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Chem Biodivers ; 4(5): 980-90, 2007 May.
Article in English | MEDLINE | ID: mdl-17510993

ABSTRACT

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.


Subject(s)
Antineoplastic Agents/chemical synthesis , Antineoplastic Agents/pharmacology , Carbazoles/pharmacology , Furocoumarins/pharmacology , Antineoplastic Agents/chemistry , Carbazoles/chemical synthesis , Carbazoles/chemistry , Cell Proliferation/drug effects , Drug Screening Assays, Antitumor , Furocoumarins/chemical synthesis , Furocoumarins/chemistry , Humans , Inhibitory Concentration 50 , Structure-Activity Relationship , Tumor Cells, Cultured
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