B4936
Brassicasterol
from semisynthetic
Synonym(s):
5,22-Cholestadien-24β-methyl-3β-ol
About This Item
Recommended Products
biological source
semisynthetic
Assay
≥98% (TLC)
form
powder
shipped in
wet ice
storage temp.
2-8°C
SMILES string
CC(C)[C@@H](C)\C=C\[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C
InChI
1S/C28H46O/c1-18(2)19(3)7-8-20(4)24-11-12-25-23-10-9-21-17-22(29)13-15-27(21,5)26(23)14-16-28(24,25)6/h7-9,18-20,22-26,29H,10-17H2,1-6H3/b8-7+/t19-,20+,22-,23-,24+,25-,26-,27-,28+/m0/s1
InChI key
OILXMJHPFNGGTO-ZAUYPBDWSA-N
Related Categories
Application
Biochem/physiol Actions
Preparation Note
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Certificates of Analysis (COA)
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Articles
The amount of cholesterol that is synthesized in the liver is tightly regulated by dietary cholesterol levels. LDL receptors regulate the cellular transport of lipid rich low density lipoprotein (LDL) particles.
Protocols
Separation of Cholesterol; Brassicasterol; Campesterol; Stigmasterol; β-Sitosterol
Separation of Cholesterol; Brassicasterol; Campesterol; Stigmasterol; β-Sitosterol
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