Comparison of the cytotoxicity of amsacrine and its analogue CI-921 against cultured human and mouse bone marrow tumour cells

Author:

Ching Lai-Ming,Finlay Graeme J.,Joseph Wayne R.,Baguley Bruce C.

Publisher

Elsevier BV

Subject

Oncology

Reference26 articles.

1. The experimental antitumour properties of three congeners of the acridinyl methanesulphonanilide (AMSA) series;Cain;Eur J Cancer,1974

2. Current status of amsacrine combination chemotherapy programs in acute leukaemia;Arlin;Cancer Treat Rep,1983

3. Synthesis, antitumor activity and DNA binding properties of a new derivative of amsacrine N,5-dimethyl-9-((2-methoxy-4-methylsulfonylamino)-phenylamino)-4-acridinecarboxamide;Baguley;Cancer Res,1984

4. A multicenter assessment of the experimental antitumor activity of the amsacrine analog, CI-921;Leopold;J Natl Cancer Inst,1987

5. The clinical pharmacokinetics of N-5-dimethyl-9[(2-methoxy-4-methyl-sulfonylamino)phenylamino]-4-acridinecarboxamide (CI-921) in a phase I trial;Paxton;Cancer Chem Pharm,1988

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