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Comparison of capillary electrophoresis and reversed-phase liquid chromatography for determination of the enantiomeric purity of an M3 antagonist

Journal of Chromatography A, 2002-06, Vol.959 (1), p.299-308

2002

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Identification and initial structure-activity relationships of a novel non-peptide quinolone GnRH receptor antagonist

Bioorganic & medicinal chemistry letters, 1999-09, Vol.9 (17), p.2615-2620

1999

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Potent antagonists of gonadotropin releasing hormone receptors derived from quinolone-6-carboxamides

Bioorganic & medicinal chemistry letters, 2000-03, Vol.10 (5), p.443-447

2000

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Investigation of the 4-O-alkylamine substituent of non-peptide quinolone GnRH receptor antagonists

Bioorganic & medicinal chemistry letters, 1999-09, Vol.9 (17), p.2621-2624

1999

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Quinolones as gonadotropin releasing hormone (GnRH) antagonists: simultaneous optimization of the C(3)-aryl and C(6)-substituents

Bioorganic & medicinal chemistry letters, 2000-08, Vol.10 (15), p.1723-1727

2000

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Chromatographic separation of 3,4-difluorophenylacetic acid and its positional isomers using five different techniques

Journal of Chromatography A, 2000-01, Vol.866 (2), p.281-292

2000

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Broad spectrum antiprotozoal agents that inhibit histone deacetylase: Structure-activity relationships of apicidin. Part 1

Bioorganic & medicinal chemistry letters, 2001-01, Vol.11 (2), p.107-111

2001

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Acyclic structural variants of growth hormone secretagogue L-692,429

Bioorganic & medicinal chemistry letters, 1999-11, Vol.9 (22), p.3237-3242

1999

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Initial structure–activity relationship of a novel class of nonpeptidyl GnRH receptor antagonists: 2-arylindoles

Bioorganic & medicinal chemistry letters, 2001-02, Vol.11 (4), p.509-513

2001

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Broad spectrum antiprotozoal agents that inhibit histone deacetylase: Structure-activity relationships of apicidin. Part 2

Bioorganic & medicinal chemistry letters, 2001-01, Vol.11 (2), p.113-117

2001

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Chiral capillary electrophoretic analysis of the enantiomeric purity of a pharmaceutical compound using sulfated β-cyclodextrin

Journal of Chromatography A, 2000-04, Vol.875 (1), p.389-401

2000

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C32-O-imidazol-2-yl-methyl ether derivatives of the immunosuppressant ascomycin with improved therapeutic potential

Bioorganic & medicinal chemistry letters, 1998-08, Vol.8 (16), p.2253-2258

1998

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C32-O-phenalkyl ether derivatives of the immunosuppressant ascomycin: a tether length study

Bioorganic & medicinal chemistry letters, 1999-07, Vol.9 (14), p.2085-2088

1999

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Potent immunosuppressive C32-O-arylethyl ether derivatives of ascomycin with reduced toxicity

Bioorganic & medicinal chemistry letters, 1999-07, Vol.9 (14), p.2089-2094

1999

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Synthesis and SAR of 1,2- trans-(1-hydroxy-3-phenylprop-1-yl)cyclopentane carboxamide derivatives, a new class of sodium channel blockers

Bioorganic & medicinal chemistry letters, 2006-03, Vol.16 (5), p.1358-1361

2006

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SAR studies of novel 5-substituted 2-arylindoles as nonpeptidyl GnRH receptor antagonists

Bioorganic & medicinal chemistry letters, 2001-02, Vol.11 (4), p.515-517

2001

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2-(3,5-Dimethylphenyl)tryptamine Derivatives that Bind to the GnRH Receptor

Bioorganic & medicinal chemistry letters, 2001-04, Vol.11 (8), p.1073-1076

2001

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Heterocyclic Derivatives of 2-(3,5-Dimethylphenyl)tryptamine as GnRH Receptor Antagonists

Bioorganic & medicinal chemistry letters, 2001-04, Vol.11 (8), p.1077-1080

2001

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Synthesis of Nodulisporic Acid 2‘ ‘-Oxazoles and 2‘ ‘-Thiazoles

Organic letters, 2001-11, Vol.3 (23), p.3715-3718

2001

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Chemical modification of nodulisporic acid A: preliminary structure–activity relationships

Bioorganic & medicinal chemistry letters, 2000-10, Vol.10 (20), p.2371-2374

2000

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Development of an Indirect Reverse Phase Method for the Quality Assessment of an Acyl Halide

Journal of liquid chromatography & related technologies, 1998-02, Vol.21 (4), p.575-589

1998

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Discovery of a novel class of biphenyl pyrazole sodium channel blockers for treatment of neuropathic pain

Bioorganic & medicinal chemistry letters, 2010-12, Vol.20 (24), p.7479-7482

2010

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Thermal rearrangement of the immunosuppressant FK-506

Tetrahedron letters, 1990, Vol.31 (45), p.6477-6480

1990

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Human β 3-adrenergic receptor agonists containing 1,2,3-triazole-substituted benzenesulfonamides

Bioorganic & medicinal chemistry letters, 2000-09, Vol.10 (18), p.2111-2114

2000

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Substituted biaryl pyrazoles as sodium channel blockers

Bioorganic & medicinal chemistry letters, 2010-09, Vol.20 (18), p.5480-5483

2010

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Comparison of capillary electrophoresis and reversed-phase liquid chromatography for determination of the enantiomeric purity of an M3 antagonist

Identification and initial structure-activity relationships of a novel non-peptide quinolone GnRH receptor antagonist

Potent antagonists of gonadotropin releasing hormone receptors derived from quinolone-6-carboxamides

Investigation of the 4-O-alkylamine substituent of non-peptide quinolone GnRH receptor antagonists

Quinolones as gonadotropin releasing hormone (GnRH) antagonists: simultaneous optimization of the C(3)-aryl and C(6)-substituents

Chromatographic separation of 3,4-difluorophenylacetic acid and its positional isomers using five different techniques

Broad spectrum antiprotozoal agents that inhibit histone deacetylase: Structure-activity relationships of apicidin. Part 1

Acyclic structural variants of growth hormone secretagogue L-692,429

Initial structure–activity relationship of a novel class of nonpeptidyl GnRH receptor antagonists: 2-arylindoles

Broad spectrum antiprotozoal agents that inhibit histone deacetylase: Structure-activity relationships of apicidin. Part 2

Chiral capillary electrophoretic analysis of the enantiomeric purity of a pharmaceutical compound using sulfated β-cyclodextrin

C32-O-imidazol-2-yl-methyl ether derivatives of the immunosuppressant ascomycin with improved therapeutic potential

C32-O-phenalkyl ether derivatives of the immunosuppressant ascomycin: a tether length study

Potent immunosuppressive C32-O-arylethyl ether derivatives of ascomycin with reduced toxicity

Synthesis and SAR of 1,2- trans-(1-hydroxy-3-phenylprop-1-yl)cyclopentane carboxamide derivatives, a new class of sodium channel blockers

SAR studies of novel 5-substituted 2-arylindoles as nonpeptidyl GnRH receptor antagonists

2-(3,5-Dimethylphenyl)tryptamine Derivatives that Bind to the GnRH Receptor

Heterocyclic Derivatives of 2-(3,5-Dimethylphenyl)tryptamine as GnRH Receptor Antagonists

Synthesis of Nodulisporic Acid 2‘ ‘-Oxazoles and 2‘ ‘-Thiazoles

Chemical modification of nodulisporic acid A: preliminary structure–activity relationships

Development of an Indirect Reverse Phase Method for the Quality Assessment of an Acyl Halide

Discovery of a novel class of biphenyl pyrazole sodium channel blockers for treatment of neuropathic pain

Thermal rearrangement of the immunosuppressant FK-506

Human β 3-adrenergic receptor agonists containing 1,2,3-triazole-substituted benzenesulfonamides

Substituted biaryl pyrazoles as sodium channel blockers

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