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Synthesis and Activity of New Aryl- and Heteroaryl-Substituted Pyrazole Inhibitors of the Transforming Growth Factor-β Type I Receptor Kinase Domain

Journal of medicinal chemistry, 2003-09, Vol.46 (19), p.3953-3956

2003

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Synthesis and activity of new aryl- and heteroaryl-substituted 5,6-dihydro-4H-pyrrolo[1,2-b]pyrazole inhibitors of the transforming growth factor-β type I receptor kinase domain

Bioorganic & medicinal chemistry letters, 2004-07, Vol.14 (13), p.3581-3584

2004

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Kinetic Characterization of Novel Pyrazole TGF-β Receptor I Kinase Inhibitors and Their Blockade of the Epithelial−Mesenchymal Transition

Biochemistry (Easton), 2005-02, Vol.44 (7), p.2293-2304

2005

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Anthranilamide inhibitors of factor Xa

Bioorganic & medicinal chemistry letters, 2007-09, Vol.17 (17), p.4832-4836

2007

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N 2-Aroylanthranilamide Inhibitors of Human Factor Xa

Journal of medicinal chemistry, 2000-03, Vol.43 (5), p.873-882

2000

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Pharmacologic actions of the second-generation leukotriene B4 receptor antagonist LY293111: in vitro studies

The Journal of pharmacology and experimental therapeutics, 1999-01, Vol.288 (1), p.286

1999

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High-Affinity Aptamers Selectively Inhibit Human Nonpancreatic Secretory Phospholipase A2 (hnps-PLA2)

Journal of medicinal chemistry, 1998-03, Vol.41 (6), p.778-786

1998

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Development of a series of phenyltetrazole leukotriene D4(LTD4) receptor antagonists

Journal of medicinal chemistry, 1992-04, Vol.35 (7), p.1191-1200

1992

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1,2-Dibenzamidobenzene Inhibitors of Human Factor Xa

Journal of medicinal chemistry, 2000-03, Vol.43 (5), p.859-872

2000

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Leukotriene B4 (LTB4) Receptor Antagonists: A Series of (Hydroxyphenyl)pyrazoles

Journal of medicinal chemistry, 1994-07, Vol.37 (15), p.2411-2420

1994

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Leukotriene B4 receptor antagonists: the LY255283 series of hydroxyacetophenones

Journal of medicinal chemistry, 1992-05, Vol.35 (10), p.1818-1828

1992

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Pulmonary actions of LY255283, a leukotriene B4 receptor antagonist

European journal of pharmacology, 1992-11, Vol.223 (1), p.57-64

1992

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New stereospecific synthetic routes to trisubstituted olefins

Journal of the American Chemical Society, 1970-11, Vol.92 (22), p.6635-6636

1970

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Electronic structures of cephalosporins and penicillins. 11. Parabolic relationships between antibacterial activity of cephalosporins and .beta.-lactam reactivity predicted from molecular orbital calculations

Journal of the American Chemical Society, 1980-03, Vol.102 (6), p.1812-1814

1980

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N(2)-Aroylanthranilamide inhibitors of human factor Xa

Journal of medicinal chemistry, 2000-03, Vol.43 (5), p.873-882

2000

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Non-Amidine-Containing 1,2-Dibenzamidobenzene Inhibitors of Human Factor Xa with Potent Anticoagulant and Antithrombotic Activity

Journal of medicinal chemistry, 2000-06, Vol.43 (11), p.2087-2092

2000

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Synthesis and activity of new aryl- and heteroaryl-substituted 5,6-dihydro-4 H-pyrrolo[1,2- b]pyrazole inhibitors of the transforming growth factor-β type I receptor kinase domain

Bioorganic & medicinal chemistry letters, 2004, Vol.14 (13), p.3581-3584

2004

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Solution photolysis of camphor

Journal of the American Chemical Society, 1968-12, Vol.90 (25), p.7025-7030

1968

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OVID and SUPER: two overlap programs for drug design

Journal of computer-aided molecular design, 1991-12, Vol.5 (6), p.511-524

1991

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Convenient synthesis of 2,2-dimethylcyclobutanone

Journal of organic chemistry, 1969-09, Vol.34 (9), p.2782-2785

1969

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N2-Aroylanthranilamide Inhibitors of Human Factor Xa

Journal of medicinal chemistry, 2000-03, Vol.43 (5), p.873-882

2000

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High-Affinity Aptamers Selectively Inhibit Human Nonpancreatic Secretory Phospholipase A 2 (hnps-PLA 2 )

Journal of medicinal chemistry, 1998-03, Vol.41 (6), p.778-786

1998

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Common Structural Requirements for Peroxisome Proliferation by Tetrazole and Carboxylic Acid-Containing Compounds

Annals of the New York Academy of Sciences, 1996-12, Vol.804 (1), p.387-402

1996

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2-alkyl-4-ethyl-5-[6-methyl-6-(2H-tetrazol-5-yl)heptyloxy]phenol leukotriene B4 receptor antagonists

Bioorganic & medicinal chemistry letters, 1995-09, Vol.5 (17), p.1995-2000

1995

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Synthesis and Activity of New Aryl- and Heteroaryl-Substituted Pyrazole Inhibitors of the Transforming Growth Factor-β Type I Receptor Kinase Domain

Synthesis and activity of new aryl- and heteroaryl-substituted 5,6-dihydro-4H-pyrrolo[1,2-b]pyrazole inhibitors of the transforming growth factor-β type I receptor kinase domain

Kinetic Characterization of Novel Pyrazole TGF-β Receptor I Kinase Inhibitors and Their Blockade of the Epithelial−Mesenchymal Transition

Anthranilamide inhibitors of factor Xa

N 2-Aroylanthranilamide Inhibitors of Human Factor Xa

Pharmacologic actions of the second-generation leukotriene B4 receptor antagonist LY293111: in vitro studies

High-Affinity Aptamers Selectively Inhibit Human Nonpancreatic Secretory Phospholipase A2 (hnps-PLA2)

Development of a series of phenyltetrazole leukotriene D4(LTD4) receptor antagonists

1,2-Dibenzamidobenzene Inhibitors of Human Factor Xa

Leukotriene B4 (LTB4) Receptor Antagonists: A Series of (Hydroxyphenyl)pyrazoles

Leukotriene B4 receptor antagonists: the LY255283 series of hydroxyacetophenones

Pulmonary actions of LY255283, a leukotriene B4 receptor antagonist

New stereospecific synthetic routes to trisubstituted olefins

Electronic structures of cephalosporins and penicillins. 11. Parabolic relationships between antibacterial activity of cephalosporins and .beta.-lactam reactivity predicted from molecular orbital calculations

N(2)-Aroylanthranilamide inhibitors of human factor Xa

Non-Amidine-Containing 1,2-Dibenzamidobenzene Inhibitors of Human Factor Xa with Potent Anticoagulant and Antithrombotic Activity

Structure-Based Design of Potent, Amidine-Derived Inhibitors of Factor Xa: Evaluation of Selectivity, Anticoagulant Activity, and Antithrombotic Activity

Synthesis and activity of new aryl- and heteroaryl-substituted 5,6-dihydro-4 H-pyrrolo[1,2- b]pyrazole inhibitors of the transforming growth factor-β type I receptor kinase domain

Solution photolysis of camphor

OVID and SUPER: two overlap programs for drug design

Convenient synthesis of 2,2-dimethylcyclobutanone

N2-Aroylanthranilamide Inhibitors of Human Factor Xa

High-Affinity Aptamers Selectively Inhibit Human Nonpancreatic Secretory Phospholipase A 2 (hnps-PLA 2 )

Common Structural Requirements for Peroxisome Proliferation by Tetrazole and Carboxylic Acid-Containing Compounds

2-alkyl-4-ethyl-5-[6-methyl-6-(2H-tetrazol-5-yl)heptyloxy]phenol leukotriene B4 receptor antagonists

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