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It is formed when squalene is oxidized by the enzyme squalene monooxygenase. 2,3-Oxidosqualene is the substrate of various oxidosqualene cyclases, including lanosterol synthase, which produces lanosterol, a precursor to cholesterol. [1] The stereoisomer (R)-2,3-oxidosqualene is an inhibitor of lanosterol synthase.
Lanosterol is a tetracyclic triterpenoid and is the compound from which all animal and fungal steroids are derived. By contrast, plant steroids are produced via cycloartenol . [ 1 ] In the eyes of vertebrates, lanosterol is a natural constituent, having a role in maintaining health of the lens .
Research is being done for other compounds which block different steps in the biosynthesis of cholesterol, including the reaction performed by oxidosqualene cyclase which cyclizes squalene to form lanosterol. [7] Oxidosqualene cyclase, which is downstream of squalene in the pathway, is an attractive target for inhibition.
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Lanosterol synthase (EC 5.4.99.7) is an oxidosqualene cyclase (OSC) enzyme that converts -2,3-oxidosqualene to a protosterol cation and finally to lanosterol. [5] Lanosterol is a key four-ringed intermediate in cholesterol biosynthesis.
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