hyodeoxycholic-acid and squalamine

Analogs of the aminosterol antimicrobial agent squalamine have been synthesized beginning from hyodeoxycholic acid. After carboxylic acid esterification and oxidation of both alcohol functions to ketones, the A/B ring junction was converted from cis to trans by acid-catalyzed isomerization. Different polyamines were added to the 3-keto group by reductive amination, yielding both the 3 alpha and 3 beta addition products. The synthetic products exhibited potent, broad-spectrum antimicrobial activity similar to that of the parent compound. Changing the identity of the polyamine or the stereochemistry of addition has little effect upon antimicrobial activity but appears to change the selectivity of the agents. The analogs are synthesized with high yield from inexpensive starting materials and are promising alternatives to squalamine as potential antibiotics.

Topics: Anti-Bacterial Agents; Cholestanols; Cholic Acids; Deoxycholic Acid; Detergents; Ethylenediamines; Microbial Sensitivity Tests; Pseudomonas aeruginosa; Spermine; Staphylococcus aureus; Structure-Activity Relationship