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Volumn 28, Issue 6, 2005, Pages 1004-1009
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Synthesis, DNA binding, topoisomerase inhibition and cytotoxic properties of 2-chloroethylnitrosourea derivatives of Hoechst 33258
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Author keywords
Chloroethylnitrosourea; Cytotoxicity; DNA topoisomerase; DNA binding; Hoechst 33258; Ultrafiltration assay
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Indexed keywords
2 CHLOROETHYLNITROSOUREA DERIVATIVE;
4 [5 (4 METHYL 1 PIPERAZINYL)[2,5' BI 1H BENZIMIDAZOL] 2' YL]PHENOL;
4 [6 [5 (4 METHYLPIPERAZIN 1 YL)BENZIMIDAZOL 2 YL]BENZIMIDAZOL 2 YL]PHENYL 2 [2 [3 (2 CHLOROETHYL) 3 NITROSOUREIDO] 3 METHYLBUTANAMIDO]ETHYL CARBAMATE;
4 [6 [5 (4 METHYLPIPERAZIN 1 YL)BENZIMIDAZOL 2 YL]BENZIMIDAZOL 2 YL]PHENYL 2 [2 [3 (2 CHLOROETHYL) 3 NITROSOUREIDO]ACETAMIDO]ETHYL CARBAMATE;
4 [6 [5 (4 METHYLPIPERAZIN 1 YL)BENZIMIDAZOL 2 YL]BENZIMIDAZOL 2 YL]PHENYL 2 [2 [3 (2 CHLOROETHYL) 3 NITROSOUREIDO]PROPANAMIDO]ETHYL CARBAMATE;
DEOXYRIBONUCLEOTIDE;
DNA TOPOISOMERASE;
DNA TOPOISOMERASE (ATP HYDROLYSING);
DNA TOPOISOMERASE INHIBITOR;
DOUBLE STRANDED DNA;
NITROSOUREA DERIVATIVE;
POLY(DEOXYADENYLATE DEOXYTHYMIDYLATE);
UNCLASSIFIED DRUG;
ARTICLE;
BASE PAIRING;
BINDING AFFINITY;
BREAST CANCER;
CANCER CELL CULTURE;
CANCER INHIBITION;
CARBON NUCLEAR MAGNETIC RESONANCE;
CELL PROLIFERATION;
CELL STRAIN MCF 7;
CELL STRAIN MDA MB 231;
CELL VIABILITY;
CONTROLLED STUDY;
DNA SYNTHESIS;
DRUG CYTOTOXICITY;
DRUG DNA BINDING;
DRUG MECHANISM;
DRUG SYNTHESIS;
ENZYME INHIBITION;
HUMAN;
HUMAN CELL;
MELTING POINT;
PROTON NUCLEAR MAGNETIC RESONANCE;
ULTRAFILTRATION;
ANIMALS;
BISBENZIMIDE;
CATTLE;
CELL LINE, TUMOR;
DNA;
DNA TOPOISOMERASES;
ENZYME INHIBITORS;
HUMANS;
NITROSOUREA COMPOUNDS;
PROTEIN BINDING;
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EID: 21144439018
PISSN: 09186158
EISSN: None
Source Type: Journal
DOI: 10.1248/bpb.28.1004 Document Type: Article |
Times cited : (25)
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References (25)
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