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1. Full Text In situ click chemistry generation of cyclooxygenase-2 inhibitors
by Bhardwaj, Atul and Kaur, Jatinder and Wuest, Melinda and Wuest, Frank
Nature communications, ISSN 2041-1723, 12/2017, Volume 8, Issue 1, pp. 1 - 14
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Hindlimb | Pyrazoles - chemical synthesis | Humans | Structure-Activity Relationship | Anti-Inflammatory Agents, Non-Steroidal - pharmacology | Thermodynamics | Cyclooxygenase 2 - genetics | Drug Design | Cyclooxygenase 1 - chemistry | Female | Triazoles - chemical synthesis | Anti-Inflammatory Agents, Non-Steroidal - chemical synthesis | Pyrazoles - pharmacology | Cyclooxygenase 2 Inhibitors - chemical synthesis | Cyclooxygenase 1 - genetics | Gene Expression | Cyclooxygenase 2 Inhibitors - pharmacology | Protein Structure, Secondary | Cyclooxygenase 2 - chemistry | Click Chemistry - methods | Rats | Edema - enzymology | Edema - drug therapy | Triazoles - pharmacology | Animals | Cyclooxygenase 2 - metabolism | Molecular Docking Simulation | Carrageenan | Cyclooxygenase 1 - metabolism | Edema - chemically induced | Kinetics | Edema - pathology | Drugs | COX-2 inhibitors | Side effects | Inhibitors | Pain | Cyclooxygenase-1 | Inflammation | Cyclooxygenase-2 | Chemical synthesis | Anti-inflammatory agents | Index Medicus
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2. Full Text Coumarins scaffolds as COX inhibitors
by Revankar, Hrishikesh Mohan and Bukhari, Syed Nasir Abbas and Kumar, Gajjela Bharath and Qin, Hua-Li
Bioorganic chemistry, ISSN 0045-2068, 04/2017, Volume 71, pp. 146 - 159
Coumarins | COX-2 enzymes | Anti-inflammatory | NSAID | COX-1 enzymes | Biochemistry & Molecular Biology | Physical Sciences | Chemistry | Chemistry, Organic | Life Sciences & Biomedicine | Science & Technology | Cyclooxygenase 2 Inhibitors - chemical synthesis | Cyclooxygenase 2 Inhibitors - pharmacology | Antineoplastic Agents - chemical synthesis | Humans | Anti-Inflammatory Agents, Non-Steroidal - chemistry | Coumarins - chemistry | Drug Discovery - methods | Cyclooxygenase Inhibitors - chemistry | Antineoplastic Agents - chemistry | Cyclooxygenase 2 Inhibitors - chemistry | Anti-Inflammatory Agents, Non-Steroidal - pharmacology | Cyclooxygenase Inhibitors - pharmacology | Neoplasms - drug therapy | Coumarins - pharmacology | Animals | Coumarins - chemical synthesis | Cyclooxygenase 2 - metabolism | Cyclooxygenase Inhibitors - chemical synthesis | Antineoplastic Agents - pharmacology | Anti-Inflammatory Agents, Non-Steroidal - chemical synthesis | COX-2 inhibitors | Fluocinolone acetonide | Pharmacy | Medicine, Botanic | Schizophrenia | Drugstores | Medicine, Herbal | Plant metabolites | Index Medicus
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3. Full Text Synthesis and biological evaluation of 3-[4-(amino/methylsulfonyl)phenyl]methylene-indolin-2-one derivatives as novel COX-1/2 and 5-LOX inhibitors
by Lai, Yisheng and Ma, Lin and Huang, Wenxing and Yu, Xing and Zhang, Yihua and Ji, Hui and Tian, Jide
Bioorganic & medicinal chemistry letters, ISSN 0960-894X, 2010, Volume 20, Issue 24, pp. 7349 - 7353
Cyclooxygenase | Amino/methylsufonylphenyl | Anti-inflammatory agents | Indolin-2-one derivatives | 5-Lipoxygenase | Physical Sciences | Chemistry | Chemistry, Organic | Life Sciences & Biomedicine | Pharmacology & Pharmacy | Chemistry, Medicinal | Science & Technology | Biological and medical sciences | Medical sciences | Neuropharmacology | Analgesics | Pharmacology. Drug treatments | Bones, joints and connective tissue. Antiinflammatory agents | Analgesics - pharmacology | Indoles - chemical synthesis | Male | Structure-Activity Relationship | Cyclooxygenase 2 Inhibitors - chemistry | Benzylidene Compounds - chemistry | Lipoxygenase Inhibitors - chemical synthesis | Lipoxygenase Inhibitors - chemistry | Analgesics - chemical synthesis | Arachidonate 5-Lipoxygenase - chemistry | Cyclooxygenase 1 - chemistry | Indoles - pharmacology | Cyclooxygenase 2 Inhibitors - chemical synthesis | Arachidonate 5-Lipoxygenase - metabolism | Cyclooxygenase 2 Inhibitors - pharmacology | Anti-Inflammatory Agents - pharmacology | Cyclooxygenase 2 - chemistry | Rats | Benzylidene Compounds - chemical synthesis | Cyclooxygenase Inhibitors - chemistry | Cyclooxygenase Inhibitors - pharmacology | Animals | Anti-Inflammatory Agents - chemistry | Benzylidene Compounds - pharmacology | Analgesics - chemistry | Cyclooxygenase 2 - metabolism | Cyclooxygenase Inhibitors - chemical synthesis | Anti-Inflammatory Agents - chemical synthesis | Mice | Cyclooxygenase 1 - metabolism | Indoles - chemistry | Lipoxygenase Inhibitors - pharmacology | Index Medicus
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4. Full Text Synthesis, Pharmacological Characterization, and Docking Analysis of a Novel Family of Diarylisoxazoles as Highly Selective Cyclooxygenase‑1 (COX-1) Inhibitors
by Vitale, Paola and Tacconelli, Stefania and Perrone, Maria Grazia and Malerba, Paola and Simone, Laura and Scilimati, Antonio and Lavecchia, Antonio and Dovizio, Melania and Marcantoni, Emanuela and Bruno, Annalisa and Patrignani, Paola
Journal of medicinal chemistry, ISSN 0022-2623, 06/2013, Volume 56, Issue 11, pp. 4277 - 4299
Fibrinolytic Agents - chemistry | Epoprostenol - metabolism | Furans - pharmacology | Humans | Structure-Activity Relationship | Cyclooxygenase 2 Inhibitors - chemistry | Isoxazoles - chemical synthesis | Platelet Aggregation Inhibitors - chemical synthesis | Furans - chemistry | Platelet Aggregation Inhibitors - pharmacology | Thromboxane A2 - antagonists & inhibitors | Female | Fibrinolytic Agents - chemical synthesis | Platelet Aggregation - drug effects | Blood Platelets - drug effects | Thromboxane A2 - biosynthesis | Cyclooxygenase 2 Inhibitors - chemical synthesis | Cell Line | Cyclooxygenase 2 Inhibitors - pharmacology | Mice, Inbred C57BL | Cyclooxygenase Inhibitors - chemistry | Isoxazoles - chemistry | Cyclooxygenase Inhibitors - pharmacology | Isoxazoles - pharmacology | Fibrinolytic Agents - pharmacology | Animals | Blood Platelets - metabolism | Cyclooxygenase 2 - metabolism | Cyclooxygenase Inhibitors - chemical synthesis | Platelet Aggregation Inhibitors - chemistry | Platelet-Rich Plasma | Mice | Molecular Docking Simulation | Cyclooxygenase 1 - metabolism | Furans - chemical synthesis | Index Medicus
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5. Full Text Synthesis of new thiazolo-celecoxib analogues as dual cyclooxygenase-2/15-lipoxygenase inhibitors: Determination of regio-specific different pyrazole cyclization by 2D NMR
by Abdelall, Eman K.A and Kamel, Gehan M
European journal of medicinal chemistry, ISSN 0223-5234, 08/2016, Volume 118, pp. 250 - 258
15-Lipoxygenase inhibitors | Ethyl trifloroacetate | SO2NH2 pharmacophores | Cyclooxygenase inhibitors | Celecoxib analogues | DMFDMA | Anti-inflammatory | pharmacophores | NH | SO | Stereoisomerism | Anti-Inflammatory Agents, Non-Steroidal - chemistry | Male | Cyclooxygenase 2 Inhibitors - chemistry | Celecoxib - chemistry | Anti-Inflammatory Agents, Non-Steroidal - pharmacology | Cyclooxygenase 2 Inhibitors - adverse effects | Lipoxygenase Inhibitors - chemical synthesis | Pyrazoles - chemistry | Lipoxygenase Inhibitors - chemistry | Cattle | Celecoxib - chemical synthesis | Anti-Inflammatory Agents, Non-Steroidal - chemical synthesis | Celecoxib - adverse effects | Cyclooxygenase 2 Inhibitors - chemical synthesis | Chemistry Techniques, Synthetic | Cyclooxygenase 2 Inhibitors - pharmacology | Magnetic Resonance Spectroscopy | Rats | Celecoxib - pharmacology | Arachidonate 15-Lipoxygenase - metabolism | Lipoxygenase Inhibitors - adverse effects | Ulcer - chemically induced | Animals | Anti-Inflammatory Agents, Non-Steroidal - adverse effects | Cyclization | Cyclooxygenase 2 - metabolism | Thiazoles - chemistry | Lipoxygenase Inhibitors - pharmacology | COX-2 inhibitors | Carrageenin | Nuclear magnetic resonance | Celecoxib | Angiogenesis inhibitors | Liability (Law) | Index Medicus
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6. Full Text Novel N-substituted indole Schiff bases as dual inhibitors of cyclooxygenase-2 and 5-lipoxygenase enzymes: Synthesis, biological activities in vitro and docking study
by Lamie, Phoebe F and Ali, Waleed A.M and Bazgier, Vaclav and Rárová, Lucie
European journal of medicinal chemistry, ISSN 0223-5234, 11/2016, Volume 123, pp. 803 - 813
Molecular docking study | Anti-inflammatory activity | Antiproliferative activity | Indole derivatives | Cyclooxygenase enzymes | Antineoplastic Agents - chemical synthesis | Humans | Indoles - chemical synthesis | Cyclooxygenase 2 Inhibitors - chemistry | Anti-Inflammatory Agents - metabolism | Antineoplastic Agents - metabolism | Indoles - metabolism | Lipoxygenase Inhibitors - chemical synthesis | Lipoxygenase Inhibitors - chemistry | Arachidonate 5-Lipoxygenase - chemistry | Drug Design | Indoles - pharmacology | Antineoplastic Agents - pharmacology | Cyclooxygenase 2 Inhibitors - metabolism | Cyclooxygenase 2 Inhibitors - chemical synthesis | Catalytic Domain | Chemistry Techniques, Synthetic | Arachidonate 5-Lipoxygenase - metabolism | Cyclooxygenase 2 Inhibitors - pharmacology | Anti-Inflammatory Agents - pharmacology | Antineoplastic Agents - chemistry | Anti-Inflammatory Agents - chemistry | Schiff Bases - chemistry | Cyclooxygenase 2 - metabolism | Cell Line, Tumor | Anti-Inflammatory Agents - chemical synthesis | Lipoxygenase Inhibitors - metabolism | Molecular Docking Simulation | Cyclooxygenase 1 - metabolism | Indoles - chemistry | Lipoxygenase Inhibitors - pharmacology | Schiff bases | COX-2 inhibitors | Analysis | Phytochemistry | Pharmacy | Drugstores | Nuclear magnetic resonance spectroscopy | Mass spectrometry | Cells | Index Medicus
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7. Full Text Design, synthesis, and biological evaluation of substituted hydrazone and pyrazole derivatives as selective COX-2 inhibitors: Molecular docking study
by El-Sayed, Magda A.-A and Abdel-Aziz, Naglaa I and Abdel-Aziz, Alaa A.-M and El-Azab, Adel S and Asiri, Yousif A and ElTahir, Kamal E.H
Bioorganic & medicinal chemistry, ISSN 0968-0896, 2011, Volume 19, Issue 11, pp. 3416 - 3424
Hydrazone and pyrazole derivatives | Selective COX-2 inhibitors | Molecular docking | Biochemistry & Molecular Biology | Physical Sciences | Chemistry | Chemistry, Organic | Life Sciences & Biomedicine | Pharmacology & Pharmacy | Chemistry, Medicinal | Science & Technology | Biological and medical sciences | Medical sciences | Pharmacology. Drug treatments | Bones, joints and connective tissue. Antiinflammatory agents | Cyclooxygenase 2 Inhibitors - chemical synthesis | Cyclooxygenase 2 Inhibitors - pharmacology | Anti-Inflammatory Agents - pharmacology | Pyrazoles - chemical synthesis | Cyclooxygenase 2 - chemistry | Rats | Edema - drug therapy | Hydrazones - chemical synthesis | Cyclooxygenase 2 Inhibitors - chemistry | Hydrazones - chemistry | Hydrazones - pharmacology | Pyrazoles - chemistry | Animals | Anti-Inflammatory Agents - chemistry | Computer Simulation | Cyclooxygenase 2 - metabolism | Drug Design | Cyclooxygenase 1 - chemistry | Anti-Inflammatory Agents - chemical synthesis | Cyclooxygenase 1 - metabolism | Binding Sites | Disease Models, Animal | Pyrazoles - pharmacology | Index Medicus
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8. Full Text Fragment-based design, docking, synthesis, biological evaluation and structure–activity relationships of 2-benzo/benzisothiazolimino-5-aryliden-4-thiazolidinones as cycloxygenase/lipoxygenase inhibitors
by Eleftheriou, Phaedra and Geronikaki, Athina and Hadjipavlou-Litina, Dimitra and Vicini, Paola and Filz, Olga and Filimonov, Dmitry and Poroikov, Vladimir and Chaudhaery, Shailendra S and Roy, Kuldeep K and Saxena, Anil K
European journal of medicinal chemistry, ISSN 0223-5234, 2012, Volume 47, Issue 1, pp. 111 - 124
Multi-target drugs | Benzo/benzisothiazolidinones | Inflammation | Lipoxygenase inhibitors | COX-1/2 inhibitors | Fragment-based drug design | Thiazolidines - chemical synthesis | Thiazolidines - metabolism | Male | Structure-Activity Relationship | Anti-Inflammatory Agents - metabolism | Lipoxygenase - metabolism | Lipoxygenase Inhibitors - chemical synthesis | Lipoxygenase Inhibitors - chemistry | Drug Design | Cyclooxygenase 1 - chemistry | Female | Thiazolidines - pharmacology | Thiazolidines - chemistry | Catalytic Domain | Cyclooxygenase Inhibitors - metabolism | Anti-Inflammatory Agents - pharmacology | Cyclooxygenase 2 - chemistry | Models, Molecular | Cyclooxygenase Inhibitors - chemistry | Edema - drug therapy | Lipoxygenase - chemistry | Cyclooxygenase Inhibitors - pharmacology | Animals | Anti-Inflammatory Agents - chemistry | Cyclooxygenase 2 - metabolism | Cyclooxygenase Inhibitors - chemical synthesis | Anti-Inflammatory Agents - chemical synthesis | Lipoxygenase Inhibitors - metabolism | Mice | Cyclooxygenase 1 - metabolism | Edema - chemically induced | Lipoxygenase Inhibitors - pharmacology | COX-2 inhibitors | Enzymes | Index Medicus
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9. Full Text Cyclooxygenase-1-Selective Inhibitors Based on the (E)-2′-Des-methyl-sulindac Sulfide Scaffold
by Liedtke, Andy J and Crews, Brenda C and Daniel, Cristina M and Blobaum, Anna L and Kingsley, Philip J and Ghebreselasie, Kebreab and Marnett, Lawrence J
Journal of medicinal chemistry, ISSN 0022-2623, 03/2012, Volume 55, Issue 5, pp. 2287 - 2300
Stereoisomerism | Antineoplastic Agents - chemical synthesis | Humans | Structure-Activity Relationship | Cyclooxygenase 2 Inhibitors - chemistry | Female | Antineoplastic Agents - pharmacology | Cyclooxygenase 2 Inhibitors - chemical synthesis | Cyclooxygenase 2 Inhibitors - pharmacology | Sulindac - chemistry | Cyclooxygenase Inhibitors - chemistry | Antineoplastic Agents - chemistry | Cyclooxygenase Inhibitors - pharmacology | Sulindac - analogs & derivatives | Animals | Cyclooxygenase Inhibitors - chemical synthesis | Cell Line, Tumor | Hydrophobic and Hydrophilic Interactions | Sheep | Cell Proliferation - drug effects | Mice | Cyclooxygenase 1 - metabolism | Sulindac - chemical synthesis | Sulindac - pharmacology | Drug Screening Assays, Antitumor | Index Medicus
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10. Full Text 1,2,3-Triazolyl ester of Ketorolac: A “Click Chemistry”-based highly potent PAK1-blocking cancer-killer
by Nguyen, Binh Cao Quan and Takahashi, Hideaki and Uto, Yoshihiro and Shahinozzaman, M.d and Tawata, Shinkichi and Maruta, Hiroshi
European journal of medicinal chemistry, ISSN 0223-5234, 01/2017, Volume 126, pp. 270 - 276
Triazole ring | PAK1 | Click chemistry | COX-2 | Ketorolac | Cancer | Triazoles - chemistry | Antineoplastic Agents - chemical synthesis | Humans | p21-Activated Kinases - antagonists & inhibitors | Cyclooxygenase 2 Inhibitors - chemistry | Ketorolac - chemistry | Antineoplastic Agents - metabolism | Ketorolac - metabolism | Protein Kinase Inhibitors - chemistry | Biological Transport | Esters - chemistry | Antineoplastic Agents - pharmacology | Cyclooxygenase 2 Inhibitors - metabolism | Cyclooxygenase 2 Inhibitors - chemical synthesis | Protein Kinase Inhibitors - chemical synthesis | Cyclooxygenase 2 Inhibitors - pharmacology | Click Chemistry | Antineoplastic Agents - chemistry | p21-Activated Kinases - metabolism | Ketorolac - chemical synthesis | Signal Transduction - drug effects | Cell Line, Tumor | Protein Kinase Inhibitors - pharmacology | Ketorolac - pharmacology | Protein Kinase Inhibitors - metabolism | COX-2 inhibitors | Prostaglandins | Melanoma | Permeability | Nonsteroidal anti-inflammatory drugs | Drug resistance | Triazoles | Index Medicus
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11. Full Text Antimicrobial and selected in vitro enzyme inhibitory effects of leaf extracts, flavonols and indole alkaloids isolated from Croton menyharthii
by Aderogba, Mutalib A and Ndhlala, Ashwell R and Rengasamy, Kannan R.R and Van Staden, Johannes
Molecules (Basel, Switzerland), ISSN 1420-3049, 10/2013, Volume 18, Issue 10, pp. 12633 - 12644
Antimicrobial | Flavonols | Alkaloid | COX-2 | Croton menyharthii Pax | Alpha-glucosidase | Mutagenicity | Biochemistry & Molecular Biology | Physical Sciences | Chemistry | Life Sciences & Biomedicine | Chemistry, Multidisciplinary | Science & Technology | Plant Extracts - chemistry | Plant Extracts - pharmacology | Escherichia coli - drug effects | Humans | Alkaloids - isolation & purification | Cholinesterase Inhibitors - chemistry | Antifungal Agents - chemistry | Flavonols - isolation & purification | Indoles - isolation & purification | Cyclooxygenase 2 Inhibitors - chemistry | Microbial Sensitivity Tests | Candida albicans - drug effects | Anti-Bacterial Agents - chemistry | Inhibitory Concentration 50 | Indoles - pharmacology | Cholinesterase Inhibitors - isolation & purification | Antifungal Agents - pharmacology | Plant Leaves - chemistry | Alkaloids - pharmacology | Cyclooxygenase 2 Inhibitors - pharmacology | Fish Proteins - chemistry | Cyclooxygenase 2 - chemistry | Cyclooxygenase 2 Inhibitors - isolation & purification | Electrophorus | Plant Extracts - isolation & purification | Acetylcholinesterase - chemistry | Anti-Bacterial Agents - isolation & purification | Flavonols - chemistry | Antifungal Agents - isolation & purification | Animals | Cholinesterase Inhibitors - pharmacology | Croton - chemistry | Anti-Bacterial Agents - pharmacology | Flavonols - pharmacology | Staphylococcus aureus - drug effects | Indoles - chemistry | Alkaloids - chemistry | Bacillus subtilis - drug effects | Index Medicus | antimicrobial | mutagenicity | alpha-glucosidase | flavonols | alkaloid
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12. Full Text 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
by Xie, Linlin and Lee, David Yue-wei and Shang, Ying and Cao, Xiaotong and Wang, Siqi and Liao, Jun and Zhang, Teng and Dai, Ronghua
Phytomedicine (Stuttgart), ISSN 0944-7113, 10/2020, Volume 77, pp. 153284 - 153284
Saponins | AUF-LC-MS | Inflammation | Cyclooxygenase-2 | 5-lipoxygenase | Dual targeted inhibitors | Pharmacology & Pharmacy | Life Sciences & Biomedicine | Chemistry, Medicinal | Integrative & Complementary Medicine | Plant Sciences | Science & Technology | Spirostans - pharmacology | Arachidonate 5-Lipoxygenase - genetics | Anti-Inflammatory Agents, Non-Steroidal - chemistry | Chromatography, High Pressure Liquid | Cyclooxygenase 2 Inhibitors - chemistry | Saponins - chemistry | Anti-Inflammatory Agents, Non-Steroidal - pharmacology | Ultrafiltration | Anemarrhena - chemistry | Lipoxygenase Inhibitors - chemistry | Rhizome - chemistry | Cyclooxygenase 2 - genetics | Inflammation - drug therapy | Mass Spectrometry | Arachidonate 5-Lipoxygenase - chemistry | Steroids - pharmacology | Spirostans - chemistry | Drug Evaluation, Preclinical | Glycosides - chemistry | Steroids - chemistry | Sterols - pharmacology | Arachidonate 5-Lipoxygenase - metabolism | Cyclooxygenase 2 Inhibitors - pharmacology | Sterols - chemistry | Cyclooxygenase 2 - chemistry | Rats | Glycosides - pharmacology | Animals | Cyclooxygenase 2 - metabolism | Molecular Docking Simulation | Lipoxygenase Inhibitors - pharmacology | Saponins - pharmacology | Index Medicus
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