Dp44mT

本公司产品仅用于科研实验，不得用于人体或动物的临床与诊断

Dp44mT 是一种有效的铁螯合剂，具有选择性抗肿瘤活性。

Dp44mT is an iron chelator, possessing DNA-damaging activity mediated by top2a inhibition.

Dp44mT is cytotoxic to breast cancer cells, at least in part, due to selective inhibition of top2α. Dp44mT alone induced selective cell killing in the breast cancer cell line MDA-MB-231 when compared with healthy mammary epithelial cells (MCF-12A). It induces G1 cell cycle arrest and reduces cancer cell clonogenic growth at nanomolar concentrations. Dp44mT, but not the iron chelator desferal, induces DNA double-strand breaks quantified as S139 phosphorylated histone foci (γ-H2AX) and Comet tails induced in MDA-MB-231 cells. Doxorubicin-induced cytotoxicity and DNA damage are both enhanced significantly in the presence of low concentrations of Dp44mT. The chelator caused selective poisoning of DNA topoisomerase IIα (top2α) as measured by an in vitro DNA cleavage assay and cellular topoisomerase-DNA complex formation. Dp44mT targets lysosome integrity through copper binding. Copper binding is essential for the potent antitumor activity of Dp44mT, as coincubation with nontoxic copper chelators markedly attenuated its cytotoxicity.

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Dp44mT

Autophagy

SIK

iron chelator

Others-Field

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152095-12-0

285.37

C14H15N5S

>98% (HPLC)

DMSO : 100 mg/mL 350.42 mM;

CN(C)C(=S)NN=C(c1ccccn1)c1ncccc1

3-(Dipyridin-2-ylmethylideneamino)-1,1-dimethylthiourea

(-20℃)

With Ice Pack

≥ 2 years