Novel iodoacetamido benzoheterocyclic derivatives with potent antileukemic activity are inhibitors of STAT5 phosphorylation

Stefania Grimaudo, Rosaria Maria Pipitone, Maria Meli, Carlota Lopez-Cara, Ernest Hamel, Filippo Prencipe, Riccardo Rondanin, Daniele Simoni, Pier Giovanni Baraldi, Romeo Romagnoli, Daniele Simoni

Risultato della ricerca: Article

4 Citazioni (Scopus)

Abstract

Signal Transducer and Activator of Transcription 5 (STAT5) protein, a component of the STAT family of signaling proteins, is considered to be an attractive therapeutic target because of its involvement in the progression of acute myeloid leukemia. In an effort to discover potent molecules able to inhibit the phosphorylation-activation of STAT5, twenty-two compounds were synthesized and evaluated on the basis of our knowledge of the activity of 2-(3′,4′,5′-trimethoxybenzoyl)-3-iodoacetamido-6-methoxy benzo[b]furan derivative 1 as a potent STAT5 inhibitor. Most of these molecules, structurally related to compound 1, were characterized by the presence of a common 3′,4′,5′-trimethoxybenzoyl moiety at the 2-position of different benzoheterocycles such as benzo[b]furan, benzo[b]thiophene, indole and N-methylindole. Effects on biological activity of the iodoacetamido group and of different moieties (methyl and methoxy) at the C-3 to C-7 positions were examined. In the series of benzo[b]furan derivatives, moving the iodoacetylamino group from the C-4 to the C-5 or C-6 positions did not significantly affect antiproliferative activity. Compounds 4, 15, 20 and 23 blocked STAT5 signals and induced apoptosis of K562 BCR-ABL positive cells. For compound 23, the trimethoxybenzoyl moiety at the 2-position of the benzo[b]furan core was not essential for potent inhibition of STAT5 activation.
Lingua originaleEnglish
pagine (da-a)39-52
Numero di pagine14
RivistaEuropean Journal of Medicinal Chemistry
Volume108
Stato di pubblicazionePublished - 2016

    Fingerprint

All Science Journal Classification (ASJC) codes

  • Pharmacology
  • Drug Discovery
  • Organic Chemistry

Cita questo

Grimaudo, S., Pipitone, R. M., Meli, M., Lopez-Cara, C., Hamel, E., Prencipe, F., Rondanin, R., Simoni, D., Baraldi, P. G., Romagnoli, R., & Simoni, D. (2016). Novel iodoacetamido benzoheterocyclic derivatives with potent antileukemic activity are inhibitors of STAT5 phosphorylation. European Journal of Medicinal Chemistry, 108, 39-52.