Two triaryl-3(2H)-furanones were synthesized and their antitumor activity was evaluated. These compounds inhibited the proliferation of DLA cell line in vitro. In vivo studies also showed that these compounds were active against tumor cell proliferation. (C) 2008 Elsevier Ltd. All rights reserved.
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UNIV ROME LA SAPIENZA,DEPARTIMENTO CHIM,CNR,CTR STUDIO CHIM SOSTANZE ORGAN NAT,P A MORO 5,I-00185 ROME,ITALYUNIV ROME LA SAPIENZA,DEPARTIMENTO CHIM,CNR,CTR STUDIO CHIM SOSTANZE ORGAN NAT,P A MORO 5,I-00185 ROME,ITALY
ANTONIOLETTI, R
BONADIES, F
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UNIV ROME LA SAPIENZA,DEPARTIMENTO CHIM,CNR,CTR STUDIO CHIM SOSTANZE ORGAN NAT,P A MORO 5,I-00185 ROME,ITALYUNIV ROME LA SAPIENZA,DEPARTIMENTO CHIM,CNR,CTR STUDIO CHIM SOSTANZE ORGAN NAT,P A MORO 5,I-00185 ROME,ITALY
BONADIES, F
SCETTRI, A
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UNIV ROME LA SAPIENZA,DEPARTIMENTO CHIM,CNR,CTR STUDIO CHIM SOSTANZE ORGAN NAT,P A MORO 5,I-00185 ROME,ITALYUNIV ROME LA SAPIENZA,DEPARTIMENTO CHIM,CNR,CTR STUDIO CHIM SOSTANZE ORGAN NAT,P A MORO 5,I-00185 ROME,ITALY