Design, synthesis and biological evaluation of novel 1,3-diarylpyrazoles as cyclooxygenase inhibitors, antiplatelet and anticancer agents (original) (raw)

3-(2-Methoxytetrahydrofuran-2-yl)pyrazoles: a novel class of potent, selective cyclooxygenase-2 (COX-2) inhibitors

David Schwalb

Bioorganic & Medicinal Chemistry Letters, 2004

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Synthesis and Cyclooxygenase-2 (COX-2) Inhibiting Properties of 1,5- Diarylpyrazoles Possessing N-Substitution on the Sulfonamide (-SO2NH2) Moiety †

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Letters in Drug Design & Discovery, 2005

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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)

John Talley

Journal of Medicinal Chemistry, 1997

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Synthesis and SAR/3D-QSAR studies on the COX-2 inhibitory activity of 1,5-diarylpyrazoles to validate the modified pharmacophore

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European Journal of Medicinal Chemistry, 2005

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Synthesis of Fused Sulfonamide (1,1-Dioxoisothiazole)substituted 1,5-Diarylpyrazoles as Cyclooxygenase Inhibitors

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ChemInform, 2005

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Synthesis of new pyrazoles and pyrozolo [3,4-b] pyridines as anti-inflammatory agents by inhibition of COX-2 enzyme

shimaa Alhamaky

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Synthesis, anti-inflammatory, antiplatelet and in silico evaluations of (E)-3-(3-(2, 3-dihydro-3-methyl-2-oxo-3H-benzoxazole-6-yl)-1-phenyl-1H-pyrazole-4-yl) …

yesim ozkan

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3,4-diarylpyrazoles: Potent and selective inhibitors of cyclooxygenase-2

Steven Kramer

Bioorganic & Medicinal Chemistry Letters, 1997

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Synthesis and Biologic Evaluation of Substituted 5-methyl-2-phenyl-1H-pyrazol-3(2H)-one Derivatives as Selective COX-2 Inhibitors: Molecular Docking Study

YOGESH V . USHIR

CBDD, 2014

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Synthesis and biological evaluation of a new class of acyl derivatives of 3-amino-1-phenyl-4,5-dihydro-1H-pyrazol-5-one as potential dual cyclooxygenase (COX-1 and COX-2) and human lipoxygenase (5-LOX) inhibitors

Paolo Bernardi

Il Farmaco, 2005

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Design and synthesis of novel 2-phenyl-5-(1,3-diphenyl-1H-pyrazol-4-yl)-1,3,4-oxadiazoles as selective COX-2 inhibitors with potent anti-inflammatory activity

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European Journal of Medicinal Chemistry, 2014

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Synthesis, cyclooxygenase inhibition, anti-inflammatory evaluation and ulcerogenic liability of novel triarylpyrazoline derivatives as selective COX-2 inhibitors

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Synthesis, Biological Activity, and Molecular Modeling Studies of Pyrazole and Triazole Derivatives as Selective COX-2 Inhibitors

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Synthesis and Cyclooxygenase-2 Inhibiting Property of 1,5-Diarylpyrazoles with Substituted Benzenesulfonamide Moiety as Pharmacophore: Preparation of Sodium Salt for Injectable Formulation†

Rao Mamidi

Journal of Medicinal Chemistry, 2003

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Synthesis of 4-alkyl-1,2-diphenyl-3,5-dioxopyrazolidines possessing aryl methylsulfonyl and sulfonamide pharmacophores for evaluation as selective cyclooxygenase-2 (COX-2) inhibitors

Edward E Knaus

Journal of Heterocyclic Chemistry, 2002

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Methanesulfonamide group at position-4 of the C-5-phenyl ring of 1,5-diarylpyrazole affords a potent class of cyclooxygenase-2 (COX-2) inhibitors

Seshagiri Casturi

Bioorganic & Medicinal Chemistry Letters, 2004

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Synthesis of 1-P-SULF Am Ylphen YL-3 Trifluoromethylpyrazoles Class of CYCLOOXYGENASE-2 Inhibitors

HASSAN ALBAR

Heterocyclic Communications, 2003

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Synthesis, biological evaluation, and docking analysis of a novel family of 1-methyl-1H-pyrrole-2,5-diones as highly potent and selective cyclooxygenase-2 (COX-2) inhibitors

Jelena Penjišević

Bioorganic & Medicinal Chemistry Letters, 2014

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Synthesis and biological evaluation of 2,3-diarylpyrazines and quinoxalines as selective COX2 inhibitors

Pramod Hegde

Bioorganic & Medicinal Chemistry, 2004

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Synthesis, biological evaluation, and docking studies of novel heterocyclic diaryl compounds as selective COX-2 inhibitors

Beatrice Severino

Bioorganic & Medicinal Chemistry, 2010

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Synthesis and anti-inflammatory activity of some new thiadiazole linked pyrazole benzene sulphonamides as cyclooxygenase inhibitors

Rahmat Ali

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Synthesis and anti-inflammatory evaluation of new 1,3,5-triaryl-4,5- dihydro-1H-pyrazole derivatives possessing an aminosulphonyl pharmacophore

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Design, synthesis, and biological evaluation of substituted hydrazone and pyrazole derivatives as selective COX2 inhibitors: Molecular docking study

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Bioorganic & Medicinal Chemistry, 2011

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Synthesis, biological evaluation, and docking studies of 3-(substituted)-aryl-5-(9-methyl-3-carbazole)-1H-2-pyrazolines as potent anti-inflammatory and antioxidant agents

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Bioorganic & Medicinal Chemistry Letters, 2012

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2,3-Diarylpyran-4-ones: a new series of selective cyclooxygenase-2 inhibitors

Shin Chung

Bioorganic & Medicinal Chemistry Letters, 2004

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Novel Anti-inflammatory Agents Based on Pyrazole Based Dimeric Compounds; Design, Synthesis, Docking and in Vivo Activity

Ved Singh

Chemical & Pharmaceutical Bulletin, 2010

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Synthesis of novel 3,5-diaryl pyrazole derivatives using combinatorial chemistry as inhibitors of tyrosinase as well as potent anticancer, anti-inflammatory agents

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Bioorganic & Medicinal Chemistry, 2010

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Design and Synthesis of Benzimidazole Analogs Endowed with Oxadiazole as Selective COX-2 Inhibitor

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Synthesis and anti-inflammatory evaluation of new substituted 1-(3-chlorophenyl)-3-(4-methoxyphenyl)-1H-pyrazole derivatives

Nagy Khalifa

PubMed, 2012

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Cyclooxygenase-2 inhibitors. 1, 5-diarylpyrrol-3-acetic esters with enhanced inhibitory activity toward cyclooxygenase-2 and improved cyclooxygenase-2/ …

Fabrizio Manetti

Journal of medicinal …, 2007

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