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Volumn 13, Issue 10, 2005, Pages 3439-3445
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Design, synthesis and cytotoxic effect of hydroxy- and 3-alkylaminopropoxy- 9,10-anthraquinone derivatives
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Author keywords
Anthraquinone derivatives; Cytotoxic; Synthesis
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Indexed keywords
1 HYDROXY 3 [3 (ISOPROPYLAMINO)PROPOXYL] 9,10 ANTHRAQUINONE;
1,3 DIHYDROXY 4 PRENYL 9,10 ANTHRAQUINONE;
3 [3 (4 METHYLPIPERAZINOPROPOXY)] 9,10 ANTHRAQUINONE;
3 [3 (BUTYLAMINO)PROPOXY] 1 HYDROXY 9,10 ANTHRAQUINONE;
3 [3 (BUTYLAMINO)PROPOXY] 9,10 ANTHRAQUINONE;
3 [3 (DIETHYLAMINO)PROPOXY] 9,10 ANTHRAQUINONE;
3 [3 (ISOBUTYLAMINO)PROPOXY] 9,10 ANTHRAQUINONE;
3 [3 (ISOPROPYLAMINO)PROPOXY] 9,10 ANTHRAQUINONE;
3 [3 (PROPYLAMINO)PROPOXY] 9,10 ANTHRAQUINONE;
3 [3 (TERT BUTYLAMINO)PROPOXY] 1 HYDROXY 9,10 ANTHRAQUINONE;
3 [3 (TERT BUTYLAMINO)PROPOXY] 9,10 ANTHRAQUINONE;
3 [3 (TERT CYCLOHEXYLAMINO)PROPOXY] 9,10 ANTHRAQUINONE;
ANTHRAQUINONE DERIVATIVE;
DNA FRAGMENT;
UNCLASSIFIED DRUG;
APOPTOSIS;
ARTICLE;
CELL CYCLE G1 PHASE;
CELL DEATH;
CELL STRAIN;
CELL STRAIN HEPG2;
CELL STRAIN MCF 7;
CONCENTRATION RESPONSE;
CONTROLLED STUDY;
CYTOPATHOGENIC EFFECT;
DRUG CYTOTOXICITY;
DRUG DESIGN;
DRUG INHIBITION;
DRUG POTENCY;
DRUG SELECTIVITY;
DRUG STRUCTURE;
DRUG SYNTHESIS;
HUMAN;
HUMAN CELL;
INCUBATION TIME;
STRUCTURE ACTIVITY RELATION;
MINK CELL FOCUS-FORMING VIRUS;
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EID: 17444387763
PISSN: 09680896
EISSN: None
Source Type: Journal
DOI: 10.1016/j.bmc.2005.03.001 Document Type: Article |
Times cited : (30)
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References (12)
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