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Synthesis of biliverdin and bilirubin 1-O-acyl-beta-D-glucopyranuronic acids.

ABSTRACT: Biliverdin and bilirubin mono- and di-beta-glucuronides were prepared by nucleophilic substitution of the 1-O-mesyl derivative of alpha-ethoxyethyl-protected glucuronic acid (compound II) with the tetrabutylammonium salts of biliverdin and bilirubin. Removal of the acetal-protecting groups by mild acid treatment yielded biliverdin glucuronides, which were reduced to bilirubin glucuronides. Depending on reaction conditions the pure beta-anomers or mixtures highly enriched in the beta-anomers were obtained. The biliverdin and bilirubin glucuronides were identical with pigments derived from bile. They were characterized as the IX alpha isomers and the beta-anomers by alkaline hydrolysis, n.m.r. spectroscopy, hydrolysis with beta-glucuronidase and conversion into dipyrrolic azopigments. Model reactions of the 1-O-mesylate (II) with other nucleophiles also were performed, i.e. the acetate anion and various alcohols.

SUBMITTER: Compernolle F

PROVIDER: S-EPMC1162472 | biostudies-other | 1980 Jun

REPOSITORIES: biostudies-other

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Unprecedented Microbial Conversion of Biliverdin into Bilirubin-10-sulfonate.

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