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Functionalized Spirocyclic Heterocycle Synthesis and Cytotoxicity Assay
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Structure-activity relationship of N-methyl-bisindolylmaleimide derivatives as cell death inhibitors
Miho Katoh1, Kosuke Dodo, Mikako Fujita
1Institute of Multidisciplinary Research for Advanced Materials (IMRAM), Tohoku University, 2-1-1 Katahira, Aoba, Sendai, Miyagi 980-8577, Japan.
Bioorganic & Medicinal Chemistry Letters
|May 18, 2005
Abstract:
A series of N-methyl-bisindolylmaleimide derivatives was synthesized and evaluated as cell death inhibitors. N-Methyl-2-[1-(3-aminopropyl)-1H-indol-3-yl]-3-(1H-indol-3-yl)maleimide (21) was the most potent inhibitor of H2O2-induced necrotic death of human leukemia HL60 cells among them.
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