Though first isolated in the 1960s, there has been very little investigation of the
biosynthetic pathway of catalpol. Addition of a glucose at carbon 1 (C1) of the iridoid backbone and oxidation of the aldehyde at C4 of epi-iridotrial produces 8-epiloganic acid. A subsequent hydrolysis at C8 yields mussaenosidic acid, followed by a dehydration to yield deoxyngeniposidic acid. The next precursor,
geniposidic acid, is furnished via hydrolysis of C10, and then a decarboxylation to remove the carboxylic acid at C4 provides bartsioside. The very widely known and accepted precursor to catalpol,
aucubin, is then furnished via hydroxylation at C6. Finally an epoxidation with the alcohol at C10 yields catalpol. == Footnotes ==