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Discovery of Disubstituted Cyclohexanes as a New Class of CC Chemokine Receptor 2 Antagonists

Journal of medicinal chemistry, 2008-02, Vol.51 (4), p.721-724

2008

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Benzimidazoles as benzamide replacements within cyclohexane-based CC chemokine receptor 2 (CCR2) antagonists

Bioorganic & medicinal chemistry letters, 2012-10, Vol.22 (19), p.6181-6184

2012

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γ-Lactams as glycinamide replacements in cyclohexane-based CC chemokine receptor 2 (CCR2) antagonists

Bioorganic & medicinal chemistry letters, 2010-04, Vol.20 (8), p.2425-2430

2010

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Novel sulfone-containing di- and trisubstituted cyclohexanes as potent CC chemokine receptor 2 (CCR2) antagonists

Bioorganic & medicinal chemistry letters, 2009-07, Vol.19 (13), p.3418-3422

2009

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Design, Synthesis, and Evaluation of Benzothiadiazepine Hydroxamates as Selective Tumor Necrosis Factor-α Converting Enzyme Inhibitors

Journal of medicinal chemistry, 2003-05, Vol.46 (10), p.1811-1823

2003

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Design, Synthesis, and Structure−Activity Relationships of Macrocyclic Hydroxamic Acids That Inhibit Tumor Necrosis Factor α Release in Vitro and in Vivo

Journal of medicinal chemistry, 2001-08, Vol.44 (16), p.2636-2660

2001

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Corannulene. A convenient new synthesis

Journal of the American Chemical Society, 1991-08, Vol.113 (18), p.7082-7084

1991

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Potent and selective aggrecanase inhibitors containing cyclic P1 substituents

Bioorganic & medicinal chemistry letters, 2003-04, Vol.13 (7), p.1297-1300

2003

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Preparation and Structure−Activity Relationship of Novel P1/P1‘-Substituted Cyclic Urea-Based Human Immunodeficiency Virus Type-1 Protease Inhibitors

Journal of medicinal chemistry, 1996-05, Vol.39 (11), p.2156-2169

1996

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Macrocyclic Amino Carboxylates as Selective MMP-8 Inhibitors

Journal of medicinal chemistry, 1998-05, Vol.41 (11), p.1749-1751

1998

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Sultam Hydroxamates as Novel Matrix Metalloproteinase Inhibitors

Journal of medicinal chemistry, 2004-06, Vol.47 (12), p.2981-2983

2004

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Corannulene. A Three-Step Synthesis1

Journal of the American Chemical Society, 1997-11, Vol.119 (45), p.10963-10968

1997

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g-Lactams as glycinamide replacements in cyclohexane-based CC chemokine receptor 2 (CCR2) antagonists

Bioorganic & medicinal chemistry letters, 2010-04, Vol.20 (8), p.2425-2430

2010

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Macrocyclic hydroxamate inhibitors of matrix metalloproteinases and TNF-α production

Bioorganic & medicinal chemistry letters, 1999-05, Vol.9 (9), p.1279-1284

1999

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Corannulene. A Three-Step Synthesis 1

Journal of the American Chemical Society, 1997-11, Vol.119 (45), p.10963-10968

1997

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Design, synthesis, and structure-activity relationships of macrocyclic hydroxamic acids that inhibit tumor necrosis factor a release in vitro and in vivo

Journal of medicinal chemistry, 2001, Vol.44 (16), p.2636-2660

2001

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Potent carboxylate inhibitors of stromelysin containing P2′ piperazic acids and P1′ biaryl moeities

Bioorganic & medicinal chemistry letters, 1997-07, Vol.7 (13), p.1757-1762

1997

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Synthetic and mechanistic studies of aromatic compounds at high temperatures: A new synthesis of corannulene

Meyer, Dayton T

1991

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Total Energy Intake is Decreased by an Internet-Delivered Physical Activity Behavior Change Program: 2833 Board #184 June 4 2:00 PM - 3:30 PM

Medicine and science in sports and exercise, 2010-05, Vol.42 (5), p.766

2010

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Analyses of rumen fluid from "sudden death", lactic acidotic and healthy cattle fed high concentrate ration

Journal of animal science, 1975-11, Vol.41 (5), p.1249

1975

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Analyses of Rumen Fluid from “Sudden Death,” Lactic Acidotic and Healthy Cattle Fed High Concentrate Ration1

Journal of animal science, 1975-11, Vol.41 (5), p.1249-1255

1975

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Discovery of Disubstituted Cyclohexanes as a New Class of CC Chemokine Receptor 2 Antagonists

Benzimidazoles as benzamide replacements within cyclohexane-based CC chemokine receptor 2 (CCR2) antagonists

γ-Lactams as glycinamide replacements in cyclohexane-based CC chemokine receptor 2 (CCR2) antagonists

Novel sulfone-containing di- and trisubstituted cyclohexanes as potent CC chemokine receptor 2 (CCR2) antagonists

Design, Synthesis, and Evaluation of Benzothiadiazepine Hydroxamates as Selective Tumor Necrosis Factor-α Converting Enzyme Inhibitors

Design, Synthesis, and Structure−Activity Relationships of Macrocyclic Hydroxamic Acids That Inhibit Tumor Necrosis Factor α Release in Vitro and in Vivo

Corannulene. A convenient new synthesis

Potent and selective aggrecanase inhibitors containing cyclic P1 substituents

Preparation and Structure−Activity Relationship of Novel P1/P1‘-Substituted Cyclic Urea-Based Human Immunodeficiency Virus Type-1 Protease Inhibitors

Macrocyclic Amino Carboxylates as Selective MMP-8 Inhibitors

Sultam Hydroxamates as Novel Matrix Metalloproteinase Inhibitors

Corannulene. A Three-Step Synthesis1

g-Lactams as glycinamide replacements in cyclohexane-based CC chemokine receptor 2 (CCR2) antagonists

Macrocyclic hydroxamate inhibitors of matrix metalloproteinases and TNF-α production

Corannulene. A Three-Step Synthesis 1

Design, synthesis, and structure-activity relationships of macrocyclic hydroxamic acids that inhibit tumor necrosis factor a release in vitro and in vivo

Potent carboxylate inhibitors of stromelysin containing P2′ piperazic acids and P1′ biaryl moeities

Synthetic and mechanistic studies of aromatic compounds at high temperatures: A new synthesis of corannulene

Total Energy Intake is Decreased by an Internet-Delivered Physical Activity Behavior Change Program: 2833 Board #184 June 4 2:00 PM - 3:30 PM

Analyses of rumen fluid from "sudden death", lactic acidotic and healthy cattle fed high concentrate ration

Analyses of Rumen Fluid from “Sudden Death,” Lactic Acidotic and Healthy Cattle Fed High Concentrate Ration1

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