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Volumn 85, Issue , 2014, Pages 107-118
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Design and synthesis of azaisoflavone analogs as phytoestrogen mimetics
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Author keywords
Azaisoflavones; ER agonist; Estrogen receptor; Proliferation
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Indexed keywords
1 (2 AMINO 4 METHOXYPHENYL) 3 (4 METHOXYPHENYL)PROPENONE;
1 (2 AMINO 4 METHOXYPHENYL)ETHANONE;
1 (2 AMINO 4,6 DIMETHOXYPHENYL) 3 (4 METHOXYPHENYL)PROPENONE;
1 (2 AMINO 4,6 DIMETHOXYPHENYL)ETHANONE;
1 (2 AMINOPHENYL) 3 (4 METHOXYPHENYL)PROPENONE;
1 (2 AMINOPHENYL)ETHANONE;
1 ETHYL 3 (4 HYDROXYPHENYL) 1H QUINOLIN 4 ONE;
1 METHYL 3 (4 HYDROXYPHENYL) 1H QUINOLIN 4 ONE;
1 PROPYL 3 (4 HYDROXYPHENYL) 1H QUINOLIN 4 ONE;
3(4 HYDROXYPHENYL) 1H QUINOLIN 4 ONE;
5,7 DIHYDROXY 3 (4 HYDROXYPHENYL) 1 ETHYL 1H QUINOLIN 4 ONE;
5,7 DIHYDROXY 3 (4 HYDROXYPHENYL) 1 METHYL 1H QUINOLIN 4 ONE;
5,7 DIHYDROXY 3 (4 HYDROXYPHENYL) 1 PROPYL 1H QUINOLIN 4 ONE;
5,7 DIHYDROXY 3 (4 HYDROXYPHENYL) 1H QUINOLIN 4 ONE;
7 HYDROXY 3 (4 HYDROXYPHENYL) 1 (3 METHYLBUTYL) 1H QUINOLIN 4 ONE;
7 HYDROXY 3 (4 HYDROXYPHENYL) 1 BENZYL 1H QUINOLIN 4 ONE;
7 HYDROXY 3 (4 HYDROXYPHENYL) 1 ETHYL 1H QUINOLIN 4 ONE;
7 HYDROXY 3 (4 HYDROXYPHENYL) 1 METHYL 1H QUINOLIN 4 ONE;
7 HYDROXY 3 (4 HYDROXYPHENYL) 1 PROPYL 1H QUINOLIN 4 ONE;
7 HYDROXY 3 (4 HYDROXYPHENYL) 1H QUINOLIN 4 ONE;
AZAISOFLAVONE DERIVATIVE;
GENISTEIN;
ISOFLAVONE DERIVATIVE;
N [2 [3 (4 METHOXYPHENYL) 1 OXO 2 PROPENYL]PHENYL]ACETAMIDE;
N [2 [3,3 DIMETHOXY 2 (4 METHOXYPHENYL) 1 OXOPROPYL]PHENYL]ACETAMIDE;
N {2 [3,3 DIMETHOXY 2 (4 METHOXYPHENYL)PROPIONYL] 5 METHOXYPHENYL}ACETAMIDE;
N {3,5 DIMETHOXY 2 [3 (4 METHOXYPHENYL)ACRYLOYL]PHENYL}ACETAMIDE;
N {5 METHOXY 2 [3 (4 METHOXYPHENYL)ACRYLOYL]PHENYL}ACETAMIDE;
PHYTOESTROGEN;
UNCLASSIFIED DRUG;
UNINDEXED DRUG;
1METHYL 3 (4 HYDROXYPHENYL) 1H QUINOLIN 4 ONE;
3 (4 HYDROXYPHENYL) 1H QUINOLIN 4 ONE;
3 (4 METHOXYPHENYL) 1 ETHYL 1H QUINOLIN 4 ONE;
3 (4 METHOXYPHENYL) 1 METHYL 1H QUINOLIN 4 ONE;
3 (4 METHOXYPHENYL) 1 PROPYL 1H QUINOLIN 4 ONE;
3 (4 METHOXYPHENYL) 4(1H) QUINOLINONE;
5,7 DIMETHOXY 3 (4 METHOXYPHENYL) 1 ETHYL 1H QUINOLIN 4 ONE;
5,7 DIMETHOXY 3 (4 METHOXYPHENYL) 1 METHYL 1H QUINOLIN 4 ONE;
5,7 DIMETHOXY 3 (4 METHOXYPHENYL) 1 PROPYL 1H QUINOLIN 4 ONE;
5,7 DIMETHOXY 3 (4 METHOXYPHENYL) 1H QUINOLIN 4 ONE;
7 METHOXY 3 (4 METHOXY PHENYL) 1 ETHYL 1H QUINOLIN 4 ONE;
7 METHOXY 3 (4 METHOXYPHENYL) 1 METHYL 1H QUINOLIN 4 ONE;
7 METHOXY 3 (4 METHOXYPHENYL) 1 PROPYL 1H QUINOLIN 4 ONE;
7 METHOXY 3 (4 METHOXYPHENYL) 2,3 DIHYDRO 1H QUINOLIN 4 ONE;
ESTROGEN RECEPTOR ALPHA;
ESTROGEN RECEPTOR BETA;
FLAVONE DERIVATIVE;
QUINOLONE DERIVATIVE;
ALKYLATION;
ANTIPROLIFERATIVE ACTIVITY;
ARTICLE;
BREAST CANCER;
CANCER CELL;
CANCER GROWTH;
CARBON NUCLEAR MAGNETIC RESONANCE;
CELL GROWTH;
CELL PROLIFERATION;
CONTROLLED STUDY;
DRUG DESIGN;
DRUG SYNTHESIS;
ESTROGEN ACTIVITY;
HUMAN;
IN VITRO STUDY;
MCF 7 CELL LINE;
MOLECULAR MODEL;
PROTON NUCLEAR MAGNETIC RESONANCE;
TRANSACTIVATION ASSAY;
BINDING AFFINITY;
TRANSACTIVATION;
CHEMISTRY;
DOSE RESPONSE;
DRUG EFFECTS;
ENZYME ACTIVE SITE;
GENETICS;
METABOLISM;
MOLECULAR DOCKING;
STRUCTURE ACTIVITY RELATION;
SYNTHESIS;
TRANSCRIPTION INITIATION;
CATALYTIC DOMAIN;
CELL PROLIFERATION;
CHEMISTRY TECHNIQUES, SYNTHETIC;
DOSE-RESPONSE RELATIONSHIP, DRUG;
DRUG DESIGN;
ESTROGEN RECEPTOR ALPHA;
ESTROGEN RECEPTOR BETA;
FLAVONES;
HUMANS;
MCF-7 CELLS;
MOLECULAR DOCKING SIMULATION;
PHYTOESTROGENS;
QUINOLONES;
STRUCTURE-ACTIVITY RELATIONSHIP;
TRANSCRIPTIONAL ACTIVATION;
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EID: 84905182093
PISSN: 02235234
EISSN: 17683254
Source Type: Journal
DOI: 10.1016/j.ejmech.2014.07.030 Document Type: Article |
Times cited : (15)
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References (40)
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