2010
DOI: 10.1016/j.jinorgbio.2010.01.010
|View full text |Cite
|
Sign up to set email alerts
|

Effect of ancillary ligands on the topoisomerases II and transcription inhibition activity of polypyridyl ruthenium(II) complexes

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1

Citation Types

1
7
0

Year Published

2010
2010
2024
2024

Publication Types

Select...
9

Relationship

3
6

Authors

Journals

citations
Cited by 35 publications
(11 citation statements)
references
References 58 publications
1
7
0
Order By: Relevance
“…The HOMO has the poorest correlation with the binding activities of the ligands which range from 0.00 to 0.18. The better correlation of the LUMO with the receptor interactions further supports the hypothesis that the lower the LUMO energy of inhibitors the easier the overlapping of it with the HOMO of the DNA [ 54 ]. However, other factors like the hydrophobicity and electronic effect of the ligands play significant roles in their inhibitory activities [ 54 ].…”
Section: Resultssupporting
confidence: 52%
“…The HOMO has the poorest correlation with the binding activities of the ligands which range from 0.00 to 0.18. The better correlation of the LUMO with the receptor interactions further supports the hypothesis that the lower the LUMO energy of inhibitors the easier the overlapping of it with the HOMO of the DNA [ 54 ]. However, other factors like the hydrophobicity and electronic effect of the ligands play significant roles in their inhibitory activities [ 54 ].…”
Section: Resultssupporting
confidence: 52%
“…Investigation of new complexes by using various metals and ligands is necessary to understand role and importance of the effect factors on the medicinal properties. The effect of ancillary ligands on the biological and anticancer activity of polypyridyl complexes has also been examined [20,21]. It is found that ancillary ligands with the higher planarity and hydrophobicity are beneficial in biological and anticancer activity of their complexes.…”
Section: Introductionmentioning
confidence: 99%
“…Moreover, the structure of its active site is similar to that of other viral, bacterial and eukaryotic polymerases [5,6]. T7 RNAP is thus a reliable in vitro model used for the studies of transcription [3][4][5][6] and mechanism of action of DNAbinding drugs [7][8][9][10]. This system was proposed in our previous papers for the screening of nucleic acids synthesis inhibitors [11][12][13].…”
Section: Introductionmentioning
confidence: 99%