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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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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 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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A calcineurin antifungal strategy with analogs of FK506

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

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 (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

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