European Journal of Medicinal Chemistry p. 43 - 46 (1998)
Update date:2022-09-26
Topics:
Garuti, Laura
Roberti, Marinella
Rossi, Tiziana
Castelli, Mario
Malagoli, Monica
Some 3-substituted indole-triazin-4-ones were synthesized. Their antiproliferative activity against chronic myeloid leukaemia and non-Hodgkin lymphoma human cells was compared in vitro with that of daunorubicin. One compound appeared to be very effective against human CML.
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