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Chemical compound
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
Lumisterol
Intramolecular organic reaction in which a sigma bond is changed
final electrocyclic ring-closing reaction, in the interconversion of lumisterol to vitamin D2. [1,7] sigmatropic shifts are predicted by the Woodward–Hoffmann
Sigmatropic_reaction
Nutrients required by organisms in small amounts
vegetables, liver D D1 mixture of molecular compounds of ergocalciferol with lumisterol, 1:1 fat 15 μg/15 μg vitamin D deficiency hypervitaminosis D D2 ergocalciferol
Vitamin
Essential nutrient
Structure Vitamin D1 Mixture of molecular compounds of ergocalciferol with lumisterol, 1:1 Vitamin D2 ergocalciferol (made from ergosterol) Vitamin D3 cholecalciferol
Vitamin_D
Chemical compound
of ergosterol. Forms of vitamin D, the five known forms of vitamin D Lumisterol, a constituent of vitamin D1 Nomenclature of Vitamin D Archived 2017-08-23
22-Dihydroergocalciferol
Edible fungi fruit bodies
Name Chemical composition Structure Vitamin D1 ergocalciferol with lumisterol, 1:1 Vitamin D2 ergocalciferol (made from ergosterol) Vitamin D3 cholecalciferol
Edible_mushroom
Index of chemical compounds with the same molecular formula
may refer to: 5-Dehydroepisterol Ergocalciferol Ergosterol Lichesterol Lumisterol This set index page lists chemical structure articles associated with
C28H44O
Mammalian protein found in humans
reductase (DHCR7) to act on some 7-Dehydrocholesterol metabolites but not on lumisterol metabolites". The Journal of Steroid Biochemistry and Molecular Biology
7-Dehydrocholesterol reductase
7-Dehydrocholesterol_reductase
Group of chemical reactions
"366. Steroids of unnatural configuration. Part IX. Oxidation of 9α-lumisterol (pyrocalciferol) and 9β-ergosterol (isopyrocalciferol) with perbenzoic
Epoxidation of allylic alcohols
Epoxidation_of_allylic_alcohols
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