Davey, R.A., et al., The potential of N-[2-(dimethylamino)ethyl]acridine-4-carboxamide to circumvent three multidrug-resistance phenotypes in vitro. Cancer Chemother. Pharmacol. 39, 424-430, (1997) Nelson, E.M., et al., Mechanism of antitumor drug action: poisoning of mammalian DNA topoisomerase II on DNA by 4'-(9-acridinylamino)-methanesulfon-m-anisidide. Proc. Natl. Acad. Sci. USA 81, 1361-1365, (1984) Ferguson, L.R., , Application of fluorescence in situ hybridization to study the relationship between cytotoxicity, chromosome aberrations, and changes in chromosome number after treatment with the topoisomerase II inhibitor amsacrine. Environ. Mol. Mutagen. 27, 255, (1996) Mosesso, P., et al., Induction of chromosomal aberrations (unstable and stable) by inhibitors of topoisomerase II, m-AMSA and VP16, using conventional Giemsa staining and chromosome painting techniques. Mutagenesis 13, 39-43, (1998) Del Bino, G., et al., The concentration-dependent diversity of effects of DNA topoisomerase I and II inhibitors on the cell cycle of HL-60 cells. Exp. Cell Res. 195, 485-491, (1991) Negri, C., et al., Induction of apoptotic cell death by DNA topoisomerase II inhibitors. Biochimie 77, 893-899, (1995)
Inhibitor of:
4930547C10Rik, AI481877, Borealin, C6orf167, CENP-L, DDX10, DDX19B, DDX42, DDX52, DFF-45, DNA pol 4, ds DNA Marker, ENSMUSG00000073257, FIGNL2, GEN1, hCAP-H, Hfm1, HTH, Mad 4, MsrB3, Ncapg, Nop5, OBFC2B, OFCC1, PIF1, PMS2, Rec8, RPA40, SNM1A, SSBP2, SWAP, THAP9, Topo II, Topo IIIβ, UIMC1, and ZNF154.
Activator of:
4930547C10Rik, ALKBH2, AROS-29, TDP2, Top1, and Top3.
Appearance :
Powder
Physical State :
Solid
Solubility :
Soluble in DMSO: 10 mg/mL with heat and sonication and 30% Ethanol: 4 mg/mL
Storage :
Store at room temperature
Melting Point :
197-199° C (lit.)
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
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