Skip to Content
Merck
  • Cytotoxic effect and molecular docking of 4-ethoxycarbonylmethyl-1-(piperidin-4-ylcarbonyl)-thiosemicarbazide--a novel topoisomerase II inhibitor.

Cytotoxic effect and molecular docking of 4-ethoxycarbonylmethyl-1-(piperidin-4-ylcarbonyl)-thiosemicarbazide--a novel topoisomerase II inhibitor.

Journal of molecular modeling (2012-11-29)
Agata Siwek, Paweł Stączek, Monika Wujec, Krzysztof Bielawski, Anna Bielawska, Piotr Paneth
ABSTRACT

The preliminary cytotoxic effect of 4-ethoxycarbonylmethyl-1-(piperidin-4-ylcarbonyl)-thiosemicarbazide hydrochloride (1)-a potent topoisomerase II inhibitor-was measured using a MTT assay. It was found that the compound decreased the number of viable cells in both estrogen receptor-positive MCF-7 and estrogen receptor-negative MDA-MB-231breast cancer cells, with IC(50) values of 146 ± 2 and 132 ± 2 μM, respectively. To clarify the molecular basis of the inhibitory action of 1, molecular docking studies were carried out. The results suggest that 1 targets the ATP binding pocket.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Thiosemicarbazide, 99%
Sigma-Aldrich
Thiosemicarbazide, puriss. p.a., 98%