Secondary metabolites glucuronide conjugates

The most significant metabolite of letrozole (3) is its secondary alcohol metabolite (SAM) 23 (Scheme 3.4). Biotransformation of letrozole is the main elimination mechanism, with the glucuronide conjugate of the secondary alcohol metabolite (24) being the prominent species found in urine. However, the total body clearance of letrozole is slow (2.21 L/h). Its elimination half-life is long, at 42 h. Letrozole and its metabolites are excreted mainly via the kidneys. 

Three new monoterpenoid lactones, (28)—(30), isolated from the urine of koala bears fed on Eucalyptus punctata, appear to have arisen from the cyclization of carboxylic acids formed as hydrolysis products of glucuronide conjugates from the metabolism of a- and /3-pinenes.70 Linalool injected into various plant species has been claimed to be converted into a-terpineol and other monoterpenoids.71 However, direct interconversions cannot be inferred from this type of non-radioactive tracer study. The terpenoids alleged to be produced may well be stress metabolites or be formed b secondary processes that perturb the usual pattern of terpenoid formation. 

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