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Volumn 46, Issue 7, 2011, Pages 2797-2806
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Identification of 5-arylidene-4-thiazolidinone derivatives endowed with dual activity as aldose reductase inhibitors and antioxidant agents for the treatment of diabetic complications
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Author keywords
5 arylidene 4 thiazolidinones; Aldose reductase; Antioxidant agent; Diabetes mellitus; Molecular docking
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Indexed keywords
4 THIAZOLIDINONE DERIVATIVE;
5 (3 PHENYL 2 PROPEN 1 YLIDENE) 2,4 THIAZOLIDINEDIONE;
5 [3 (4 METHOXYPHENYL) 2 PROPEN 1 YLIDENE] 2,4 THIAZOLIDINEDIONE;
5 [3 (4 METHYLPHENYL) 2 PROPEN 1 YLIDENE] 2,4 THIAZOLIDINEDIONE;
5 [3 (4 TRIFLUOROMETHYLPHENYL) 2 PROPEN 1 YLIDENE] 2,4 THIAZOLIDINEDIONE;
5 [[ 4 (2 PHENYLETHENYL)PHENYL]METHYLIDENE] 2,4 THIAZOLIDINEDIONE;
5 [[[4 [2 (4 METHOXYPHENYL)]ETHENYL]PHENYL]METHYLIDENE) 2,4 THIAZOLIDINEDIONE;
5 [[[4 [2 (4 METHYLPHENYL)]ETHENYL]PHENYL]METHYLIDENE] 2,4 THIAZOLIDINEDIONE;
5 [[[4 [2 (4 TRIFLUOROMETHYLPHENYL)]ETHENYL]PHENYL]METHYLIDENE] 2,4 THIAZOLIDINEDIONE;
[2,4 DIOXO 5 (3 PHENYL 2 PROPEN 1 YLIDENE)THIAZOLIDIN 3 YL]ACETIC ACID;
[2,4 DIOXO 5 [[4 (2 PHENYLETHENYL)PHENYL]METHYLIDENE]THIAZOLIDIN 3 YL]ACETIC ACID;
[4 OXO 5 (4 PHENOXYPHENYLMETHYLIDENE) 2 PHENYLIMINOTHIAZOLIDIN 3 YL]ACETIC ACID;
[5 (4 BENZYLOXYPHENYLMETHYLIDENE) 4 OXO 2 PHENYLIMINOTHIAZOLIDIN 3 YL]ACETIC ACID;
[5 (NAPHTALEN 2 YLMETHYLIDENE) 4 OXO 2 PHENYLIMINOTHIAZOLIDIN 3 YL]ACETIC ACID;
[5 [3 (4 METHOXYPHENYL) 2 PROPEN 1 YLIDENE] 2,4 DIOXOTHIAZOLIDIN 3 YL]ACETIC ACID;
[5 [3 (4 TRIFLUOROMETHYLPHENYL) 2 PROPEN 1 YLIDENE] 2,4 DIOXOTHIAZOLIDIN 3 YL]ACETIC ACID;
[5 [[4 [2 (4 METHOXYPHENYL)ETHENYL]PHENYL]METHYLIDENE] 2,4 DIOXOTHIAZOLIDIN 3 YL]ACETIC ACID;
[5 [[4 [2 (4 METHYLPHENYL)ETHENYL]PHENYL]METHYLIDENE] 2,4 DIOXOTHIAZOLIDIN 3 YL]ACETIC ACID;
[5 [[4 [2 (4 TRIFLUOROMETHYLPHENYL)ETHENYL]PHENYL]METHYLIDENE] 2,4 DIOXOTHIAZOLIDIN 3 YL]ACETIC ACID;
ALDOSE REDUCTASE INHIBITOR;
UNCLASSIFIED DRUG;
2,4 THIAZOLIDINEDIONE DERIVATIVE;
ACETIC ACID DERIVATIVE;
ALDEHYDE REDUCTASE;
ANTIOXIDANT;
ENZYME INHIBITOR;
ANIMAL TISSUE;
ANTIOXIDANT ACTIVITY;
ARTICLE;
DIABETES MELLITUS;
DRUG ACTIVITY;
DRUG SYNTHESIS;
ENZYME INHIBITION;
IC 50;
IN VITRO STUDY;
MOLECULAR DOCKING;
NONHUMAN;
OXIDATIVE STRESS;
STRUCTURE ACTIVITY RELATION;
ANIMAL;
ANTAGONISTS AND INHIBITORS;
BOVINE;
CHEMISTRY;
DIABETES COMPLICATIONS;
DRUG EFFECTS;
HUMAN;
SYNTHESIS;
ACETATES;
ALDEHYDE REDUCTASE;
ANIMALS;
ANTIOXIDANTS;
CATTLE;
DIABETES COMPLICATIONS;
ENZYME INHIBITORS;
HUMANS;
MOLECULAR DOCKING SIMULATION;
OXIDATIVE STRESS;
STRUCTURE-ACTIVITY RELATIONSHIP;
THIAZOLIDINEDIONES;
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EID: 79957463623
PISSN: 02235234
EISSN: 17683254
Source Type: Journal
DOI: 10.1016/j.ejmech.2011.03.068 Document Type: Article |
Times cited : (112)
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References (35)
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