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Volumn 13, Issue 6, 2002, Pages 567-581
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Among substituted 9,10-dihydro-9,10-[1,2]benzenoanthracene-1,4,5,8-tetraones, the lead antitumor triptycene bisquinone TT24 blocks nucleoside transport, induces apoptotic DNA fragmentation and decreases the viability of L1210 leukemic cells in the nanomolar range of daunorubicin in vitro
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Author keywords
Apoptosis; DNA synthesis and fragmentation; L1210 cells; Nucleoside transport; Triptycene bisquinones; Tumor cell viability
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Indexed keywords
2 BROMO 3 METHOXY 9,10 DIHYDRO 9,10 [1',2']BENZENOANTHRACENE 1,4,5,8 TETRAONE;
2 METHOXY 9,10 DIHYDRO 9,10 [1',2']BENZENOANTHRACENE 1,4,5,8 TETRAONE;
6 BROMO 7 METHOXY 2 N DIMETHYLAMINO 9,10 DIHYDRO 9,10 [1',2']BENZENOANTHRACENE 1,4,5,8 TETRAONE;
6 BROMO 7 METHOXY 2 N METHYLAMINO 9,10 DIHYDRO 9,10 [1',2']BENZENOANTHRACENE 1,4,5,8 TETRAONE;
7 BROMO 6 METHOXY 2 N DIMETHYLAMINO 9,10 DIHYDRO 9,10 [1',2']BENZENOANTHRACENE 1,4,5,8 TETRAONE;
7 BROMO 6 METHOXY 2 N METHYLAMINO 9,10 DIHYDRO 9,10 [1',2']BENZENOANTHRACENE 1,4,5,8 TETRAONE;
9,10 DIHYDRO 9,10 [1,2]BENZENOANTHRACENE 1,4,5,8 TETRAONE;
ANTHRACYCLINE ANTIBIOTIC AGENT;
BENZYLOXYCARBONYLISOLEUCYLGLUTAMYLTHREONYLASPARTIC ACID FLUOROMETHYL KETONE;
BENZYLOXYCARBONYLVALYLALANYLASPARTYL FLUOROMETHYL KETONE;
CASPASE;
CYCLOHEXIMIDE;
DACTINOMYCIN;
DAUNORUBICIN;
DNA FRAGMENT;
ENDONUCLEASE;
ETHYL 3 [N (3 BROMO 1,4,5,8 TETRAOXO 9,10 DIHYDRO 9,10 [1',2']BENZENOANTHRACEN 2 YL)]AMINOPROPANOATE;
TERT BUTYL 3 [N (3 BROMO 1,4,5,8 TETRAOXO 9,10 DIHYDRO 9,10 [1',2']BENZENOANTHRACEN 2 YL)]AMINOPROPANOATE;
TOSYLPHENYLALANYL CHLOROMETHYL KETONE;
TRIPTYCENE DERIVATIVE;
UNCLASSIFIED DRUG;
ZINC SULFATE;
6 BROMO 7 METHOXY 2 N METHYLAMINO 1H,4H,5H,8H 9,10 DIHYDRO 9,10 (1',2')BENZENOANTHRACENE 1,4,5,8 TETRAONE;
6-BROMO-7-METHOXY-2-N-METHYLAMINO-1H,4H,5H,8H-9,10-DIHYDRO-9,10-(1',2')BENZENOANTHRACENE-1,4,5,8-TETRAONE;
7 BROMO 6 METHOXY 2 N METHYLAMINO 1H,4H,5H,8H 9,10 DIHYDRO 9,10 (1',2')BENZENOANTHRACENE 1,4,5,8 TETRAONE;
7-BROMO-6-METHOXY-2-N-METHYLAMINO-1H,4H,5H,8H-9,10-DIHYDRO-9,10-(1',2')BENZENOANTHRACENE-1,4,5,8-TETRAONE;
ANTHRAQUINONE DERIVATIVE;
ANTINEOPLASTIC AGENT;
ANTINEOPLASTIC ANTIBIOTIC;
BRIDGED COMPOUND;
DNA;
NUCLEOSIDE;
ANIMAL CELL;
ANTINEOPLASTIC ACTIVITY;
APOPTOSIS;
ARTICLE;
CELL VIABILITY;
CHROMATIN CONDENSATION;
COMBINATION CHEMOTHERAPY;
CONCENTRATION RESPONSE;
CONTROLLED STUDY;
CYTOTOXICITY;
DNA CLEAVAGE;
DNA DAMAGE;
DRUG POTENCY;
ENZYME ACTIVATION;
IN VITRO STUDY;
LEUKEMIA L 1210;
MULTIDRUG RESISTANCE;
NONHUMAN;
NUCLEOSIDE TRANSPORT;
PRIORITY JOURNAL;
ANIMAL;
BIOSYNTHESIS;
CELL SURVIVAL;
DRUG EFFECT;
HUMAN;
METABOLISM;
ANIMAL;
ANTHRAQUINONES;
ANTIBIOTICS, ANTHRACYCLINE;
ANTINEOPLASTIC AGENTS;
APOPTOSIS;
BRIDGED COMPOUNDS;
CELL SURVIVAL;
DAUNORUBICIN;
DNA FRAGMENTATION;
DNA, NEOPLASM;
HUMAN;
LEUKEMIA L1210;
NUCLEOSIDES;
SUPPORT, NON-U.S. GOV'T;
SUPPORT, U.S. GOV'T, NON-P.H.S.;
SUPPORT, U.S. GOV'T, P.H.S.;
ANIMALS;
ANTIBIOTICS, ANTINEOPLASTIC;
HUMANS;
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EID: 0036021016
PISSN: 09594973
EISSN: None
Source Type: Journal
DOI: 10.1097/00001813-200207000-00003 Document Type: Article |
Times cited : (20)
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References (50)
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