| Autor: |
M F, Braña, J M, Castellano, M, Morán, M J, Pérez de Vega, D, Perron, D, Conlon, P F, Bousquet, C A, Romerdahl, S P, Robinson |
| Rok vydání: |
1996 |
| Předmět: |
|
| Zdroj: |
Anti-cancer drug design. 11(4) |
| ISSN: |
0266-9536 |
| Popis: |
The bis-naphthalimides are a new class of antitumor agent. Previously, we have described initial synthetic series which established that two naphthalimide chromophores joined by polyamine linkers can produce agents with antitumor activity. We now extend these studies to describe the synthesis of a N,N'-bis[1,8-naphthalimido)-ethyl]alkanediamine series and examine the alkyl linker and chromophore substitution requirements for optimal antitumor activity. As a result, a bis-naphthal-imidoethyl derivative with no chromophore substitution and a NH-(CH2)3-NH bridge was identified. This agent (LU 79553) had both potent cellular cytotoxicity (IC50 = 0.014 microM) and was curative against MX-1 tumors grown in athymic mice. It has now been selected for clinical development. |
| Databáze: |
OpenAIRE |
| Externí odkaz: |
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