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Ring-fused thiadiazines as core structures for the development of potent AMPA receptor potentiators

Current medicinal chemistry, 2010-10, Vol.17 (30), p.3575

2010

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A potent and selective NPY Y5 antagonist reduces food intake but not through blockade of the NPY Y5 receptor

International Journal of Obesity, 2004-04, Vol.28 (4), p.628-639

2004

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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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Synthesis and Biological Evaluation of Novel Naphthocarbazoles as Potential Anticancer Agents

Journal of medicinal chemistry, 2005-03, Vol.48 (5), p.1401-1413

2005

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Novel and Selective Partial Agonists of 5-HT3 Receptors. 2. Synthesis and Biological Evaluation of Piperazinopyridopyrrolopyrazines, Piperazinopyrroloquinoxalines, and Piperazinopyridopyrroloquinoxalines

Journal of medicinal chemistry, 1997-06, Vol.40 (12), p.1808-1819

1997

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Semisynthesis and Cytotoxicity of Styryl-Lactone Derivatives

Journal of natural products (Washington, D.C.), 1999-08, Vol.62 (8), p.1106-1109

1999

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3-Amino-3,4-dihydro-2H-1-benzopyran Derivatives as 5-HT1A Receptor Ligands and Potential Anxiolytic Agents. 2. Synthesis and Quantitative Structure−Activity Relationship Studies of Spiro[pyrrolidine- and piperidine-2,3‘(2‘H)-benzopyrans]

Journal of medicinal chemistry, 1996-10, Vol.39 (21), p.4285-4298

1996

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Novel antitumor artemisinin derivatives targeting G1 phase of the cell cycle

Bioorganic & medicinal chemistry letters, 2001-01, Vol.11 (1), p.5-8

2001

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Synthèse et étude de l'activité antidépressive d'aryl et hétéroaryl carboxamides de la benzylpipérazine

Annales pharmaceutiques françaises, 2000, Vol.58 (4), p.254-259

2000

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Synthesis of isoquinolines and tetrahydroisoquinolines as potential antitumour agents

Tetrahedron, 2001-09, Vol.57 (39), p.8297-8303

2001

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Substituted pyrido[3,2- b]oxazin-3(4 H)-ones: synthesis and evaluation of antinociceptive activity

Bioorganic & medicinal chemistry, 1998-02, Vol.6 (2), p.133-142

1998

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Novel Indole-2-carboxamide and Cycloalkeno[1,2-b]indole Derivatives. Structure−Activity Relationships for High Inhibition of Human LDL Peroxidation

Journal of medicinal chemistry, 1997-04, Vol.40 (8), p.1201-1210

1997

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6-Aminoalkyloxazolo[4,5- b]pyridin-2(3 H)-ones: Synthesis and Evaluation of Antinoceptive Activity

Bioorganic & medicinal chemistry, 1998-11, Vol.6 (11), p.1963-1973

1998

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Synthesis of Omeprazole Analogues and Evaluation of These as Potential Inhibitors of the Multidrug Efflux Pump NorA of Staphylococcus aureus

Antimicrobial Agents and Chemotherapy, 2007-03, Vol.51 (3), p.831-838

2007

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Synthesis and cytotoxicity of artemisinin derivatives containing cyanoarylmethyl group

European journal of medicinal chemistry, 2001-05, Vol.36 (5), p.469-479

2001

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Design, Synthesis, and Pharmacology of Novel 7-Substituted 3,4-Dihydro-2H-1,2,4-benzothiadiazine 1,1-Dioxides as Positive Allosteric Modulators of AMPA Receptors

Journal of medicinal chemistry, 2007-06, Vol.50 (13), p.3153-3157

2007

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Synthesis and evaluation of new 2-piperazinylbenzothiazoles with high 5-HT1A and 5-HT3 affinities

European journal of medicinal chemistry, 1995, Vol.30 (9), p.715-719

1995

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Isomers of substituted 3-benzo[b]furyl and 3-thienylaminobutyric acids as potent ligands of the GABA-B receptor: synthesis and preparative liquid chromatographic separation

Therapie, 1999-09, Vol.54 (5), p.651

1999

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Antitumor agents. Synthesis and biological evaluation of new compounds related to podophyllotoxin, containing the 2,3-dihydro-1,4-benzodioxin system

European journal of medicinal chemistry, 2001-04, Vol.36 (4), p.389-393

2001

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Synthesis and Structure−Activity Relationships of New Benzodioxinic Lactones as Potential Anticancer Drugs

Journal of medicinal chemistry, 2007-01, Vol.50 (2), p.294-307

2007

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New antagonist agents of neuropeptide y receptors

Química Nova, 2000-12, Vol.23 (6), p.737-741

2000

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N-Substituted Oxazolo[5,4-b]pyridin-2(1H)-ones: A New Class of Non-Opiate Antinociceptive Agents

Journal of medicinal chemistry, 1995-04, Vol.38 (8), p.1278-1286

1995

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Synthesis and structure–activity relationships of novel arylalkyl 4-benzyl piperazine derivatives as σ site selective ligands

European journal of medicinal chemistry, 2000, Vol.35 (1), p.107-121

2000

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Functional characterization of human neuropeptide Y receptor subtype five specific antagonists using a luciferase reporter gene assay

Cellular signalling, 2005-04, Vol.17 (4), p.489-496

2005

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Synthesis of New Aromatic Pyrrolo[2,1- c] [1,4]benzodiazepines and Pyrrolo[1,2- a] thieno[3,2- e] [1,4]diazepines as Anti-tumoral Agents

Journal of enzyme inhibition and medicinal chemistry, 2002-01, Vol.17 (6), p.403-407

2002

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Ring-fused thiadiazines as core structures for the development of potent AMPA receptor potentiators

A potent and selective NPY Y5 antagonist reduces food intake but not through blockade of the NPY Y5 receptor

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

Synthesis and Biological Evaluation of Novel Naphthocarbazoles as Potential Anticancer Agents

Novel and Selective Partial Agonists of 5-HT3 Receptors. 2. Synthesis and Biological Evaluation of Piperazinopyridopyrrolopyrazines, Piperazinopyrroloquinoxalines, and Piperazinopyridopyrroloquinoxalines

Semisynthesis and Cytotoxicity of Styryl-Lactone Derivatives

3-Amino-3,4-dihydro-2H-1-benzopyran Derivatives as 5-HT1A Receptor Ligands and Potential Anxiolytic Agents. 2. Synthesis and Quantitative Structure−Activity Relationship Studies of Spiro[pyrrolidine- and piperidine-2,3‘(2‘H)-benzopyrans]

Novel antitumor artemisinin derivatives targeting G1 phase of the cell cycle

Synthèse et étude de l'activité antidépressive d'aryl et hétéroaryl carboxamides de la benzylpipérazine

Synthesis of isoquinolines and tetrahydroisoquinolines as potential antitumour agents

Substituted pyrido[3,2- b]oxazin-3(4 H)-ones: synthesis and evaluation of antinociceptive activity

Novel Indole-2-carboxamide and Cycloalkeno[1,2-b]indole Derivatives. Structure−Activity Relationships for High Inhibition of Human LDL Peroxidation

6-Aminoalkyloxazolo[4,5- b]pyridin-2(3 H)-ones: Synthesis and Evaluation of Antinoceptive Activity

Synthesis of Omeprazole Analogues and Evaluation of These as Potential Inhibitors of the Multidrug Efflux Pump NorA of Staphylococcus aureus

Synthesis and cytotoxicity of artemisinin derivatives containing cyanoarylmethyl group

Design, Synthesis, and Pharmacology of Novel 7-Substituted 3,4-Dihydro-2H-1,2,4-benzothiadiazine 1,1-Dioxides as Positive Allosteric Modulators of AMPA Receptors

Synthesis and evaluation of new 2-piperazinylbenzothiazoles with high 5-HT1A and 5-HT3 affinities

Isomers of substituted 3-benzo[b]furyl and 3-thienylaminobutyric acids as potent ligands of the GABA-B receptor: synthesis and preparative liquid chromatographic separation

Antitumor agents. Synthesis and biological evaluation of new compounds related to podophyllotoxin, containing the 2,3-dihydro-1,4-benzodioxin system

Synthesis and Structure−Activity Relationships of New Benzodioxinic Lactones as Potential Anticancer Drugs

New antagonist agents of neuropeptide y receptors

N-Substituted Oxazolo[5,4-b]pyridin-2(1H)-ones: A New Class of Non-Opiate Antinociceptive Agents

Synthesis and structure–activity relationships of novel arylalkyl 4-benzyl piperazine derivatives as σ site selective ligands

Functional characterization of human neuropeptide Y receptor subtype five specific antagonists using a luciferase reporter gene assay

Synthesis of New Aromatic Pyrrolo[2,1- c] [1,4]benzodiazepines and Pyrrolo[1,2- a] thieno[3,2- e] [1,4]diazepines as Anti-tumoral Agents

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