Date published: 2026-4-27

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Topo II Inhibitors

Santa Cruz Biotechnology now offers a broad range of Topo II Inhibitors for use in various applications. Topo II Inhibitors are a class of compounds that target the enzyme topoisomerase II, a crucial player in DNA replication and transcription. By inhibiting this enzyme, these compounds interfere with the topological state of DNA, preventing the unwinding and rewinding processes essential for various cellular functions. In scientific research, Topo II Inhibitors are invaluable tools for studying cell cycle regulation, gene expression, and the mechanisms underlying DNA damage and repair. Researchers utilize these inhibitors to dissect the roles of topoisomerase II in chromosomal condensation, segregation, and the maintenance of genomic stability. Additionally, these compounds are used in genetic studies to induce mutations and investigate DNA-protein interactions, providing insights into fundamental biological processes. Topo II Inhibitors also serve as probes in biochemical assays to explore the dynamics of DNA topoisomerases and their interactions with other cellular components. Their application extends to biotechnology fields, where they aid in the development of new methodologies for DNA manipulation and analysis. View detailed information on our available Topo II Inhibitors by clicking on the product name.

Items 61 to 64 of 64 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Bis(cyclopentadienyl)vanadium(IV) dichloride

12083-48-6sc-227388
1 g
$58.00
(0)

Bis(cyclopentadienyl)vanadium(IV) dichloride exhibits unique interactions with topoisomerase II through its metal-centered coordination, which influences the enzyme's conformational dynamics. The compound's distinct ligand environment facilitates specific binding to the enzyme, altering its catalytic pathways. This results in a modulation of DNA supercoiling and strand passage, as the vanadium center introduces unique electronic properties that affect reaction kinetics and enzyme stability, ultimately impacting DNA topology.

Protocatechuic acid ethyl ester

3943-89-3sc-236496
5 g
$32.00
(0)

Protocatechuic acid ethyl ester engages with topoisomerase II through its aromatic structure, which enhances π-π stacking interactions with the enzyme's active site. This compound's ethyl ester moiety contributes to hydrophobic interactions, promoting a favorable binding affinity. The presence of hydroxyl groups allows for hydrogen bonding, influencing the enzyme's conformational state and catalytic efficiency, thereby modulating DNA relaxation and torsional strain during replication processes.

Sobuzoxane

98631-95-9sc-215862
sc-215862A
sc-215862B
sc-215862C
5 mg
25 mg
50 mg
100 mg
$255.00
$918.00
$1530.00
$2856.00
1
(0)

Sobuzoxane exhibits unique interactions with topoisomerase II, primarily through its ability to form stable complexes via electrostatic and hydrophobic interactions. Its structural features facilitate the disruption of the enzyme's catalytic cycle, leading to the stabilization of DNA cleavage complexes. The compound's specific conformational flexibility allows it to adapt to the enzyme's active site, influencing reaction kinetics and altering the dynamics of DNA topology during replication and repair processes.

Fostriecin

87860-39-7sc-202160
50 µg
$265.00
9
(1)

Fostriecin interacts with topoisomerase II by forming transient complexes that modulate the enzyme's activity. Its unique binding affinity stems from specific hydrogen bonding and van der Waals interactions, which enhance the stabilization of the enzyme-DNA complex. This compound also exhibits a distinctive ability to alter the conformational state of topoisomerase II, impacting the enzyme's catalytic efficiency and influencing the resolution of DNA supercoiling during cellular processes.