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Safer anti-inflammatory therapy through dual COX-2/5-LOX inhibitors: A structure-based approach

European journal of pharmaceutical sciences, 2018-08, Vol.121, p.356-381

2018

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Substrate-selective Inhibition of Cyclooxygeanse-2 by Fenamic Acid Derivatives Is Dependent on Peroxide Tone

The Journal of biological chemistry, 2016-07, Vol.291 (29), p.15069-15081

2016

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Synthesis, anti-inflammatory, analgesic, COX-1/2 inhibitory activities and molecular docking studies of substituted 2-mercapto-4(3H)-quinazolinones

European journal of medicinal chemistry, 2016-10, Vol.121, p.410-421

2016

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Screening of chalcone analogs with anti-depressant, anti-inflammatory, analgesic, and COX-2-inhibiting effects

Bioorganic & medicinal chemistry letters, 2020-06, Vol.30 (11), p.127173, Article 127173

2020

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Design, synthesis, modeling studies and biological evaluation of thiazolidine derivatives containing pyrazole core as potential anti-diabetic PPAR-γ agonists and anti-inflammatory COX-2 selective inhibitors

Bioorganic chemistry, 2019-02, Vol.82, p.86-99

2019

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Synthesis, molecular docking and evaluation of novel sulfonyl hydrazones as anticancer agents and COX-2 inhibitors

Molecular diversity, 2020-08, Vol.24 (3), p.673-689

2020

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Characterization of spirostanol glycosides and furostanol glycosides from anemarrhenae rhizoma as dual targeted inhibitors of 5-lipoxygenase and Cyclooxygenase-2 by employing a combination of affinity ultrafiltration and HPLC/MS

Phytomedicine (Stuttgart), 2020-10, Vol.77, p.153284-153284, Article 153284

2020

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Pleiotropic mechanisms facilitated by resveratrol and its metabolites

Biochemical journal, 2010-07, Vol.429 (2), p.273-282

2010

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Inhibition of cyclooxygenase by blocking the reducing cosubstrate at the peroxidase site: Discovery of galangin as a novel cyclooxygenase inhibitor

European journal of pharmacology, 2021-05, Vol.899, p.174036, Article 174036

2021

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Molecular Mechanisms in the Selectivity of Nonsteroidal Anti-Inflammatory Drugs

Biochemistry (Easton), 2018-02, Vol.57 (7), p.1236-1248

2018

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A hybrid platform featuring nanomagnetic ligand fishing for discovering COX-2 selective inhibitors from aerial part of Saussurea laniceps Hand.-Mazz

Journal of ethnopharmacology, 2021-05, Vol.271, p.113849, Article 113849

2021

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Design, synthesis, and biological evaluation of substituted hydrazone and pyrazole derivatives as selective COX-2 inhibitors: Molecular docking study

Bioorganic & medicinal chemistry, 2011-06, Vol.19 (11), p.3416-3424

2011

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Synthesis of novel hybrids of pyrazole and coumarin as dual inhibitors of COX-2 and 5-LOX

Bioorganic & medicinal chemistry letters, 2017-08, Vol.27 (16), p.3653-3660

2017

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Fluorescent indomethacin-dansyl conjugates utilize the membrane-binding domain of cyclooxygenase-2 to block the opening to the active site

The Journal of biological chemistry, 2019-05, Vol.294 (22), p.8690-8698

2019

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Synthesis of new compounds bearing methyl sulfonyl pharmacophore as selective COX‐2 inhibitor

Journal of molecular recognition, 2023-07, Vol.36 (7), p.e3025-n/a

2023

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New 1,3,4-Oxadiazole Derivatives of Pyridothiazine-1,1-Dioxide with Anti-Inflammatory Activity

International journal of molecular sciences, 2020-11, Vol.21 (23), p.9122

2020

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Crystal structure of rofecoxib bound to human cyclooxygenase-2

Acta crystallographica. Section F, Structural biology communications, 2016-10, Vol.72 (10), p.772-776

2016

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Synthesis, molecular docking and anti-inflammatory screening of novel quinoline incorporated pyrazole derivatives using the Pfitzinger reaction II

Bioorganic chemistry, 2015-02, Vol.58, p.104-116

2015

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Automatic evaluation of cyclooxygenase 2 inhibition induced by metal-based anticancer compounds

Journal of inorganic biochemistry, 2021-05, Vol.218, p.111399-111399, Article 111399

2021

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Synthesis of Hydroxybenzofuranyl-pyrazolyl and Hydroxyphenyl-pyrazolyl Chalcones and Their Corresponding Pyrazoline Derivatives as COX Inhibitors, Anti-inflammatory and Gastroprotective Agents

Chemical and Pharmaceutical Bulletin, 2020/08/01, Vol.68(8), pp.742-752

2020

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Dual-target inhibitors based on COX-2: a review from medicinal chemistry perspectives

Future medicinal chemistry, 2023-12, Vol.15 (23), p.2209-2233

2023

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Novel diphenylthiazole derivatives with multi-target mechanism: Synthesis, docking study, anticancer and anti-inflammatory activities

Bioorganic chemistry, 2017-12, Vol.75, p.127-138

2017

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Fatty Acid Binding to the Allosteric Subunit of Cyclooxygenase-2 Relieves a Tonic Inhibition of the Catalytic Subunit

The Journal of biological chemistry, 2016-12, Vol.291 (49), p.25641-25655

2016

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Synthesis, biological evaluation, molecular docking and theoretical evaluation of ADMET properties of nepodin and chrysophanol derivatives as potential cyclooxygenase (COX-1, COX-2) inhibitors

European journal of medicinal chemistry, 2014-06, Vol.80, p.47-56

2014

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Human Cyclooxygenase-2 Is a Sequence Homodimer That Functions as a Conformational Heterodimer

The Journal of biological chemistry, 2011-05, Vol.286 (21), p.19035-19046

2011

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Safer anti-inflammatory therapy through dual COX-2/5-LOX inhibitors: A structure-based approach

Substrate-selective Inhibition of Cyclooxygeanse-2 by Fenamic Acid Derivatives Is Dependent on Peroxide Tone

Synthesis, anti-inflammatory, analgesic, COX-1/2 inhibitory activities and molecular docking studies of substituted 2-mercapto-4(3H)-quinazolinones

Screening of chalcone analogs with anti-depressant, anti-inflammatory, analgesic, and COX-2-inhibiting effects

Design, synthesis, modeling studies and biological evaluation of thiazolidine derivatives containing pyrazole core as potential anti-diabetic PPAR-γ agonists and anti-inflammatory COX-2 selective inhibitors

Synthesis, molecular docking and evaluation of novel sulfonyl hydrazones as anticancer agents and COX-2 inhibitors

Characterization of spirostanol glycosides and furostanol glycosides from anemarrhenae rhizoma as dual targeted inhibitors of 5-lipoxygenase and Cyclooxygenase-2 by employing a combination of affinity ultrafiltration and HPLC/MS

Pleiotropic mechanisms facilitated by resveratrol and its metabolites

Inhibition of cyclooxygenase by blocking the reducing cosubstrate at the peroxidase site: Discovery of galangin as a novel cyclooxygenase inhibitor

Molecular Mechanisms in the Selectivity of Nonsteroidal Anti-Inflammatory Drugs

A hybrid platform featuring nanomagnetic ligand fishing for discovering COX-2 selective inhibitors from aerial part of Saussurea laniceps Hand.-Mazz

Design, synthesis, and biological evaluation of substituted hydrazone and pyrazole derivatives as selective COX-2 inhibitors: Molecular docking study

Synthesis of novel hybrids of pyrazole and coumarin as dual inhibitors of COX-2 and 5-LOX

Fluorescent indomethacin-dansyl conjugates utilize the membrane-binding domain of cyclooxygenase-2 to block the opening to the active site

Synthesis of new compounds bearing methyl sulfonyl pharmacophore as selective COX‐2 inhibitor

New 1,3,4-Oxadiazole Derivatives of Pyridothiazine-1,1-Dioxide with Anti-Inflammatory Activity

Crystal structure of rofecoxib bound to human cyclooxygenase-2

Synthesis, molecular docking and anti-inflammatory screening of novel quinoline incorporated pyrazole derivatives using the Pfitzinger reaction II

Automatic evaluation of cyclooxygenase 2 inhibition induced by metal-based anticancer compounds

Synthesis of Hydroxybenzofuranyl-pyrazolyl and Hydroxyphenyl-pyrazolyl Chalcones and Their Corresponding Pyrazoline Derivatives as COX Inhibitors, Anti-inflammatory and Gastroprotective Agents

Dual-target inhibitors based on COX-2: a review from medicinal chemistry perspectives

Novel diphenylthiazole derivatives with multi-target mechanism: Synthesis, docking study, anticancer and anti-inflammatory activities

Fatty Acid Binding to the Allosteric Subunit of Cyclooxygenase-2 Relieves a Tonic Inhibition of the Catalytic Subunit

Synthesis, biological evaluation, molecular docking and theoretical evaluation of ADMET properties of nepodin and chrysophanol derivatives as potential cyclooxygenase (COX-1, COX-2) inhibitors

Human Cyclooxygenase-2 Is a Sequence Homodimer That Functions as a Conformational Heterodimer

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