: Cerambycidae) applied to a mark‐recapture study

Insect conservation and diversity, 2017-01, Vol.10 (1), p.54-63

2017

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Enantiomerically pure tetrahydroquinoline derivatives as in vivo potent antagonists of the glycine binding site associated to the NMDA receptor

Bioorganic & medicinal chemistry letters, 2003-11, Vol.13 (21), p.3863-3866

2003

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Substituted tetraazaacenaphthylenes as potent CRF1 receptor antagonists for the treatment of depression and anxiety

Bioorganic & medicinal chemistry letters, 2005-08, Vol.15 (16), p.3713-3716

2005

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Azabicyclo[3.1.0]hexane-1-carbohydrazides as Potent and Selective GHSR1a Ligands Presenting a Specific in vivo Behavior

ChemMedChem, 2011-11, Vol.6 (11), p.1981-1985

2011

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Analysis of midwall shortening reveals high prevalence of left ventricular myocardial dysfunction in patients with diabetes mellitus: the DYDA study

European journal of preventive cardiology, 2012-10, Vol.19 (5), p.935-943

2012

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Synthesis and pharmacological characterisation of 2,4-Dicarboxy-pyrroles as selective non-Competitive mGluR1 antagonists

Bioorganic & medicinal chemistry, 2003-01, Vol.11 (2), p.171-183

2003

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Substituted Analogues of GV150526 as Potent Glycine Binding Site Antagonists in Animal Models of Cerebral Ischemia

Journal of medicinal chemistry, 1999-09, Vol.42 (18), p.3486-3493

1999

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2,4-Dicarboxy-pyrroles as selective non-Competitive mGluR1 antagonists: further characterization of 3,5-Dimethyl pyrrole-2,4-dicarboxylic acid 2-propyl ester 4-(1,2,2-Trimethyl-propyl) ester and structure–Activity relationships

Bioorganic & medicinal chemistry letters, 2003-07, Vol.13 (13), p.2113-2118

2003

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From pyrroles to pyrrolo[1,2- a]pyrazinones: A new class of mGluR1 antagonists

Bioorganic & medicinal chemistry letters, 2006-03, Vol.16 (5), p.1342-1345

2006

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Unusual concurrent detection by polymerase chain reaction of Bartonella henselae and parvovirus b19 in an immunocompetent child with erythema nodosum and hepatic granulomatous disease

Diagnostic microbiology and infectious disease, 2007-09, Vol.59 (1), p.81-84

2007

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Metabotropic glutamate receptors: potential therapeutic applications of recently disclosed new chemical entities

Expert opinion on therapeutic patents, 2004-11, Vol.14 (11), p.1593-1604

2004

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GSK1614343, a Novel Ghrelin Receptor Antagonist, Produces an Unexpected Increase of Food Intake and Body Weight in Rodents and Dogs

Cyclopenta[d]pyrimidines and Dihydropyrrolo[2,3-d]pyrimidines as Potent and Selective Corticotropin-Releasing Factor 1 Receptor Antagonists

Synthesis and Pharmacological Characterization of Novel Druglike Corticotropin-Releasing Factor 1 Antagonists

Synthesis and pharmacological characterization of constrained analogues of Vestipitant as in vitro potent and orally active NK1 receptor antagonists

Dihydropyrrole[2,3-d]pyridine Derivatives as Novel Corticotropin-Releasing Factor-1 Antagonists: Mapping of the Receptor Binding Pocket by in Silico Docking Studies

Highly Diastereoselective Synthesis of 4- N-Methylformamidino Trinem (GV129606), a Potent Antibacterial Agent

Benzoazepine derivative as potent antagonists of the glycine binding site associated to the NMDA receptor

Synthesis and pharmacological characterization of constrained analogues of Vestipitant as in vitro potent and orally active NK sub(1) receptor antagonists

Synthesis and pharmacological characterization of constrained analogues of Vestipitant as in vitro potent and orally active NK 1 receptor antagonists

Synthesis and pharmacological characterization of constrained analogues of Vestipitant as in vitro potent and orally active NK(1) receptor antagonists

Selective Inhibitors of G2019S-LRRK2 Kinase Activity

A simultaneous outbreak of Serratia marcescens and Klebsiella pneumoniae in a neonatal intensive care unit

Discovery Process and Characterization of Novel Carbohydrazide Derivatives as Potent and Selective GHSR1a Antagonists

Understanding Factors Associated With Psychomotor Subtypes of Delirium in Older Inpatients With Dementia

Computer‐aided photographic identification of Rosalia alpina (Coleoptera: Cerambycidae) applied to a mark‐recapture study

Enantiomerically pure tetrahydroquinoline derivatives as in vivo potent antagonists of the glycine binding site associated to the NMDA receptor

Substituted tetraazaacenaphthylenes as potent CRF1 receptor antagonists for the treatment of depression and anxiety

Azabicyclo[3.1.0]hexane-1-carbohydrazides as Potent and Selective GHSR1a Ligands Presenting a Specific in vivo Behavior

Analysis of midwall shortening reveals high prevalence of left ventricular myocardial dysfunction in patients with diabetes mellitus: the DYDA study

Synthesis and pharmacological characterisation of 2,4-Dicarboxy-pyrroles as selective non-Competitive mGluR1 antagonists

Substituted Analogues of GV150526 as Potent Glycine Binding Site Antagonists in Animal Models of Cerebral Ischemia

2,4-Dicarboxy-pyrroles as selective non-Competitive mGluR1 antagonists: further characterization of 3,5-Dimethyl pyrrole-2,4-dicarboxylic acid 2-propyl ester 4-(1,2,2-Trimethyl-propyl) ester and structure–Activity relationships

From pyrroles to pyrrolo[1,2- a]pyrazinones: A new class of mGluR1 antagonists

Unusual concurrent detection by polymerase chain reaction of Bartonella henselae and parvovirus b19 in an immunocompetent child with erythema nodosum and hepatic granulomatous disease

Metabotropic glutamate receptors: potential therapeutic applications of recently disclosed new chemical entities

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