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Three-Dimensional Quantitative Structure−Activity Relationship of Melatonin Receptor Ligands: A Comparative Molecular Field Analysis Study

Journal of medicinal chemistry, 1997-02, Vol.40 (5), p.739-748

1997

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Arylcarbamate Derivatives of 1-Piperidineethanol as Potent Ligands for 5-HT4 Receptors

Journal of medicinal chemistry, 1997-05, Vol.40 (11), p.1755-1761

1997

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Structural analysis of 5-HT3 receptor antagonists: synthesis and pharmacological activity of various aromatic esters or amides derived from tropane and 1,2,6-trisubstituted piperidine

European journal of medicinal chemistry, 1993, Vol.28 (11), p.869-880

1993

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Design and Synthesis of New Naphthalenic Derivatives as Ligands for 2-[125I]Iodomelatonin Binding Sites

Journal of medicinal chemistry, 1995-06, Vol.38 (12), p.2050-2060

1995

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New Esters of 4-Amino-5-chloro-2-methoxybenzoic Acid as Potent Agonists and Antagonists for 5-HT4 Receptors

Journal of medicinal chemistry, 1997-02, Vol.40 (4), p.608-621

1997

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Synthesis of 2-Amido-2,3-dihydro-1H-phenalene Derivatives as New Conformationally Restricted Ligands for Melatonin Receptors

Journal of medicinal chemistry, 1996-08, Vol.39 (16), p.3089-3095

1996

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Synthesis and pharmacological activity of a macrocyclic benzamide

Bioorganic & medicinal chemistry letters, 1995-04, Vol.5 (8), p.795-798

1995

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Serotoninergic properties of new conformationally restricted benzamides

European journal of medicinal chemistry, 1996, Vol.31 (3), p.231-239

1996

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Design of a potent 5-HT4 receptor agonist with nanomolar affinity

Bioorganic & medicinal chemistry letters, 1994-06, Vol.4 (12), p.1433-1436

1994

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Structure-activity relationships for substrates and inhibitors of pineal 5-hydroxytryptamine- N-acetyltransferase: preliminary studies

European journal of pharmacology, 1996-06, Vol.307 (2), p.133-140

1996

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Synthesis of quinazoline-2,4-dione and naphthalimide derivatives as new 5-HT3 receptor antagonists

European journal of medicinal chemistry, 1994, Vol.29 (12), p.925-940

1994

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Synthesis of new derivatives of 8-OH-DPAT: Influence of substitution on the aromatic ring on the pharmacological profile

Bioorganic & medicinal chemistry letters, 1993-10, Vol.3 (10), p.2035-2038

1993

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Derivatives of naphthalimide: new potent conformationally restricted antagonists of 5-HT3 receptors

Bioorganic & medicinal chemistry letters, 1992-07, Vol.2 (7), p.691-694

1992

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N-chloromethyl quinuclidinium derivatives : a new class of irreversible ligands for 5-HT3 receptors

Bioorganic & medicinal chemistry letters, 1994, Vol.4 (7), p.945-948

1994

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(-)-5-methyl-8-hydroxy-(di-n-propylamino)tetralin a new 5-HT1A receptor antagonist

European journal of medicinal chemistry, 1998-06, Vol.33 (6), p.437-444

1998

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Design and synthesis of new naphthalemic derivatives as ligands for 2-[125I]iodomelatonin binding sites

Journal of medicinal chemistry, 1995, Vol.38 (12), p.2050-2060

1995

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Structural analysis of 5-HT 3 receptor antagonists: synthesis and pharmacological activity of various aromatic esters or amides derived from tropane and 1,2,6-trisubstituted piperidine

European journal of medicinal chemistry, 1993, Vol.28 (11), p.869-880

1993

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Structural analysis by the comparative molecular field analysis method of the affinity of β-adrenoceptor blocking agents for 5-HT1A and 5-HT1B receptors

European journal of pharmacology. Molecular pharmacology section, 1993-01, Vol.244 (1), p.77-87

1993

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ChemInform Abstract: Serotoninergic Properties of New Conformationally Restricted Benzamides

ChemInform, 1996-07, Vol.27 (27), p.no-no

1996

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Environmental Growth Conditions of Trichoderma spp. Affects Indole Acetic Acid Derivatives, Volatile Organic Compounds, and Plant Growth Promotion

Frontiers in plant science, 2017-02, Vol.8, p.102-102

2017

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ChemInform Abstract: (‐)‐5‐Methyl‐8‐hydroxy‐(di‐n‐propylamino)tetralin: A New 5‐HT 1A Receptor Antagonist

ChemInform, 1999-01, Vol.30 (2)

1999

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The Major Portal of Entry of Koi Herpesvirus in Cyprinus carpio Is the Skin

Journal of Virology, 2009-04, Vol.83 (7), p.2819-2830

2009

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A dehydrin-dehydrin interaction: the case of SK3 from Opuntia streptacantha

Frontiers in plant science, 2014-10, Vol.5, p.520-520

2014

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ChemInform Abstract: (-)-5-Methyl-8-hydroxy-(di-n-propylamino)tetralin: A New 5-HT1A Receptor Antagonist

ChemInform, 1999-01, Vol.30 (2), p.no-no

1999

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ChemInform Abstract: Synthesis of Quinazoline-2,4-dione and Naphthalimide Derivatives as New 5-HT3 Receptor Antagonists

ChemInform, 1995-05, Vol.26 (21), p.no-no

1995

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Three-Dimensional Quantitative Structure−Activity Relationship of Melatonin Receptor Ligands: A Comparative Molecular Field Analysis Study

Arylcarbamate Derivatives of 1-Piperidineethanol as Potent Ligands for 5-HT4 Receptors

Structural analysis of 5-HT3 receptor antagonists: synthesis and pharmacological activity of various aromatic esters or amides derived from tropane and 1,2,6-trisubstituted piperidine

Design and Synthesis of New Naphthalenic Derivatives as Ligands for 2-[125I]Iodomelatonin Binding Sites

New Esters of 4-Amino-5-chloro-2-methoxybenzoic Acid as Potent Agonists and Antagonists for 5-HT4 Receptors

Synthesis of 2-Amido-2,3-dihydro-1H-phenalene Derivatives as New Conformationally Restricted Ligands for Melatonin Receptors

Synthesis and pharmacological activity of a macrocyclic benzamide

Serotoninergic properties of new conformationally restricted benzamides

Design of a potent 5-HT4 receptor agonist with nanomolar affinity

Structure-activity relationships for substrates and inhibitors of pineal 5-hydroxytryptamine- N-acetyltransferase: preliminary studies

Synthesis of quinazoline-2,4-dione and naphthalimide derivatives as new 5-HT3 receptor antagonists

Synthesis of new derivatives of 8-OH-DPAT: Influence of substitution on the aromatic ring on the pharmacological profile

Derivatives of naphthalimide: new potent conformationally restricted antagonists of 5-HT3 receptors

N-chloromethyl quinuclidinium derivatives : a new class of irreversible ligands for 5-HT3 receptors

(-)-5-methyl-8-hydroxy-(di-n-propylamino)tetralin a new 5-HT1A receptor antagonist

Design and synthesis of new naphthalemic derivatives as ligands for 2-[125I]iodomelatonin binding sites

Structural analysis of 5-HT 3 receptor antagonists: synthesis and pharmacological activity of various aromatic esters or amides derived from tropane and 1,2,6-trisubstituted piperidine

Structural analysis by the comparative molecular field analysis method of the affinity of β-adrenoceptor blocking agents for 5-HT1A and 5-HT1B receptors

ChemInform Abstract: Serotoninergic Properties of New Conformationally Restricted Benzamides

Environmental Growth Conditions of Trichoderma spp. Affects Indole Acetic Acid Derivatives, Volatile Organic Compounds, and Plant Growth Promotion

ChemInform Abstract: (‐)‐5‐Methyl‐8‐hydroxy‐(di‐n‐propylamino)tetralin: A New 5‐HT 1A Receptor Antagonist

The Major Portal of Entry of Koi Herpesvirus in Cyprinus carpio Is the Skin

A dehydrin-dehydrin interaction: the case of SK3 from Opuntia streptacantha

ChemInform Abstract: (-)-5-Methyl-8-hydroxy-(di-n-propylamino)tetralin: A New 5-HT1A Receptor Antagonist

ChemInform Abstract: Synthesis of Quinazoline-2,4-dione and Naphthalimide Derivatives as New 5-HT3 Receptor Antagonists

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