<p>(A) Connectivity Map (CMAP) results after treatment with thaspine. The bar view is constructed from 6100 horizontal lines, each representing a single treatment and ordered according to their corresponding enrichment to the query signatures generated after thaspine treatment. Black horizontal lines in the barview represent the individual instances for ellipticine and camptothecin when the thaspine expression signature was used as query signature. Score according to the CMAP database; (B) inhibition of topoisomerase I activity: 1: plasmid +5U topoisomerase I; 2: plasmid; 3: plasmid +5U topoisomerase I+DMSO (1 µm); 4. Marker for nicked plasmid; 5: plasmid +5U topoisomerase I +50 µM thaspine; 6: plasmid +5U topoisomerase I +25 µM thaspine; 7...
Human topoisomerase I (Top1) plays a pivotal role in cell replication and transcription, and therefo...
Computer Aided Drug Discovery (CADD) is a broad field which uses scientific tools from various dispa...
<p>Amsacrine, which inhibits eukaryotic type II topoisomerase via DNA intercalation and stabilizatio...
The different steps of the topoisomerase I catalytic cycle have been analyzed in the presence of the...
Background: Natural product structures have high chemical diversity and are attractive as lead struc...
BACKGROUND:Natural product structures have high chemical diversity and are attractive as lead struct...
Topoisomerase inhibiting chemotherapy is most appropriate in cancers containing high levels of topoi...
<p>The resistance factor was defined as the IC<sub>50</sub> value in the resistant subline divided b...
International audienceEcteinascidin 743 (Et743, National Service Center 648766) is a potent antitumo...
<p>Amsacrine, which inhibits eukaryotic type II topoisomerase via DNA intercalation and stabilizatio...
Bis-netropsins (bis-Nts) are known to be efficient inhibitors of human DNA topoisomerase (topo) I wi...
Diploid human fibroblast strains were treated for 10 min with inhibitors of type I and type II DNA t...
DNA topoisomerases are enzymes responsible for the relaxation of DNA torsional strain, as well as fo...
<p>Amsacrine, which inhibits eukaryotic type II topoisomerase via DNA intercalation and stabilizatio...
<p>Amsacrine, which inhibits eukaryotic type II topoisomerase via DNA intercalation and stabilizatio...
Human topoisomerase I (Top1) plays a pivotal role in cell replication and transcription, and therefo...
Computer Aided Drug Discovery (CADD) is a broad field which uses scientific tools from various dispa...
<p>Amsacrine, which inhibits eukaryotic type II topoisomerase via DNA intercalation and stabilizatio...
The different steps of the topoisomerase I catalytic cycle have been analyzed in the presence of the...
Background: Natural product structures have high chemical diversity and are attractive as lead struc...
BACKGROUND:Natural product structures have high chemical diversity and are attractive as lead struct...
Topoisomerase inhibiting chemotherapy is most appropriate in cancers containing high levels of topoi...
<p>The resistance factor was defined as the IC<sub>50</sub> value in the resistant subline divided b...
International audienceEcteinascidin 743 (Et743, National Service Center 648766) is a potent antitumo...
<p>Amsacrine, which inhibits eukaryotic type II topoisomerase via DNA intercalation and stabilizatio...
Bis-netropsins (bis-Nts) are known to be efficient inhibitors of human DNA topoisomerase (topo) I wi...
Diploid human fibroblast strains were treated for 10 min with inhibitors of type I and type II DNA t...
DNA topoisomerases are enzymes responsible for the relaxation of DNA torsional strain, as well as fo...
<p>Amsacrine, which inhibits eukaryotic type II topoisomerase via DNA intercalation and stabilizatio...
<p>Amsacrine, which inhibits eukaryotic type II topoisomerase via DNA intercalation and stabilizatio...
Human topoisomerase I (Top1) plays a pivotal role in cell replication and transcription, and therefo...
Computer Aided Drug Discovery (CADD) is a broad field which uses scientific tools from various dispa...
<p>Amsacrine, which inhibits eukaryotic type II topoisomerase via DNA intercalation and stabilizatio...