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Volumn 21, Issue 15, 2013, Pages 4581-4590
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Synthesis of novel celecoxib analogues by bioisosteric replacement of sulfonamide as potent anti-inflammatory agents and cyclooxygenase inhibitors
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Author keywords
1,5 Diarylpyrazoles; Anti inflammatory activity; Bioisostere; Carbothioamide; Cyclooxygenase inhibitors; Inflammation; NSAIDs; Sulfonamide
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Indexed keywords
4 [5 (4 BROMOPHENYL) 3 (TRIFLUOROMETHYL) 1H PYRAZOL 1 YL]BENZENECARBOTHIOAMIDE;
4 [5 (4 BROMOPHENYL) 3 (TRIFLUOROMETHYL) 1H PYRAZOL 1 YL]BENZONITRILE;
4 [5 (4 CHLOROPHENYL) 3 (TRIFLUOROMETHYL) 1H PYRAZOL 1 YL]BENZENECARBOTHIOAMIDE;
4 [5 (4 CHLOROPHENYL) 3 (TRIFLUOROMETHYL) 1H PYRAZOL 1 YL]BENZONITRILE;
4 [5 (4 FLUOROPHENYL) 3 (TRIFLUOROMETHYL) 1H PYRAZOL 1 YL]BENZENECARBOTHIOAMIDE;
4 [5 (4 FLUOROPHENYL) 3 (TRIFLUOROMETHYL) 1H PYRAZOL 1 YL]BENZONITRILE;
4 [5 (4 METHOXYPHENYL) 3 (TRIFLUOROMETHYL) 1H PYRAZOL 1 YL]BENZENECARBOTHIOAMIDE;
4 [5 (4 METHOXYPHENYL) 3 (TRIFLUOROMETHYL) 1H PYRAZOL 1 YL]BENZONITRILE;
4 [5 (4 METHYLPHENYL) 3 (TRIFLUOROMETHYL) 1H PYRAZOL 1 YL]BENZENECARBOTHIOAMIDE;
4 [5 (4 METHYLPHENYL) 3 (TRIFLUOROMETHYL) 1H PYRAZOL 1 YL]BENZONITRILE;
4 [5 (FURAN 2 YL) 3 (TRIFLUOROMETHYL) 1H PYRAZOL 1 YL]BENZENECARBOTHIOAMIDE;
4 [5 (FURAN 2 YL) 3 (TRIFLUOROMETHYL) 1H PYRAZOL 1 YL]BENZONITRILE;
4 [5 (NAPHTHALEN 2 YL) 3 (TRIFLUOROMETHYL) 1H PYRAZOL 1 YL]BENZENECARBOTHIOAMIDE;
4 [5 (NAPHTHALEN 2 YL) 3 (TRIFLUOROMETHYL) 1H PYRAZOL 1 YL]BENZONITRILE;
4 [5 (THIOPHEN 2 YL) 3 (TRIFLUOROMETHYL) 1H PYRAZOL 1 YL]BENZENECARBOTHIOAMIDE;
4 [5 (THIOPHEN 2 YL) 3 (TRIFLUOROMETHYL) 1H PYRAZOL 1 YL]BENZONITRILE;
4 [5 PHENYL 3 (TRIFLUOROMETHYL) 1H PYRAZOL 1 YL]BENZENECARBOTHIOAMIDE;
4 [5 PHENYL 3 (TRIFLUOROMETHYL) 1H PYRAZOL 1 YL]BENZONITRILE;
ANTIINFLAMMATORY AGENT;
CARRAGEENAN;
CELECOXIB;
CELECOXIB DERIVATIVE;
CYCLOOXYGENASE 1;
CYCLOOXYGENASE 2;
INDOMETACIN;
PROSTAGLANDIN SYNTHASE INHIBITOR;
UNCLASSIFIED DRUG;
ANIMAL CELL;
ANIMAL EXPERIMENT;
ANIMAL MODEL;
ANIMAL TISSUE;
ANTIINFLAMMATORY ACTIVITY;
ARTICLE;
BIOISOSTERE;
CHEMICAL STRUCTURE;
CONCENTRATION RESPONSE;
CONTROLLED STUDY;
DRUG POTENCY;
DRUG PROTEIN BINDING;
DRUG SCREENING;
DRUG STRUCTURE;
DRUG SYNTHESIS;
ENZYME ASSAY;
ENZYME INHIBITION;
IC 50;
IN VITRO STUDY;
IN VIVO STUDY;
MALE;
MOLECULAR DOCKING;
NONHUMAN;
PAW EDEMA;
RAT;
TREATMENT OUTCOME;
RATTUS;
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EID: 84879688131
PISSN: 09680896
EISSN: 14643391
Source Type: Journal
DOI: 10.1016/j.bmc.2013.05.029 Document Type: Article |
Times cited : (69)
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References (37)
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