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A calcineurin antifungal strategy with analogs of FK506

Bioorganic & medicinal chemistry letters, 2017-06, Vol.27 (11), p.2465-2471

2017

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Discovery and SAR of new benzazepines as potent and selective 5-HT2C receptor agonists for the treatment of obesity

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

2005

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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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Design, synthesis and in vitro evaluation of potent, novel, small molecule inhibitors of plasminogen activator inhibitor-1

Bioorganic & medicinal chemistry letters, 2002-04, Vol.12 (7), p.1063-1066

2002

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Solubilized phenyl-pyrazole ureas as potent, selective 5-HT2A 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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Synthesis of a tetramethyl analog of teleocidin

Journal of organic chemistry, 1991-07, Vol.56 (15), p.4706-4713

1991

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Alkaloid synthesis via intramolecular ene reactions. 1. Application to (.+-.)-crinane

Journal of the American Chemical Society, 1981-06, Vol.103 (11), p.3173-3177

1981

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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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Mono-N-alkylation of anthranilamides via quinazolinones. An efficient synthesis of G5598, a benzodiazepine dione gpIIbIIIa antagonist

Tetrahedron letters, 1994-04, Vol.35 (14), p.2113-2116

1994

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A new family of H 3 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-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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Alkaloid synthesis via intramolecular ene reaction. 2. Application to dl-mesembrine and dl-dihydromaritidine

Journal of organic chemistry, 1982-03, Vol.47 (7), p.1302-1309

1982

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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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Lewis acid catalyzed cyclocondensations of formaldehyde with activated dienes. A direct route to pyranosidal pentoses

Journal of organic chemistry, 1984-06, Vol.49 (11), p.1955-1958

1984

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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 calcineurin antifungal strategy with analogs of FK506

Discovery and SAR of new benzazepines as potent and selective 5-HT2C receptor agonists for the treatment of obesity

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

Design, synthesis and in vitro evaluation of potent, novel, small molecule inhibitors of plasminogen activator inhibitor-1

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

Solubilized phenyl-pyrazole ureas as potent, selective 5-HT2A inverse-agonists and their application as antiplatelet agents

Synthesis of a tetramethyl analog of teleocidin

Alkaloid synthesis via intramolecular ene reactions. 1. Application to (.+-.)-crinane

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

Mono-N-alkylation of anthranilamides via quinazolinones. An efficient synthesis of G5598, a benzodiazepine dione gpIIbIIIa antagonist

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

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

Alkaloid synthesis via intramolecular ene reaction. 2. Application to dl-mesembrine and dl-dihydromaritidine

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

Lewis acid catalyzed cyclocondensations of formaldehyde with activated dienes. A direct route to pyranosidal pentoses

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

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