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Bioelectrochemistry ; 69(1): 1-9, 2006 Sep.
Article in English | MEDLINE | ID: mdl-16307909

ABSTRACT

Facile and practical electrochemical DNA bioassay, X-ray diffraction analysis, synthesis and 1H and 13C NMR data of the 5,5'-disubstituted-3,3'-methanediyl-bis-indoles are reported. On the basis of electrochemical measurements we have hypothesized that the analyzed bis-indoles have an effect on human tumor cells due to DNA binding at adenine-thymidine deoxynucleotides rich region in a concentration/substituent dependent manner. Interesting N-H...pi and hydrogen-bonding intermolecular interactions were observed which may differentiate their biological features. The 5,5'-dimethoxy-3,3'-methanediyl-bis-indole (2) was found to reduce considerably the growth of cancer cell lines HOP-92 (lung), A498 (renal) and MDA-MB-231/1TCC (breast). The results indicate that title compounds could be interesting as potential antitumoral chemotherapeutics.


Subject(s)
Antineoplastic Agents/chemistry , Biosensing Techniques/methods , DNA/chemistry , Indoles/chemistry , Antineoplastic Agents/chemical synthesis , Antineoplastic Agents/pharmacology , Cell Line, Tumor , Cell Proliferation/drug effects , Crystallography, X-Ray , Drug Screening Assays, Antitumor , Electrochemistry , Humans , Hydrogen Bonding , Indoles/chemical synthesis , Indoles/pharmacology , Magnetic Resonance Spectroscopy , Models, Molecular , Molecular Structure , Sensitivity and Specificity , X-Ray Diffraction
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