Produktinformation
- Provitamin D2 3beta-Hydroxy-5,7,22-ergostatriene
- (22E)-Ergosta-5,7,22-trien-3beta-ol
- (22E)-ergosta-5,7,22-trien-3-ol
- (22E,24R)-Ergosta-5,7,22-trien-3β-ol
- (24R)-Ergosta-5,7,22-trien-3β-ol
- (3S,9S,10R,13R,17R)-10,13-dimethyl-17-[(E)-1,4,5-trimethylhex-2-enyl]-2,3,4,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol
- (3beta,22E)-ergosta-5,7,22-trien-3-ol
- (3β,22E)-Ergosta-5,7,22-trien-3-ol
- 24-Methylcholesta-5,7,22-trien-3β-ol
- 24R-Methylcholesta-5,7,22E-trien-3β-ol
- Mehr Synonyme anzeigen
- 24α-Methyl-22E-dehydrocholesterol
- 3β-Hydroxyergosta-5,7,22-triene
- Ergosta-5,7,22-Trien-3-Ol
- Ergosta-5,7,22-trien-3-ol, (3β,22E)-
- Ergosterin
- Provitamin D
- Provitamin D2
- Provitamin D<sub>2</sub>
Ergosterol is a sterol that is found in fungi. It acts as a cofactor for enzymes such as the cytochrome P450 system and the fungal-specific enzyme, lanosterol 14α-demethylase. Ergosterol has been shown to inhibit melanogenesis in wild-type strains of yeast and human cells. Ergosterol also binds to DNA, which may be responsible for its cytosolic Ca2+ regulation and nuclear DNA binding activity. This sterol also plays a role in iron homeostasis through its effects on heme synthesis, which is important for cellular respiration. Ergosterol has also been shown to have anti-inflammatory pharmacological activities against Candida glabrata.
Chemische Eigenschaften
Technische Anfrage zu: 3D-FE30866 Ergosterol
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