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Structural basis for selective inhibition of cyclooxygenase-2 by anti-inflammatory agents

Nature (London), 1996-12, Vol.384 (6610), p.644-648

1996

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1,2-Diarylpyrroles as Potent and Selective Inhibitors of Cyclooxygenase-2

Journal of medicinal chemistry, 1997-05, Vol.40 (11), p.1619-1633

1997

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Lower Eyelid Hernia Repair for Palpebral Bags: A Comparative Study

Plastic and reconstructive surgery (1963), 1998-12, Vol.102 (7), p.2459-2465

1998

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Vitreoretinal findings similar to retinopathy of prematurity in infants with compound heterozygous protein S deficiency

Ophthalmology (Rochester, Minn.), 1999-08, Vol.106 (8), p.1525-1530

1999

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Penetrating ocular injury with a fetal scalp monitoring spiral electrode

American journal of ophthalmology, 1999-10, Vol.128 (4), p.526-528

1999

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Lasso procedure to revise overcorrection with radial keratotomy

American journal of ophthalmology, 1998-12, Vol.126 (6), p.825-827

1998

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Synthesis and Biological Evaluation of the 1,5-Diarylpyrazole Class of Cyclooxygenase-2 Inhibitors: Identification of 4-[5-(4-Methylphenyl)-3- (trifluoromethyl)-1H-pyrazol-1-yl]benzenesulfonamide (SC-58635, Celecoxib)

Journal of medicinal chemistry, 1997-04, Vol.40 (9), p.1347-1365

1997

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Structure-activity relationship studies on 1-[2-(4-Phenylphenoxy)ethyl]pyrrolidine (SC-22716), a potent inhibitor of leukotriene A(4) (LTA(4)) hydrolase

Journal of medicinal chemistry, 2000-02, Vol.43 (4), p.721-735

2000

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12(R)-Hydroxyeicosatetraenoic acid is a neutrophil chemoattractant in the cavine, lapine, murine and canine dermis

Prostaglandins, leukotrienes and essential fatty acids, 1989-08, Vol.37 (2), p.79-81

1989

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SC-41930 inhibits neutrophil infiltration of the cavine dermis induced by 12(R)-hydroxyeicosatetraenoic acid

Prostaglandins, leukotrienes and essential fatty acids, 1989-12, Vol.38 (3), p.169-172

1989

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Lyme Disease Associated with Unilateral Interstitial Keratitis

Cornea, 1999-01, Vol.18 (1), p.115-116

1999

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Second Generation Leukotriene B4 Receptor Antagonists Related to SC-41930: Heterocyclic Replacement of the Methyl Ketone Pharmacophore

Journal of medicinal chemistry, 1995-03, Vol.38 (6), p.858-868

1995

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Synthesis and biological evaluation of the 1,5-diarylpyrazole class of cyclooxygenase-2 inhibitors: identification of 4-[5-(4-methylphenyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl]benze nesulfonamide (SC-58635, celecoxib)

Journal of medicinal chemistry, 1997-04, Vol.40 (9), p.1347-1365

1997

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A practical enantioselective synthesis of 12-hydroxyeicosatetraenoic acids

Tetrahedron letters, 1988, Vol.29 (28), p.3459-3462

1988

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Synthesis of potent leukotriene A(4) hydrolase inhibitors. Identification of 3-[methyl[3-[4-(phenylmethyl)phenoxy]propyl]amino]propanoic acid

Journal of medicinal chemistry, 2002-08, Vol.45 (16), p.3482-3490

2002

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Pyrrolidine and piperidine analogues of SC-57461A as potent, orally active inhibitors of leukotriene A(4) hydrolase

Bioorganic & medicinal chemistry letters, 2002-12, Vol.12 (23), p.3383

2002

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Structural basis for selective inhibition of cyclooxygenase-2 by anti-inflammatory agents

Nature (London), 1997-02, Vol.385 (6616), p.555-555

1997

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Improved Procedure for the Reduction of N-Acyloxazolidinones

Synthetic communications, 1990-01, Vol.20 (2), p.307-312

1990

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ChemInform Abstract: A Practical Enantioselective Synthesis of 12‐Hydroxyeicosatetraenoic Acid (VII)

ChemInform, 1988-12, Vol.19 (52), p.no-no

1988

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ChemInform Abstract: Synthesis and Biological Evaluation of the 1,5-Diarylpyrazole Class of Cyclooxygenase-2 Inhibitors: Identification of 4-(5-(4-Methylphenyl)-3- (trifluoromethyl)-1H-pyrazol-1-yl)benzenesulfonamide (SC-58635, Celecoxib)

ChemInform, 1997-09, Vol.28 (36), p.no-no

1997

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ChemInform Abstract: 1,2-Diarylpyrroles as Potent and Selective Inhibitors of Cyclooxygenase-2

ChemInform, 1997-09, Vol.28 (39), p.no-no

1997

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ChemInform Abstract: Improved Procedure for the Reduction of N‐Acyloxazolidinones

ChemInform, 1990-07, Vol.21 (30), p.no-no

1990

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Immunotherapy against experimental canine visceral leishmaniasis with the saponin enriched-Leishmune® vaccine

Vaccine, 2007-08, Vol.25 (33), p.6176-6190

2007

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Development and characterization of a novel liquid crystalline system containing sodium alginate for incorporation of trans-resveratrol intended for treatment of buccal candidiasis

Pharmazie, 2020-05, Vol.75 (5), p.179-185

2020

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Should a Stoma Be Used After Intestinal Transplant

Gastroenterology clinics of North America, 2024-06, Vol.53 (2), p.299-308

2024

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Structural basis for selective inhibition of cyclooxygenase-2 by anti-inflammatory agents

1,2-Diarylpyrroles as Potent and Selective Inhibitors of Cyclooxygenase-2

Lower Eyelid Hernia Repair for Palpebral Bags: A Comparative Study

Vitreoretinal findings similar to retinopathy of prematurity in infants with compound heterozygous protein S deficiency

Penetrating ocular injury with a fetal scalp monitoring spiral electrode

Lasso procedure to revise overcorrection with radial keratotomy

Synthesis and Biological Evaluation of the 1,5-Diarylpyrazole Class of Cyclooxygenase-2 Inhibitors: Identification of 4-[5-(4-Methylphenyl)-3- (trifluoromethyl)-1H-pyrazol-1-yl]benzenesulfonamide (SC-58635, Celecoxib)

Structure-activity relationship studies on 1-[2-(4-Phenylphenoxy)ethyl]pyrrolidine (SC-22716), a potent inhibitor of leukotriene A(4) (LTA(4)) hydrolase

12(R)-Hydroxyeicosatetraenoic acid is a neutrophil chemoattractant in the cavine, lapine, murine and canine dermis

SC-41930 inhibits neutrophil infiltration of the cavine dermis induced by 12(R)-hydroxyeicosatetraenoic acid

Lyme Disease Associated with Unilateral Interstitial Keratitis

Second Generation Leukotriene B4 Receptor Antagonists Related to SC-41930: Heterocyclic Replacement of the Methyl Ketone Pharmacophore

Synthesis and biological evaluation of the 1,5-diarylpyrazole class of cyclooxygenase-2 inhibitors: identification of 4-[5-(4-methylphenyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl]benze nesulfonamide (SC-58635, celecoxib)

A practical enantioselective synthesis of 12-hydroxyeicosatetraenoic acids

Synthesis of potent leukotriene A(4) hydrolase inhibitors. Identification of 3-[methyl[3-[4-(phenylmethyl)phenoxy]propyl]amino]propanoic acid

Pyrrolidine and piperidine analogues of SC-57461A as potent, orally active inhibitors of leukotriene A(4) hydrolase

Structural basis for selective inhibition of cyclooxygenase-2 by anti-inflammatory agents

Improved Procedure for the Reduction of N-Acyloxazolidinones

ChemInform Abstract: A Practical Enantioselective Synthesis of 12‐Hydroxyeicosatetraenoic Acid (VII)

ChemInform Abstract: Synthesis and Biological Evaluation of the 1,5-Diarylpyrazole Class of Cyclooxygenase-2 Inhibitors: Identification of 4-(5-(4-Methylphenyl)-3- (trifluoromethyl)-1H-pyrazol-1-yl)benzenesulfonamide (SC-58635, Celecoxib)

ChemInform Abstract: 1,2-Diarylpyrroles as Potent and Selective Inhibitors of Cyclooxygenase-2

ChemInform Abstract: Improved Procedure for the Reduction of N‐Acyloxazolidinones

Immunotherapy against experimental canine visceral leishmaniasis with the saponin enriched-Leishmune® vaccine

Development and characterization of a novel liquid crystalline system containing sodium alginate for incorporation of trans-resveratrol intended for treatment of buccal candidiasis

Should a Stoma Be Used After Intestinal Transplant

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