41719

(3S)-2,3-Oxidosqualene

≥97.5% (HPLC)

• Synonyme(s) : (S)-2,3-Epoxy-2,3-dihydrosqualene, (S)-22,23-Epoxy-2,6,10,15,19,23-hexamethyl-2,6,10,14,18-tetracosapentaene, (S)-Squalene 2,3-epoxide, (S)-Squalene 2,3-oxide
• Formule empirique (notation de Hill): C₃₀H₅₀O
• Numéro CAS: 54910-48-4
• Poids moléculaire : 426.72
• Numéro MDL: MFCD28100799
• Code UNSPSC : 12352204
• ID de substance PubChem : 329756144
• Nomenclature NACRES : NA.28

Propriétés

• Pureté: ≥97.5% (HPLC)
• Forme: liquid
• Pureté optique: enantiomeric excess: ≥90.0%
• Adéquation: conforms to structure for Proton NMR spectrum
• Température de stockage: −20°C
• Chaîne SMILES: CC1(C)O[C@H]1CC/C(C)=C/CC/C(C)=C/CC/C=C(C)/CC/C=C(C)/CCC=C(C)C
• InChI: 1S/C30H50O/c1-24(2)14-11-17-27(5)20-12-18-25(3)15-9-10-16-26(4)19-13-21-28(6)22-23-29-30(7,8)31-29/h14-16,20-21,29H,9-13,17-19,22-23H2,1-8H3/b25-15+,26-16+,27-20+,28-21+/t29-/m0/s1
• Clé InChI: QYIMSPSDBYKPPY-RSKUXYSASA-N

Description

Application

• Schizophrenic behavior of 2,3-Oxidosqualene Sterol Cyclase from pig liver towards 2,3-oxidosqualene analogues. Alain Krief and colleagues discuss the variable catalytic behaviors of oxidosqualene cyclase when interacting with different oxidosqualene analogues, suggesting implications for sterol production efficiency and specificity (Krief et al., 2021).

Actions biochimiques/physiologiques

(S)-2,3-Epoxysqualene is an intermediate of many metabolic pathways such as the steroid biosynthesis, sesquiterpenoid and triterpenoid biosynthesis, biosynthesis of plant secondary metabolites, biosynthesis of terpenoids and steroids, biosynthesis of plant hormones, biosynthesis of secondary metabolites, and biosynthesis of antibiotics.

Informations sur la sécurité

• Code de la classe de stockage: 10 - Combustible liquids
• Classe de danger pour l'eau (WGK): WGK 3
• Point d'éclair (°F): Not applicable
• Point d'éclair (°C): Not applicable