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A new family of H3 receptor antagonists based on the natural product Conessine

Bioorganic & medicinal chemistry letters, 2008-02, Vol.18 (4), p.1490-1494

2008

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Discovery of 1-[3-(4-Bromo-2-methyl-2 H -pyrazol-3-yl)-4-methoxyphenyl]-3-(2,4-difluorophenyl)urea (Nelotanserin) and Related 5-Hydroxytryptamine 2A Inverse Agonists for the Treatment of Insomnia

Journal of medicinal chemistry, 2010-03, Vol.53 (5), p.1923-1936

2010

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Discovery and SAR of new benzazepines as potent and selective 5-HT 2C receptor agonists for the treatment of obesity

Bioorganic & medicinal chemistry letters, 2005-03, Vol.15 (5), p.1467-1470

2005

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Discovery of 1-[3-(4-Bromo-2-methyl-2H-pyrazol-3-yl)-4-methoxyphenyl]-3-(2,4-difluorophenyl)urea (Nelotanserin) and Related 5-Hydroxytryptamine2A Inverse Agonists for the Treatment of Insomnia

Journal of medicinal chemistry, 2010-03, Vol.53 (5), p.1923-1936

2010

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Resource ReviewsMastering the Instructional Design Process: A Systematic Approach, (2nd Ed.), by RothwellWilliam J.KazanasH. C.San Francisco, CA: Jossey-Bass, 1998. 425 pages, hard cover

Academy of Management learning & education, 2002-12, Vol.1 (2), p.220-221

Webb, Robert R.

2002

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Synthesis of 1-(aminooxy)-4-[(3-nitro-2-pyridyl)dithio]butane and 1-(aminooxy)-4-[(3-nitro-2-pyridyl)dithio]-2-butene, novel heterobifunctional crosslinking reagents

Bioconjugate chemistry, 1990-03, Vol.1 (2), p.96-99

1990

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Solubilized phenyl-pyrazole ureas as potent, selective 5-HT sub(2A) inverse-agonists and their application as antiplatelet agents

Bioorganic & medicinal chemistry letters, 2009-09, Vol.19 (18), p.5486-5489

2009

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Solubilized phenyl-pyrazole ureas as potent, selective 5-HT 2A inverse-agonists and their application as antiplatelet agents

Bioorganic & medicinal chemistry letters, 2009, Vol.19 (18), p.5486-5489

2009

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From Peptide to Non-Peptide. 2. The de Novo Design of Potent, Non-peptidal Inhibitors of Platelet Aggregation Based on a Benzodiazepinedione Scaffold

Journal of the American Chemical Society, 1994-06, Vol.116 (12), p.5077-5083

1994

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Causes and environmental implications of increased UV-B radiation

1, 2000

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A new family of H sub(3) receptor antagonists based on the natural product Conessine

Bioorganic & medicinal chemistry, 2008-02, Vol.18 (4), p.1490-1494

2008

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Reducing cannon plug connector pin selection time and errors through enhanced data presentation methods

Proceedings of the Human Factors and Ergonomics Society Annual Meeting, 1998, Vol.2, p.1286

1998

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Synthesis and antiviral activity of the nucleotide analog (S)-1-[3-hydroxy-2-(phosphonylmethoxy)propyl]cystosine

Journal of medicinal chemistry, 1989-07, Vol.32 (7), p.1457-1463

1989

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Discovery and SAR of new benzazepines as potent and selective 5-HT(2C) receptor agonists for the treatment of obesity

Bioorganic & medicinal chemistry letters, 2005-03, Vol.15 (5), p.1467-1470

2005

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Solubilized phenyl-pyrazole ureas as potent, selective 5-HT(2A) inverse-agonists and their application as antiplatelet agents

Bioorganic & medicinal chemistry letters, 2009-09, Vol.19 (18), p.5486-5489

2009

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Qualitative research in education: Focus and methods

1988

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A convenient synthesis of [formula omitted]-HPMPA

Tetrahedron letters, 1987, Vol.28 (42), p.4963-4964

1987

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Reducing Cannon Plug Connector Pin Selection Time and Errors Through Enhanced Data Presentation Methods

Proceedings of the Human Factors and Ergonomics Society Annual Meeting, 1998-10, Vol.42 (18), p.1286-1290

1998

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Synthesis of (S)- [formula omitted]1-(3-hydroxy-2-phosphonylmethoxy)propylcytosine, (S)-HPMPC

Tetrahedron letters, 1988, Vol.29 (43), p.5475-5478

1988

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Mastering the Instructional Design Process: A Systematic Approach

Academy of Management Learning & Education, 2002, Vol.1 (2), p.220-221

Webb, Robert R.

2002

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A new family of H3 receptor antagonists based on the natural product Conessine

Discovery and Structure−Activity Relationship of (1R)-8-Chloro-2,3,4,5-tetrahydro-1-methyl-1H-3-benzazepine (Lorcaserin), a Selective Serotonin 5-HT2C Receptor Agonist for the Treatment of Obesity

Discovery and Structure−Activity Relationship of 3-Methoxy-N-(3-(1-methyl-1H-pyrazol-5-yl)-4-(2-morpholinoethoxy)phenyl)benzamide (APD791): A Highly Selective 5-Hydroxytryptamine2A Receptor Inverse Agonist for the Treatment of Arterial Thrombosis

Discovery of 1-[3-(4-Bromo-2-methyl-2 H -pyrazol-3-yl)-4-methoxyphenyl]-3-(2,4-difluorophenyl)urea (Nelotanserin) and Related 5-Hydroxytryptamine 2A Inverse Agonists for the Treatment of Insomnia

Discovery and SAR of new benzazepines as potent and selective 5-HT 2C receptor agonists for the treatment of obesity

Discovery of 1-[3-(4-Bromo-2-methyl-2H-pyrazol-3-yl)-4-methoxyphenyl]-3-(2,4-difluorophenyl)urea (Nelotanserin) and Related 5-Hydroxytryptamine2A Inverse Agonists for the Treatment of Insomnia

Discovery and Structure−Activity Relationship of 3-Methoxy- N -(3-(1-methyl-1 H -pyrazol-5-yl)-4-(2-morpholinoethoxy)phenyl)benzamide (APD791): A Highly Selective 5-Hydroxytryptamine 2A Receptor Inverse Agonist for the Treatment of Arterial Thrombosis

Resource ReviewsMastering the Instructional Design Process: A Systematic Approach, (2nd Ed.), by RothwellWilliam J.KazanasH. C.San Francisco, CA: Jossey-Bass, 1998. 425 pages, hard cover

Synthesis of 1-(aminooxy)-4-[(3-nitro-2-pyridyl)dithio]butane and 1-(aminooxy)-4-[(3-nitro-2-pyridyl)dithio]-2-butene, novel heterobifunctional crosslinking reagents

Solubilized phenyl-pyrazole ureas as potent, selective 5-HT sub(2A) inverse-agonists and their application as antiplatelet agents

Solubilized phenyl-pyrazole ureas as potent, selective 5-HT 2A inverse-agonists and their application as antiplatelet agents

From Peptide to Non-Peptide. 2. The de Novo Design of Potent, Non-peptidal Inhibitors of Platelet Aggregation Based on a Benzodiazepinedione Scaffold

Discovery and Structure-Activity Relationship of (1R)-8-Chloro-2,3,4,5-tetrahydro-l-methyl-1H-3-benzazepine (Lorcaserin), a Selective Serotonin 5-HT2C Receptor Agonist for the Treatment of Obesity

Discovery and Structure−Activity Relationship of (1 R )-8-Chloro-2,3,4,5-tetrahydro-1-methyl-1 H -3-benzazepine (Lorcaserin), a Selective Serotonin 5-HT 2C Receptor Agonist for the Treatment of Obesity

Causes and environmental implications of increased UV-B radiation

A new family of H sub(3) receptor antagonists based on the natural product Conessine

Reducing cannon plug connector pin selection time and errors through enhanced data presentation methods

Synthesis and antiviral activity of the nucleotide analog (S)-1-[3-hydroxy-2-(phosphonylmethoxy)propyl]cystosine

Discovery and SAR of new benzazepines as potent and selective 5-HT(2C) receptor agonists for the treatment of obesity

Solubilized phenyl-pyrazole ureas as potent, selective 5-HT(2A) inverse-agonists and their application as antiplatelet agents

Qualitative research in education: Focus and methods

A convenient synthesis of [formula omitted]-HPMPA

Reducing Cannon Plug Connector Pin Selection Time and Errors Through Enhanced Data Presentation Methods

Synthesis of (S)- [formula omitted]1-(3-hydroxy-2-phosphonylmethoxy)propylcytosine, (S)-HPMPC

Mastering the Instructional Design Process: A Systematic Approach

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