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Conformationally constrained farnesoid X receptor (FXR) agonists: Naphthoic acid-based analogs of GW 4064

Bioorganic & medicinal chemistry, 2008-08, Vol.18 (15), p.4339-4343

2008

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α1-Adrenoceptor agonists: The identification of novel α1A Subtype selective 2'-heteroaryl-2-(phenoxymethyl)imidazolines

Bioorganic & medicinal chemistry letters, 2002-02, Vol.12 (3), p.471-475

2002

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Conformationally constrained farnesoid X receptor (FXR) agonists: Heteroaryl replacements of the naphthalene

Bioorganic & medicinal chemistry letters, 2011-02, Vol.21 (4), p.1206-1213

2011

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FXR agonist activity of conformationally constrained analogs of GW 4064

Bioorganic & medicinal chemistry letters, 2009-08, Vol.19 (16), p.4733-4739

2009

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Conformationally constrained farnesoid X receptor (FXR) agonists: Alternative replacements of the stilbene

Bioorganic & medicinal chemistry letters, 2011-10, Vol.21 (20), p.6154-6160

2011

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α1-Adrenoceptor activation: A comparison of 4-(anilinomethyl)imidazoles and 4-(phenoxymethyl)imidazoles to related 2-imidazolines

Bioorganic & medicinal chemistry letters, 2002-12, Vol.12 (23), p.3449-3452

2002

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Synthesis of 3-alkyl naphthalenes as novel estrogen receptor ligands

Bioorganic & medicinal chemistry, 2008-09, Vol.18 (18), p.5075-5077

2008

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2-(anilinomethyl)imidazolines as α1 adrenergic receptor agonists : α1a subtype selective 2'-heteroaryl compounds

Bioorganic & medicinal chemistry letters, 2003-03, Vol.13 (6), p.1183-1186

2003

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2-(Anilinomethyl)imidazolines as α1A adrenergic receptor agonists: 2'-heteroaryl and 2'-oxime ether series

Bioorganic & medicinal chemistry letters, 2002-02, Vol.12 (4), p.575-579

2002

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2-(Anilinomethyl)imidazolines as α1 Adrenergic Receptor Agonists: the Discovery of α1 a Subtype Selective 2‘-Alkylsulfonyl-Substituted Analogues

Journal of medicinal chemistry, 2002-05, Vol.45 (11), p.2229-2239

2002

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Analogues of the potential antipsychotic agent 1192U90: amide modifications

Bioorganic & medicinal chemistry, 1998-06, Vol.6 (6), p.811-823

1998

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α 1-Adrenoceptor activation: A comparison of 4-(Anilinomethyl)imidazoles and 4-(Phenoxymethyl)imidazoles to related 2-imidazolines

Bioorganic & medicinal chemistry letters, 2002, Vol.12 (23), p.3449-3452

2002

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α 1-Adrenoceptor Agonists: The Identification of Novel α 1A Subtype Selective 2′-Heteroaryl-2-(phenoxymethyl)imidazolines

Bioorganic & medicinal chemistry letters, 2002, Vol.12 (3), p.471-475

2002

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ChemInform Abstract: 2‐(Anilinomethyl)imidazolines as α 1α Adrenergic Receptor Agonists: 2′‐Heteroaryl and 2′‐Oxime Ether Series

ChemInform, 2002-05, Vol.33 (21)

Navas III, Frank

2002

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ChemInform Abstract: 2-(Anilinomethyl)imidazolines as α1α Adrenergic Receptor Agonists: 2′-Heteroaryl and 2′-Oxime Ether Series

ChemInform, 2002-05, Vol.33 (21), p.no-no

2002

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2‐(Anilinomethyl)imidazolines as α 1 Adrenergic Receptor Agonists: α 1a Subtype Selective 2′‐Heteroaryl Compounds

ChemInform, 2003-07, Vol.34 (30)

2003

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2-(Anilinomethyl)imidazolines as α1 Adrenergic Receptor Agonists: α1a Subtype Selective 2′-Heteroaryl Compounds

ChemInform, 2003-07, Vol.34 (30), p.no-no

2003

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Cyclic Benzamides as Mixed Dopamine D2/Serotonin 5-HT2 Receptor Antagonists: Potential Atypical Antipsychotic Agents

Journal of medicinal chemistry, 1994-08, Vol.37 (16), p.2552-2563

1994

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Synthesis and Evaluation of Heterocyclic Carboxamides as Potential Antipsychotic Agents

Journal of medicinal chemistry, 1996-11, Vol.39 (24), p.4692-4703

1996

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Structure−Activity Relationships of a Series of Substituted Benzamides: Potent D2/5-HT2 Antagonists and 5-HT1a Agonists as Neuroleptic Agents

Journal of medicinal chemistry, 1996-03, Vol.39 (5), p.1172-1188

1996

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Conformationally constrained farnesoid X receptor (FXR) agonists: Naphthoic acid-based analogs of GW 4064

α1-Adrenoceptor agonists: The identification of novel α1A Subtype selective 2'-heteroaryl-2-(phenoxymethyl)imidazolines

Conformationally constrained farnesoid X receptor (FXR) agonists: Heteroaryl replacements of the naphthalene

FXR agonist activity of conformationally constrained analogs of GW 4064

Conformationally constrained farnesoid X receptor (FXR) agonists: Alternative replacements of the stilbene

α1-Adrenoceptor activation: A comparison of 4-(anilinomethyl)imidazoles and 4-(phenoxymethyl)imidazoles to related 2-imidazolines

Synthesis of 3-alkyl naphthalenes as novel estrogen receptor ligands

2-(anilinomethyl)imidazolines as α1 adrenergic receptor agonists : α1a subtype selective 2'-heteroaryl compounds

2-(Anilinomethyl)imidazolines as α1A adrenergic receptor agonists: 2'-heteroaryl and 2'-oxime ether series

2-(Anilinomethyl)imidazolines as α1 Adrenergic Receptor Agonists: the Discovery of α1 a Subtype Selective 2‘-Alkylsulfonyl-Substituted Analogues

Analogues of the potential antipsychotic agent 1192U90: amide modifications

α 1-Adrenoceptor activation: A comparison of 4-(Anilinomethyl)imidazoles and 4-(Phenoxymethyl)imidazoles to related 2-imidazolines

α 1-Adrenoceptor Agonists: The Identification of Novel α 1A Subtype Selective 2′-Heteroaryl-2-(phenoxymethyl)imidazolines

ChemInform Abstract: 2‐(Anilinomethyl)imidazolines as α 1α Adrenergic Receptor Agonists: 2′‐Heteroaryl and 2′‐Oxime Ether Series

ChemInform Abstract: 2-(Anilinomethyl)imidazolines as α1α Adrenergic Receptor Agonists: 2′-Heteroaryl and 2′-Oxime Ether Series

2‐(Anilinomethyl)imidazolines as α 1 Adrenergic Receptor Agonists: α 1a Subtype Selective 2′‐Heteroaryl Compounds

2-(Anilinomethyl)imidazolines as α1 Adrenergic Receptor Agonists: α1a Subtype Selective 2′-Heteroaryl Compounds

Cyclic Benzamides as Mixed Dopamine D2/Serotonin 5-HT2 Receptor Antagonists: Potential Atypical Antipsychotic Agents

Synthesis and Evaluation of Heterocyclic Carboxamides as Potential Antipsychotic Agents

Structure−Activity Relationships of a Series of Substituted Benzamides: Potent D2/5-HT2 Antagonists and 5-HT1a Agonists as Neuroleptic Agents

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