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Volumn 84, Issue , 2014, Pages 1-7
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Design and synthesis of coumarin-3-acylamino derivatives to scavenge radicals and to protect DNA
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Author keywords
Antioxidant; Coumarin; Coumarin 3 acylamino; DNA; Free radical; Oxidation
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Indexed keywords
2 OXO N PHENETHYL 2H CHROMENE 3 CARBOXAMIDE;
2,2' AZINOBIS(3 ETHYLBENZOTHIAZOLINE 6 SULFONIC ACID);
7 HYDROXY 2 OXO 2H CHROMENE 3 CARBOXYLIC ACID;
7 HYDROXY 2 OXO N PHENETHYL 2H CHROMENE 3 CARBOXAMIDE;
7 HYDROXY 6 METHOXY 2 OXO 2H CHROMENE 3 CARBOXYLIC ACID;
7 HYDROXY 6 METHOXY 2 OXO N PHENETHYL 2H CHROMENE 3 CARBOXAMIDE;
7 HYDROXY N (4 HYDROXYPHENETHYL) 2 OXO 2H CHROMENE 3 CARBOXAMIDE;
ANTIOXIDANT;
COPPER;
COUMARIN 3 ACYLAMINO DERIVATIVE;
COUMARIN 3 CARBOXYL ACID;
COUMARIN DERIVATIVE;
DNA;
GLUTATHIONE;
HYDROXYL GROUP;
N (4 HYDROXYPHENETHYL) 2 OXO 2H 2H CHROMENE 3 CARBOXAMIDE;
UNCLASSIFIED DRUG;
7 HYDROXY N (4 HYDROXYPHENETHYL) 6 METHOXY 2 OXO 2H CHROMENE 3 CARBOXAMIDE;
7 HYDROXY N(4 HYDROXYPHENETHYL) 2 OXO 2H CHROMENE 3 CARBOXAMIDE;
FREE RADICAL;
N (4 HYDROXYPHENETHYL) 2 OXO 2H CHROMENE 3 CARBOXAMIDE;
PHENETHYLAMINE;
TYRAMINE;
SCAVENGER;
ABTS RADICAL SCAVENGING ASSAY;
ANTIOXIDANT ACTIVITY;
ARTICLE;
DRUG DESIGN;
DRUG SYNTHESIS;
OXIDATION;
CARBON NUCLEAR MAGNETIC RESONANCE;
COLUMN CHROMATOGRAPHY;
CONTROLLED STUDY;
DRUG CONJUGATION;
DRUG EFFECT;
HIGH PERFORMANCE LIQUID CHROMATOGRAPHY;
PROTON NUCLEAR MAGNETIC RESONANCE;
THIN LAYER CHROMATOGRAPHY;
CHEMICAL STRUCTURE;
CHEMISTRY;
DOSE RESPONSE;
DRUG EFFECTS;
STRUCTURE ACTIVITY RELATION;
SYNTHESIS;
COUMARINS;
DNA;
DOSE-RESPONSE RELATIONSHIP, DRUG;
DRUG DESIGN;
FREE RADICAL SCAVENGERS;
MOLECULAR STRUCTURE;
STRUCTURE-ACTIVITY RELATIONSHIP;
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EID: 84903996862
PISSN: 02235234
EISSN: 17683254
Source Type: Journal
DOI: 10.1016/j.ejmech.2014.07.009 Document Type: Article |
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Times cited : (27)
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References (39)
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