Ergosterol

CAS : 57-87-4

Ref. 3D-FE30866

Informations sur le produit

• Nom: Ergosterol
• Synonymes: 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, 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 D₂
• CAS: 57-87-4

Description

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.

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 396.65 g/mol
• Formule: C₂₈H₄₄O
• Degré de pureté: Min. 97 Area-%
• Couleur/Forme: White Powder