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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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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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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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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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Conformational analysis of tripeptide Ac-Lys-Pro-Val-NH2, COOH-terminal sequence of alpha-MSH

Journal of pharmacy and pharmacology, 2001-07, Vol.53 (7), p.949-953

2001

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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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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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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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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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Synthesis and Pharmacological Evaluation of New Pyrazolidine-3,5-diones as AT1 Angiotensin II Receptor Antagonists

Journal of medicinal chemistry, 2000-07, Vol.43 (14), p.2685-2697

2000

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N-[2-(7-Methoxy-1-naphthyl)ethyl]acetamide, a potent melatonin analog

Acta crystallographica. Section C, Crystal structure communications, 1994-06, Vol.50 (6), p.907-910

1994

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Novel 2(3H)-Benzothiazolones as Highly Potent and Selective Sigma-1 Receptor Ligands

Medicinal chemistry research, 2005-01, Vol.14 (3), p.158-168

2005

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Synthesis and Structure-Activity Relationships of Novel Naphthalenic and Bioisosteric Related Amidic Derivatives as Melatonin Receptor Ligands

Journal of medicinal chemistry, 1994-09, Vol.37 (20), p.3231-3239

1994

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Lipid-lowering properties of 6-benzoyl-2(3H)-benzothiazolone and structurally related compounds

Journal of enzyme inhibition and medicinal chemistry, 2005-12, Vol.20 (6), p.525-532

2005

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BEXAROTENE-ACTIVATED RXR/LXR HETERODIMER IN LIVER MODULATES TRIGLYCERIDE METABOLISM BUT NOT CHOLESTEROL HOMEOSTASIS IN VIVO

ATHEROSCLEROSIS SUPPLEMENTS, 2008, Vol.9 (1), p.25-25

2008

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Enantiomeric resolution of new aromatase inhibitors by liquid chromatography on cellulose chiral stationary phases

Journal of separation science, 2005-03, Vol.28 (5), p.428-434

2005

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

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

2004

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AlCl3-DMF Reagent in the Friedel-Crafts Reaction. Application to the Acylation Reaction of 2(3H)-Benzothiazolones

Journal of organic chemistry, 1994-03, Vol.59 (6), p.1574-1576

1994

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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

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

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

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

Conformational analysis of tripeptide Ac-Lys-Pro-Val-NH2, COOH-terminal sequence of alpha-MSH

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

Pictet–Spengler heterocyclizations via microwave-assisted degradation of DMSO

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

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

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

Synthesis and Pharmacological Evaluation of New Pyrazolidine-3,5-diones as AT1 Angiotensin II Receptor Antagonists

N-[2-(7-Methoxy-1-naphthyl)ethyl]acetamide, a potent melatonin analog

Novel 2(3H)-Benzothiazolones as Highly Potent and Selective Sigma-1 Receptor Ligands

Synthesis and Structure-Activity Relationships of Novel Naphthalenic and Bioisosteric Related Amidic Derivatives as Melatonin Receptor Ligands

Lipid-lowering properties of 6-benzoyl-2(3H)-benzothiazolone and structurally related compounds

BEXAROTENE-ACTIVATED RXR/LXR HETERODIMER IN LIVER MODULATES TRIGLYCERIDE METABOLISM BUT NOT CHOLESTEROL HOMEOSTASIS IN VIVO

Enantiomeric resolution of new aromatase inhibitors by liquid chromatography on cellulose chiral stationary phases

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

AlCl3-DMF Reagent in the Friedel-Crafts Reaction. Application to the Acylation Reaction of 2(3H)-Benzothiazolones

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