Lumisterol Explained

Lumisterol is a compound that is part of the vitamin D family of steroid compounds. It is the (9β,10α) stereoisomer of ergosterol and was produced as a photochemical by-product in the preparation of vitamin D1, which was a mixture of vitamin D2 and lumisterol.[1] [2] Vitamin D2 can be formed from lumisterol by an electrocyclic ring opening and subsequent sigmatropic [1,7] hydride shift. Lumisterol has an analog based on 7-dehydrocholesterol, known as lumisterol 3.[3]

References

  1. Book: Dewick, Paul M.. Medicinal Natural Products. A Biosynthetic Approach. Second. 2002. John Wiley & Sons. New York. 0-471-49640-5. 259.
  2. Book: Friedmann, Ernst. Neurath, Hans. Vitamin D. Perspectives in Biochemistry. 1. 1989. American Chemical Society. Washington, DC. 978-0-8412-1621-1.
  3. Web site: National Center for Biotechnology Information. Lumisterol 3 (CID=111049). PubChem Compound Database. 10 April 2018. en.