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Synthesis and DNA binding properties of C3-, C12-, and C24-substituted amino-steroids derived from bile acids
H P Hsieh1, J G Muller, C J Burrows
1Department of Chemistry, State University of New York, Stony Brook 11794-3400, USA.
Bioorganic & Medicinal Chemistry
|June 1, 1995
Abstract:
Seven new amino- and guanidino-substituted steroids have been synthesized from bile acid precursors, either deoxycholic acid or lithocholic acid. Their DNA binding properties have been examined using an ethidium displacement assay, through studies of hyperchromicity and thermal denaturation, and by circular dichroism. Comparison is made to simple aliphatic polyamines such as putrescine, 1,12-diaminododecane, spermidine, and spermine.