Abstract

A series of isatin-3-arylhydrazones were synthesized and evaluated in vitro as inhibitors of Ab1-40 aggregation using a thioflavin T fluorescence method. An exploration of the effects on Ab1-40 aggregation of a number of diverse substituents at phenylhydrazone group and 5,6- positions of the indolinone nucleus led us to single out some new anti-aggregating compounds with IC50 values in the low micromolar range. The most active compounds carry methoxy- or hydroxy- substituents in the indolinone 5,6-positions and lipophilic groups such as iPr and Cl at 40- and 30-position, respectively, of the phenylhydrazone moiety. Two derivatives are noteworthy, namely 18 (IC50 = 0.4 mM) and 42 (IC50 = 1.1 mM). The in vitro effects of the highly active, water soluble, compound 42 on the temporal evolution of Ab1-40 fibrils formation were further investigated by circular dichroism spectroscopy, transmission electron microscopy and dynamic light scattering studies, which clearly showed that this compound delayed and lowered the amyloid fibril formation

Autore Pugliese

• De Stradis Angelo

Tutti gli autori

• Campagna F.; Catto M.; Purgatorio R.; Altomare C.D.; Carotti A.; De Stradis A.; Palazzo G.

Titolo volume/Rivista

European journal of medicinal chemistry

Anno di pubblicazione

2011

ISSN

0223-5234

ISBN

Non Disponibile

Numero di citazioni Wos

Nessuna citazione

Ultimo Aggiornamento Citazioni

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Numero di citazioni Scopus

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Ultimo Aggiornamento Citazioni

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Settori ERC

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Codici ASJC

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