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Volumn 25, Issue 2, 2017, Pages 665-676
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Design, synthesis and analgesic/anti-inflammatory evaluation of novel diarylthiazole and diarylimidazole derivatives towards selective COX-1 inhibitors with better gastric profile
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Author keywords
Analgesic; Anti inflammatory; Diarylimidazole; Diarylthiazole; Mofezolac; Selective COX 1; Ulcerogenicity
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Indexed keywords
(4,5 DIPHENYLTHIAZOL 2 YL)GLYCINE;
2 (4,5 DIPHENYL 1H IMIDAZOL 1 YL) 1 (4 METHYLPIPERAZIN 1 YL)ETHANONE;
2 (4,5 DIPHENYL 1H IMIDAZOL 1 YL) 1 (PIPERIDIN 1 YL)ETHANONE;
2 (4,5 DIPHENYL 1H IMIDAZOL 1 YL) 1 MORPHOLINOETHANONE;
2 (4,5 DIPHENYL 1H IMIDAZOL 1 YL)ACETIC ACID;
2 [(4,5 DIPHENYLTHIAZOL 2 YL)AMINO] 1 (4 METHYLPIPERAZIN 1 YL)ETHANONE;
2 [(4,5 DIPHENYLTHIAZOL 2 YL)AMINO] 1 (PIPERIDIN 1 YL)ETHANONE;
2 [(4,5 DIPHENYLTHIAZOL 2 YL)AMINO] 1 MORPHOLINOETHANONE;
2 [4,5 BIS(4 METHOXYPHENYL) 1H IMIDAZOL 1 YL] 1 (4 METHYLPIPERAZIN 1 YL)ETHANONE;
2 [4,5 BIS(4 METHOXYPHENYL) 1H IMIDAZOL 1 YL] 1 (PIPERIDIN 1 YL)ETHANONE;
2 [4,5 BIS(4 METHOXYPHENYL) 1H IMIDAZOL 1 YL] 1 MORPHOLINOETHANONE;
2 [4,5 BIS(4 METHOXYPHENYL) 1H IMIDAZOL 1 YL]ACETIC ACID;
2 [[4,5 BIS(4 METHOXYPHENYL)THIAZOL 2 YL]AMINO] 1 (4 METHYLPIPERAZIN 1 YL)ETHANONE;
2 [[4,5 BIS(4 METHOXYPHENYL)THIAZOL 2 YL]AMINO] 1 (PIPERIDIN 1 YL)ETHANONE;
2 [[4,5 BIS(4 METHOXYPHENYL)THIAZOL 2 YL]AMINO] 1 MORPHOLINOETHANONE;
4,5 BIS(4 METHOXYPHENYL) 1H IMIDAZOLE;
4,5 DIARYLTHIAZOLE DERIVATIVE;
4,5 DIPHENYL 1H IMIDAZOLE;
ANALGESIC AGENT;
ANTIINFLAMMATORY AGENT;
CELECOXIB;
CYCLOOXYGENASE 1 INHIBITOR;
DIARYLIMIDAZOLE DERIVATIVE;
DICLOFENAC;
ETHYL 2 [(4,5 BIS(4 METHOXYPHENYL)THIAZOL 2 YL)AMINO]ACETATE;
FR 122047;
INDOMETACIN;
MOFEZOLAC;
UNCLASSIFIED DRUG;
UNINDEXED DRUG;
[4,5 BIS(4 METHOXYPHENYL)THIAZOL 2 YL]GLYCINE;
ACETIC ACID;
CARRAGEENAN;
CYCLOOXYGENASE 1;
IMIDAZOLE DERIVATIVE;
NONSTEROID ANTIINFLAMMATORY AGENT;
PROSTAGLANDIN SYNTHASE INHIBITOR;
THIAZOLE DERIVATIVE;
ADULT;
ANALGESIC ACTIVITY;
ANIMAL EXPERIMENT;
ANIMAL MODEL;
ANTIINFLAMMATORY ACTIVITY;
ARTICLE;
CARRAGEENAN-INDUCED PAW EDEMA;
CLINICAL EFFECTIVENESS;
CONCENTRATION RESPONSE;
CONTROLLED STUDY;
DRUG DESIGN;
DRUG SAFETY;
DRUG STRUCTURE;
DRUG SYNTHESIS;
DRUG TOLERANCE;
FEMALE;
IN VITRO STUDY;
IN VIVO STUDY;
MALE;
MOLECULAR DOCKING;
NONHUMAN;
RAT;
ULCEROGENESIS;
WRITHING TEST;
ANIMAL;
BOVINE;
CHEMICAL STRUCTURE;
CHEMICALLY INDUCED;
CHEMISTRY;
DOSE RESPONSE;
EDEMA;
ENZYMOLOGY;
HUMAN;
METABOLISM;
PAIN;
STOMACH MUCOSA;
STRUCTURE ACTIVITY RELATION;
SYNTHESIS;
ACETIC ACID;
ANALGESICS;
ANIMALS;
ANTI-INFLAMMATORY AGENTS, NON-STEROIDAL;
CARRAGEENAN;
CATTLE;
CYCLOOXYGENASE 1;
CYCLOOXYGENASE INHIBITORS;
DOSE-RESPONSE RELATIONSHIP, DRUG;
DRUG DESIGN;
EDEMA;
FEMALE;
GASTRIC MUCOSA;
HUMANS;
IMIDAZOLES;
MALE;
MOLECULAR DOCKING SIMULATION;
MOLECULAR STRUCTURE;
PAIN;
RATS;
STRUCTURE-ACTIVITY RELATIONSHIP;
THIAZOLES;
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EID: 85007251540
PISSN: 09680896
EISSN: 14643391
Source Type: Journal
DOI: 10.1016/j.bmc.2016.11.037 Document Type: Article |
Times cited : (43)
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References (32)
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