Quantitative structure-activity relationships predicting the antioxidant potency of 17β-estradiol-related polycyclic phenols to inhibit lipid peroxidation

International Journal of Molecular Sciences

Volumn 14, Issue 1, 2013, Pages 1443-1454

  Prokai, Laszlo ^a   Rivera Portalatin, Nilka M ^a,b   Prokai Tatrai, Katalin ^a  

^a UNIVERSITY OF NORTH TEXAS HEALTH SCIENCE CENTER   (United States)

^b UNIVERSITY OF PUERTO RICO   (Puerto Rico)

Author keywords

17 estradiol; Estrogens; Lipid peroxidation; Oxidative stress; Phenolic antioxidant; QSAR; TBARS

Indexed keywords

ANTIOXIDANT; ESTRADIOL; ESTRONE; FERRIC ION; MALONALDEHYDE; OCTANOL; POLYPHENOL DERIVATIVE; THIOBARBITURIC ACID REACTIVE SUBSTANCE; WATER; ESTROGEN; PHENOL DERIVATIVE; POLYCYCLIC HYDROCARBON;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ANTIOXIDANT ACTIVITY; ARTICLE; BRAIN HOMOGENATE; COMPLEX FORMATION; CONCENTRATION RESPONSE; CONTROLLED STUDY; DISSOCIATION; DRUG DETERMINATION; DRUG IDENTIFICATION; DRUG POTENCY; DRUG STRUCTURE; ELECTRON TRANSPORT; ENERGY; ENTHALPY; HORMONE STRUCTURE; HYDROGEN BOND; IC 50; IN VITRO STUDY; LIPID PEROXIDATION; LIPOPHILICITY; MATHEMATICAL COMPUTING; NERVE DEGENERATION; NONHUMAN; OXIDATIVE STRESS; PARTITION COEFFICIENT; PHYSICAL CHEMISTRY; PROTEIN ANALYSIS; QUANTITATIVE STRUCTURE ACTIVITY RELATION; RAT; ALGORITHM; ANIMAL; BRAIN; CHEMICAL MODEL; CHEMICAL STRUCTURE; CHEMISTRY; DRUG EFFECTS; FEMALE; METABOLISM; OVARIECTOMY; SPRAGUE DAWLEY RAT;

RATTUS;

ALGORITHMS; ANIMALS; ANTIOXIDANTS; BRAIN; ESTRADIOL; ESTROGENS; FEMALE; LIPID PEROXIDATION; MODELS, CHEMICAL; MOLECULAR STRUCTURE; OVARIECTOMY; PHENOLS; POLYCYCLIC COMPOUNDS; QUANTITATIVE STRUCTURE-ACTIVITY RELATIONSHIP; RATS, SPRAGUE-DAWLEY; THIOBARBITURIC ACID REACTIVE SUBSTANCES;

EID: 84878642468     PISSN: 16616596     EISSN: 14220067     Source Type: Journal    
DOI: 10.3390/ijms14011443     Document Type: Article

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