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Estimation of Contaminant Loads from the Sacramento-San Joaquin River Delta to San Francisco Bay

Water environment research, 2015-04, Vol.87 (4), p.334-346

2015

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Modeling the G-protein-coupled neuropeptide Y Y1 receptor agonist and antagonist binding sites

Protein engineering, 1997-02, Vol.10 (2), p.109-117

1997

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A Concise Synthesis of Atipamezole

Synthesis (Stuttgart), 1995-02, Vol.1995 (2), p.139-140

1995

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Facile access to the ABC ring system of the taxane diterpenes via anionic oxy-Cope rearrangements

Tetrahedron, 1995-03, Vol.51 (12), p.3455-3482

1995

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Design and synthesis of novel alpha(1)(a) adrenoceptor-selective antagonists. 1. Structure-activity relationship in dihydropyrimidinones

Journal of medicinal chemistry, 1999-11, Vol.42 (23), p.4764-4777

1999

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The α1-adrenergic receptor that mediates smooth muscle contraction in human prostate has the pharmacological properties of the cloned human α1c subtype

Molecular pharmacology, 1994, Vol.45 (4), p.703-708

1994

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Synthesis and structure-activity relationship of fluoro analogues of 8-{2-[4-(4-methoxyphenyl)piperazin-1yl]ethyl}-8-azaspiro[4.5]decane-7,9-dione as selective alpha(1d)-adrenergic receptor antagonists

Journal of medicinal chemistry, 2005-04, Vol.48 (8), p.3076-3079

2005

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Identification of a dihydropyridine as a potent alpha1a adrenoceptor-selective antagonist that inhibits phenylephrine-induced contraction of the human prostate

Journal of medicinal chemistry, 1998-07, Vol.41 (14), p.2643-2650

1998

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Cloning of the human homologue of the GABA transporter GAT-3 and identification of a novel inhibitor with selectivity for this site

Receptors & channels, 1994, Vol.2 (3), p.207

1994

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Design and synthesis of novel dihydropyridine alpha-1A antagonists

Bioorganic & medicinal chemistry letters, 1999-10, Vol.9 (19), p.2843-2848

1999

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Analogs of UK 14,304 as α2-adrenoceptor agonists. Twist and agent polarity as design elements

Bioorganic & medicinal chemistry letters, 1994-02, Vol.4 (3), p.459-462

1994

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Design and synthesis of novel alpha(1)(a) adrenoceptor-selective antagonists. 2. Approaches to eliminate opioid agonist metabolites via modification of linker and 4-methoxycarbonyl-4-phenylpiperidine moiety

Journal of medicinal chemistry, 1999-11, Vol.42 (23), p.4778-4793

1999

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Design, synthesis and SAR of a series of 2-substituted 4-amino-quinazoline neuropeptide Y Y5 receptor antagonists

Bioorganic & medicinal chemistry letters, 2000-06, Vol.10 (11), p.1175-1179

2000

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Design, Synthesis and Evaluation of Substituted Triarylnipecotic Acid Derivatives as GABA Uptake Inhibitors: Identification of a Ligand with Moderate Affinity and Selectivity for the Cloned Human GABA Transporter GAT-3

Journal of medicinal chemistry, 1994-07, Vol.37 (15), p.2334-2342

1994

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Localization of the alpha 1A-Adrenoceptor in the Human Prostate

The Journal of urology, 1995-12, Vol.154 (6), p.2096-2099

1995

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Design and synthesis of novel alpha(1)(a) adrenoceptor-selective antagonists. 3. Approaches to eliminate opioid agonist metabolites by using substituted phenylpiperazine side chains

Journal of medicinal chemistry, 1999-11, Vol.42 (23), p.4794-4803

1999

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Design and synthesis of novel alpha(1)(a) adrenoceptor-selective antagonists. 4. Structure-activity relationship in the dihydropyrimidine series

Journal of medicinal chemistry, 1999-11, Vol.42 (23), p.4804-4813

1999

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A double protection strategy for the synthesis of 3,5-disubstituted dihydropyridines

Tetrahedron letters, 1998-07, Vol.39 (30), p.5293-5296

1998

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2-amino-2-oxazolines as subtype selective alpha(2) adrenoceptor agonists

Journal of medicinal chemistry, 2000-05, Vol.43 (9), p.1699-1704

2000

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Studies on the ocular hypotensive effects of prostaglandin F2 alpha ester prodrugs and receptor selective prostaglandin analogs

Journal of ocular pharmacology, 1994, Vol.10 (1), p.177-193

1994

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Phenylacetamides as selective α-1A adrenergic receptor antagonists

Bioorganic & medicinal chemistry letters, 2000-08, Vol.10 (15), p.1621-1624

2000

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On the bioactive conformation of the gaba uptake inhibitor SK&F 89976-A

Bioorganic & medicinal chemistry letters, 1996-07, Vol.6 (13), p.1535-1540

1996

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Phenylacetamides as selective alpha-1A adrenergic receptor antagonists

Bioorganic & medicinal chemistry letters, 2000-08, Vol.10 (15), p.1621-1624

2000

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Ethyl (tributylstannyl)acetate: A versatile reagent for the carboethoxymethylation of functionalized pyridines

Tetrahedron letters, 1994-02, Vol.35 (7), p.989-992

1994

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Corneal and Conjunctival/Scleral Penetration of p-Aminoclonidine, AGN 190342, and Clonidine in Rabbit Eyes

Current eye research, 1990, Vol.9 (11), p.1051-1059

1990

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Estimation of Contaminant Loads from the Sacramento-San Joaquin River Delta to San Francisco Bay

Modeling the G-protein-coupled neuropeptide Y Y1 receptor agonist and antagonist binding sites

A Concise Synthesis of Atipamezole

Facile access to the ABC ring system of the taxane diterpenes via anionic oxy-Cope rearrangements

Design and synthesis of novel alpha(1)(a) adrenoceptor-selective antagonists. 1. Structure-activity relationship in dihydropyrimidinones

The α1-adrenergic receptor that mediates smooth muscle contraction in human prostate has the pharmacological properties of the cloned human α1c subtype

Synthesis and structure-activity relationship of fluoro analogues of 8-{2-[4-(4-methoxyphenyl)piperazin-1yl]ethyl}-8-azaspiro[4.5]decane-7,9-dione as selective alpha(1d)-adrenergic receptor antagonists

Identification of a dihydropyridine as a potent alpha1a adrenoceptor-selective antagonist that inhibits phenylephrine-induced contraction of the human prostate

Cloning of the human homologue of the GABA transporter GAT-3 and identification of a novel inhibitor with selectivity for this site

Design and synthesis of novel dihydropyridine alpha-1A antagonists

Analogs of UK 14,304 as α2-adrenoceptor agonists. Twist and agent polarity as design elements

Design and synthesis of novel alpha(1)(a) adrenoceptor-selective antagonists. 2. Approaches to eliminate opioid agonist metabolites via modification of linker and 4-methoxycarbonyl-4-phenylpiperidine moiety

Design, synthesis and SAR of a series of 2-substituted 4-amino-quinazoline neuropeptide Y Y5 receptor antagonists

Design, Synthesis and Evaluation of Substituted Triarylnipecotic Acid Derivatives as GABA Uptake Inhibitors: Identification of a Ligand with Moderate Affinity and Selectivity for the Cloned Human GABA Transporter GAT-3

Localization of the alpha 1A-Adrenoceptor in the Human Prostate

Design and synthesis of novel alpha(1)(a) adrenoceptor-selective antagonists. 3. Approaches to eliminate opioid agonist metabolites by using substituted phenylpiperazine side chains

Design and synthesis of novel alpha(1)(a) adrenoceptor-selective antagonists. 4. Structure-activity relationship in the dihydropyrimidine series

A double protection strategy for the synthesis of 3,5-disubstituted dihydropyridines

2-amino-2-oxazolines as subtype selective alpha(2) adrenoceptor agonists

Studies on the ocular hypotensive effects of prostaglandin F2 alpha ester prodrugs and receptor selective prostaglandin analogs

Phenylacetamides as selective α-1A adrenergic receptor antagonists

On the bioactive conformation of the gaba uptake inhibitor SK&F 89976-A

Phenylacetamides as selective alpha-1A adrenergic receptor antagonists

Ethyl (tributylstannyl)acetate: A versatile reagent for the carboethoxymethylation of functionalized pyridines

Corneal and Conjunctival/Scleral Penetration of p-Aminoclonidine, AGN 190342, and Clonidine in Rabbit Eyes

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