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Three-Dimensional Quantitative Structure−Activity Relationships of Cyclo-oxygenase-2 (COX-2) Inhibitors: A Comparative Molecular Field Analysis

Journal of medicinal chemistry, 2001-09, Vol.44 (20), p.3223-3230

2001

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Determination of ionization constants of N-imidazole derivatives, aromatase inhibitors, using capillary electrophoresis and influence of substituents on pKa shifts

Journal of Chromatography A, 2004-04, Vol.1035 (1), p.131-136

2004

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Antioxidant activity of melatonin and a pinoline derivative on linoleate model system

Journal of pineal research, 2005-08, Vol.39 (1), p.27-33

2005

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2(3H)-benzoxazolone and bioisosters as "privileged scaffold" in the design of pharmacological probes

Current medicinal chemistry, 2005-01, Vol.12 (7), p.877

2005

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Rexinoid bexarotene modulates triglyceride but not cholesterol metabolism via gene-specific permissivity of the RXR/LXR heterodimer in the liver

Arteriosclerosis, thrombosis, and vascular biology, 2009-10, Vol.29 (10), p.1488

2009

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Novel naphthalenic ligands with high affinity for the melatonin receptor

Journal of medicinal chemistry, 1992-04, Vol.35 (8), p.1484-1486

1992

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Exposure to glycol ethers in a population of French men evaluated by measurement of urinary alkoxycarboxylic acids

International archives of occupational and environmental health, 2004-06, Vol.77 (5), p.368-372

2004

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Synthesis and Evaluation of Benzoxazolinonic Imidazoles and Derivatives as Non-steroidal Aromatase Inhibitors

Journal of enzyme inhibition and medicinal chemistry, 2004-04, Vol.19 (2), p.119-127

2004

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Chiral resolution of the enantiomers of new aromatase inhibitors by liquid chromatography on amylose stationary phases

Chromatographia, 2004-02, Vol.59 (3-4), p.181-188

2004

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The RXR agonist bexarotene improves cholesterol homeostasis and inhibits atherosclerosis progression in a mouse model of mixed dyslipidemia

Arteriosclerosis, thrombosis, and vascular biology, 2006-12, Vol.26 (12), p.2731

2006

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New radioligands for describing the molecular pharmacology of MT1 and MT2 melatonin receptors

International journal of molecular sciences, 2013-04, Vol.14 (5), p.8948-8962

2013

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Characterization of the melatoninergic MT3 binding site on the NRH:quinone oxidoreductase 2 enzyme

Biochemical pharmacology, 2005-12, Vol.71 (1-2), p.74-88

2005

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Synthesis of 6-Cycloalkyl-2(3H)-benzoxazolones and Benzoxathiazolones via 6-Tri-N-butyltin Intermediates

Synthetic communications, 2004-01, Vol.34 (14), p.2601-2609

2004

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Direct separation of the stereoisomers of methoxytetrahydronaphthalene derivatives, new agonist and antagonist ligands for melatonin receptors, by liquid chromatography on cellulose chiral stationary phases

Journal of Chromatography A, 2001-01, Vol.907 (1), p.101-113

2001

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Design, Synthesis and In Vitro Evaluation of Novel Benzo[b]thiophene Derivatives as Serotonin N-acetyltransferase (AANAT) Inhibitors

Journal of enzyme inhibition and medicinal chemistry, 2003-04, Vol.18 (2), p.119-125

2003

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Synthesis of 2(3H)-benzoxazolone and 2(3H)-benzothiazolone derivatives as potential beta-3-adrenergic receptor ligands (part 2)

Journal of heterocyclic chemistry, 2001-05, Vol.38 (3), p.633-639

2001

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Design, Synthesis and In Vitro Evaluation of Novel Derivatives as Serotonin N -Acetyltransferase Inhibitors

Journal of enzyme inhibition and medicinal chemistry, 2002-01, Vol.17 (6), p.409-414

2002

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Pictet–Spengler heterocyclizations via microwave-assisted degradation of DMSO

Tetrahedron letters, 2005-04, Vol.46 (14), p.2465-2468

2005

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Synthesis of 2(3H)-benzoxazolinone derivatives as potential beta-3-adrenergic receptor ligands

Journal of heterocyclic chemistry, 1999-09, Vol.36 (5), p.1241-1245

1999

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Investigations of new lead structures for the design of novel cyclooxygenase-2 inhibitors

European journal of medicinal chemistry, 2002-06, Vol.37 (6), p.461-468

2002

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Synthesis of 6‐Cycloalkyl‐2(3 H )‐benzoxazolones and Benzoxathiazolones via 6‐Tri‐N‐butyltin Intermediates

Synthetic communications, 2011-01, Vol.34 (14), p.2601-2609

2011

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Design and Synthesis of Naphthalenic Dimers as Selective MT1 Melatoninergic Ligands

Journal of medicinal chemistry, 2003-03, Vol.46 (7), p.1127-1129

2003

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Design and synthesis of 3-phenyl tetrahydronaphthalenic derivatives as new selective MT2 melatoninergic ligands

Bioorganic & medicinal chemistry, 2003-03, Vol.11 (5), p.753-759

2003

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Efficient and selective deprotection method for N-protected 2( 3H)-benzoxazolones and 2( 3H)-benzothiazolones

Tetrahedron, 2004-11, Vol.60 (45), p.10321-10324

2004

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Synthesis of Nitroindole Derivatives with High Affinity and Selectivity for Melatoninergic Binding Sites MT3

Journal of medicinal chemistry, 2002-04, Vol.45 (9), p.1853-1859

2002

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Three-Dimensional Quantitative Structure−Activity Relationships of Cyclo-oxygenase-2 (COX-2) Inhibitors: A Comparative Molecular Field Analysis

Determination of ionization constants of N-imidazole derivatives, aromatase inhibitors, using capillary electrophoresis and influence of substituents on pKa shifts

Antioxidant activity of melatonin and a pinoline derivative on linoleate model system

2(3H)-benzoxazolone and bioisosters as "privileged scaffold" in the design of pharmacological probes

Rexinoid bexarotene modulates triglyceride but not cholesterol metabolism via gene-specific permissivity of the RXR/LXR heterodimer in the liver

Novel naphthalenic ligands with high affinity for the melatonin receptor

Exposure to glycol ethers in a population of French men evaluated by measurement of urinary alkoxycarboxylic acids

Synthesis and Evaluation of Benzoxazolinonic Imidazoles and Derivatives as Non-steroidal Aromatase Inhibitors

Chiral resolution of the enantiomers of new aromatase inhibitors by liquid chromatography on amylose stationary phases

The RXR agonist bexarotene improves cholesterol homeostasis and inhibits atherosclerosis progression in a mouse model of mixed dyslipidemia

New radioligands for describing the molecular pharmacology of MT1 and MT2 melatonin receptors

Characterization of the melatoninergic MT3 binding site on the NRH:quinone oxidoreductase 2 enzyme

Synthesis of 6-Cycloalkyl-2(3H)-benzoxazolones and Benzoxathiazolones via 6-Tri-N-butyltin Intermediates

Direct separation of the stereoisomers of methoxytetrahydronaphthalene derivatives, new agonist and antagonist ligands for melatonin receptors, by liquid chromatography on cellulose chiral stationary phases

Design, Synthesis and In Vitro Evaluation of Novel Benzo[b]thiophene Derivatives as Serotonin N-acetyltransferase (AANAT) Inhibitors

Synthesis of 2(3H)-benzoxazolone and 2(3H)-benzothiazolone derivatives as potential beta-3-adrenergic receptor ligands (part 2)

Design, Synthesis and In Vitro Evaluation of Novel Derivatives as Serotonin N -Acetyltransferase Inhibitors

Pictet–Spengler heterocyclizations via microwave-assisted degradation of DMSO

Synthesis of 2(3H)-benzoxazolinone derivatives as potential beta-3-adrenergic receptor ligands

Investigations of new lead structures for the design of novel cyclooxygenase-2 inhibitors

Synthesis of 6‐Cycloalkyl‐2(3 H )‐benzoxazolones and Benzoxathiazolones via 6‐Tri‐N‐butyltin Intermediates

Design and Synthesis of Naphthalenic Dimers as Selective MT1 Melatoninergic Ligands

Design and synthesis of 3-phenyl tetrahydronaphthalenic derivatives as new selective MT2 melatoninergic ligands

Efficient and selective deprotection method for N-protected 2( 3H)-benzoxazolones and 2( 3H)-benzothiazolones

Synthesis of Nitroindole Derivatives with High Affinity and Selectivity for Melatoninergic Binding Sites MT3

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