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Volumn 16, Issue 8, 2008, Pages 4545-4550
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Synthesis of 1-/2-substituted-[1,2,3]triazolo[4,5-g]phthalazine-4,9-diones and evaluation of their cytotoxicity and topoisomerase II inhibition
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Author keywords
Cytotoxicity; Topoisomerase II; Triazolophthalazine
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Indexed keywords
1 ETHYL 1H [1,2,3]TRIAZOLO[4,5 G]PHTHALAZINE 4,9 DIONE;
1 ISO BUTYL L 1H [1,2,3]TRIAZOLO[4,5 G]PHTHALAZINE 4,9 DIONE;
1 ISO PROPYL L 1H [1,2,3]TRIAZOLO[4,5 G]PHTHALAZINE 4,9 DIONE;
1 METHYL 1H [1,2,3]TRIAZOLO[4,5 G]PHTHALAZINE 4,9 DIONE;
1 N BUTYL 1H [1,2,3]TRIAZOLO[4,5 G]PHTHALAZINE 4,9 DIONE;
1 N PROPYL 1H [1,2,3]TRIAZOLO[4,5 G]PHTHALAZINE 4,9 DIONE;
2 ETHYL 1H [1,2,3]TRIAZOLO[4,5 G]PHTHALAZINE 4,9 DIONE;
2 ISO BUTYL L 1H [1,2,3]TRIAZOLO[4,5 G]PHTHALAZINE 4,9 DIONE;
2 ISO PROPYL L 1H [1,2,3]TRIAZOLO[4,5 G]PHTHALAZINE 4,9 DIONE;
2 METHYL 1H [1,2,3]TRIAZOLO[4,5 G]PHTHALAZINE 4,9 DIONE;
2 N BUTYL 1H [1,2,3]TRIAZOLO[4,5 G]PHTHALAZINE 4,9 DIONE;
2 N PROPYL 1H [1,2,3]TRIAZOLO[4,5 G]PHTHALAZINE 4,9 DIONE;
ANTINEOPLASTIC AGENT;
DNA TOPOISOMERASE (ATP HYDROLYSING);
DOXORUBICIN;
ETOPOSIDE;
QUINONE DERIVATIVE;
SULFORHODAMINE B;
UNCLASSIFIED DRUG;
ADDITION REACTION;
ANTINEOPLASTIC ACTIVITY;
ARTICLE;
CANCER CELL CULTURE;
CONTROLLED STUDY;
CYTOTOXICITY;
DRUG ACTIVITY;
DRUG DETERMINATION;
DRUG STRUCTURE;
DRUG SYNTHESIS;
ENZYME INHIBITION;
HUMAN;
HUMAN CELL;
AZO COMPOUNDS;
BENZOQUINONES;
CELL LINE, TUMOR;
CELL SURVIVAL;
DNA TOPOISOMERASES, TYPE II;
HUMANS;
MOLECULAR STRUCTURE;
PHTHALAZINES;
RHODAMINES;
STRUCTURE-ACTIVITY RELATIONSHIP;
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EID: 42149176832
PISSN: 09680896
EISSN: None
Source Type: Journal
DOI: 10.1016/j.bmc.2008.02.049 Document Type: Article |
Times cited : (75)
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References (22)
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