Resumo (PT):
The synthesis of five new tetracyclic benzopsoralen analogues, compounds 2–6, with 9H-xanthen-9-one or 9H-carbazole frameworks, is described. Their inhibitory effects on the growth of three human tumor cell lines (MCF-7, SF-268, and NCI-460) were evaluated, and discussed in terms of structure–activity relationship, taking into account both geometric and electronic features. Generally, the angular compounds showed significant biological activities, but the arrangement of functional groups also contributed to the overall activity.
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Keywords:Antitumor activity;Tumor growth inhibition;Benzopsoralen;Structure–activity relationship (SAR);Cytotoxic activity;Carbazoles;Xanthones
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<a target="_blank" href="http://onlinelibrary.wiley.com/doi/10.1002/cbdv.200790089/abstract"> Texto integral </a>
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Abstract (EN):
The synthesis of five new tetracyclic benzopsoralen analogues, compounds 2–6, with 9H-xanthen-9-one or 9H-carbazole frameworks, is described. Their inhibitory effects on the growth of three human tumor cell lines (MCF-7, SF-268, and NCI-460) were evaluated, and discussed in terms of structure–activity relationship, taking into account both geometric and electronic features. Generally, the angular compounds showed significant biological activities, but the arrangement of functional groups also contributed to the overall activity.
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Keywords:Antitumor activity;Tumor growth inhibition;Benzopsoralen;Structure–activity relationship (SAR);Cytotoxic activity;Carbazoles;Xanthones
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<a target="_blank" href="http://onlinelibrary.wiley.com/doi/10.1002/cbdv.200790089/abstract"> Full text </a>
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Language:
English
Type (Professor's evaluation):
Scientific