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Synthesis and cytotoxicity of bis(benzo[g]indole-3-carboxamides) and related compounds

Pinna, Gérard Aimé and Pirisi, Maria Antonietta and Grella, Giuseppe Enrico and Gherardini, Laura and Mussinu, Jean-Mario and Paglietti, Giuseppe and Ferrari, Anna M. and Rastelli, Giulio (2001) Synthesis and cytotoxicity of bis(benzo[g]indole-3-carboxamides) and related compounds. Archiv der Pharmazie, Vol. 334 (11), p. 337-344. eISSN 1521-4184. Article.

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DOI: 10.1002/1521-4184(200112)334:11<337::AID-ARDP337>3.0.CO;2-Y


A series of bis(benzo[g]indoles) bridged by CX-(CH2)nN(Me)(CH2)n-CX (X = O, S, H2; n = 2,3) was synthesized as bifunctional antitumor agents and evaluated for cytotoxic activity against diverse human cancer cell lines by the National Cancer Institute. The parent compounds 2a,b exhibited a good level of activity and derivates 2c - g,i,k demonstrated significant inhibitory effects, all with IC50 values in the low micromolar range. The thioamide analogue 2j showed less potency. It is interesting to note that introduction of substituents on the benzene ring of the benzo[g]indole portion of 2a,b did not affect activity, with the only exception of the 7,8-dichloro derivative 2h which became less potent. One member of this series, 2i, was then tested in the hollow fiber cell assay to evaluate, in a preliminary fashion, its in vivo antineoplastic activity. Molecular modelling studies were performed on amide 2a and thioamide 2j to explain the loss of activity of 2j as to 2a. Finally, compound 2a behaved as a typical DNAintercalating agent, as judged from viscosity measurements with Poly(dA-dT) .. poly(dA-dT).

Item Type:Article
ID Code:555
Uncontrolled Keywords:Cytotoxic activity (IC50), bisbenzo[g]indoles, SAR studies, modelling, viscosity
Subjects:Area 03 - Scienze chimiche > CHIM/08 Chimica farmaceutica
Divisions:001 Università di Sassari > 01 Dipartimenti > Farmaco, chimico, tossicologico
Deposited On:18 Aug 2009 10:02

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