Novel results on the biocyclisation of 2,3-oxidosqualene analogs by sterol cyclase

A. Krief, P. Pasau, E. Guittet, Y.Y. Shan, M. Herin

Research output: Contribution to journalArticlepeer-review

Abstract

Although Oxidosqualenes analogs bearing a E-Δ C,C double bond are cyclized by 2,3-oxidosqualene cyclase (EC 5.4.99.7, 'sterol cyclase') to produce 20-R norlanosterols, those possessing a Z-Δ C,C double bond instead produce, a mixture of 20-S norlanosterols and tricyclic derivatives whose ratio depends upon the length of the side chain.
Original languageEnglish
Pages (from-to)365-368
Number of pages4
JournalBioorganic & Medicinal Chemistry Letters
Volume3
Issue number2
DOIs
Publication statusPublished - 1 Jan 1993

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