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Volumn 340, Issue 3, 2007, Pages 147-153
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Synthesis and in vitro cytotoxicity evaluation of novel naphthindolizinedione derivatives
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Author keywords
Antitumor activity; Cytotoxic activity; DNA topoisomerases; Polycyclic amines; Synthesis
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Indexed keywords
12 [4 (2 HYDROXY ETHYL)PIPERAZINE 1 CARBONYL] BENZO[F]PYRIDO[1,2 A]INDOLE 6,11 DIONE;
6,11 DIOXO 6,11 DIHYDRO BENZO[F]PYRIDO[1,2 A]INDOLE(2 DIETHYLAMINO ETHYL) 12 CARBOXAMIDE;
6,11 DIOXO 6,11 DIHYDRO BENZO[F]PYRIDO[1,2 A]INDOLE(2 DIMETHYLAMINO ETHYL) 12 CARBOXAMIDE;
7,10 DIHYDROXY 12 [4 (2 HYDROXY ETHYL)PIPERAZINE 1 CARBONYL]BENZO[F]PYRIDO[1,2 A]INDOLE 6,11 DIONE;
7,10 DIHYDROXY 6,11 DIOXO 6,11 DIHYDRO BENZO[F]PYRIDO[1,2 A]INDOLE(2 DIETHYLAMINO ETHYL) 12 CARBOXAMIDE;
7,10 DIHYDROXY 6,11 DIOXO 6,11 DIHYDRO BENZO[F]PYRIDO[1,2 A]INDOLE(2 DIMETHYLAMINO ETHYL) 12 CARBOXAMIDE;
AMIDE;
AMINOACRIDINE DERIVATIVE;
CARBOXYLIC ACID DERIVATIVE;
DAUNORUBICIN;
DOXORUBICIN;
ELLIPTICINE;
ETHYL 7,10 DIHYDROXY 6,11 DIOXO 6,11 DIHYDRO BENZO[F]PYRIDO[1,2 A]INDOLE 12 CARBOXYLATE;
INDOLIZIDINE DERIVATIVE;
MITOXANTRONE;
UNCLASSIFIED DRUG;
ANTINEOPLASTIC AGENT;
INDOLIZINE DERIVATIVE;
INTERCALATING AGENT;
ANTINEOPLASTIC ACTIVITY;
ARTICLE;
BREAST TUMOR;
CHEMICAL MODIFICATION;
COLON CANCER;
CONTROLLED STUDY;
CYTOTOXICITY;
DRUG MECHANISM;
DRUG POTENCY;
DRUG SCREENING;
DRUG SELECTIVITY;
DRUG STRUCTURE;
DRUG SYNTHESIS;
HUMAN;
HUMAN CELL;
IN VITRO STUDY;
KIDNEY CANCER;
LEUKEMIA;
PRIORITY JOURNAL;
CELL PROLIFERATION;
CHEMICAL STRUCTURE;
DOSE RESPONSE;
DRUG DESIGN;
DRUG EFFECT;
IC 50;
STRUCTURE ACTIVITY RELATION;
SYNTHESIS;
TUMOR CELL LINE;
ANTINEOPLASTIC AGENTS;
CELL LINE, TUMOR;
CELL PROLIFERATION;
DOSE-RESPONSE RELATIONSHIP, DRUG;
DRUG DESIGN;
HUMANS;
INDOLIZINES;
INHIBITORY CONCENTRATION 50;
INTERCALATING AGENTS;
MOLECULAR STRUCTURE;
STRUCTURE-ACTIVITY RELATIONSHIP;
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EID: 34250352377
PISSN: 03656233
EISSN: 15214184
Source Type: Journal
DOI: 10.1002/ardp.200600160 Document Type: Article |
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Times cited : (11)
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References (16)
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