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About This Item
Empirical Formula (Hill Notation):
C27H46O
CAS Number:
Molecular Weight:
386.65
MDL number:
UNSPSC Code:
12352211
NACRES:
NA.25
Product Name
zymostenol, Avanti Research™ - A Croda Brand
packaging
pkg of 1 × 1 mg (700118P-1mg)
manufacturer/tradename
Avanti Research™ - A Croda Brand
SMILES string
O[C@@H]1C[C@H]2[C@](CC1)(C3=C([C@H]4[C@@]([C@H](CC4)[C@@H](CCCC(C)C)C)(CC3)C)CC2)C
InChI
1S/C27H46O/c1-18(2)7-6-8-19(3)23-11-12-24-22-10-9-20-17-21(28)13-15-26(20,4)25(22)14-16-27(23,24)5/h18-21,23-24,28H,6-17H2,1-5H3/t19-,20+,21+,23-,24+,26+,27-/m1/s1
InChI key
QETLKNDKQOXZRP-XTGBIJOFSA-N
assay
>99% (TLC)
form
powder
shipped in
dry ice
storage temp.
−20°C
General description
Zymostenol acts as a substrate for Δ8,7-sterol isomerase (EBP). It is a demethylation product of 24,25-dihydrolanosterol (24,25-DHL).
Application
Zymostenol has been used to study its accumulation and its inhibitory actions on Δ8,7-sterol isomerase (EBP).
Packaging
5 mL Amber Glass Screw Cap Vial (700118P-1mg)
Legal Information
Avanti Research is a trademark of Avanti Polar Lipids, LLC
Storage Class
11 - Combustible Solids
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Diverse Chemical Scaffolds Enhance Oligodendrocyte Formation by Inhibiting CYP51, TM7SF2, or EBP
Allimuthu D, et al.
Cell Chemical Biology (2019)
Insig-mediated degradation of HMG CoA reductase stimulated by lanosterol, an intermediate in the synthesis of cholesterol
Song BL, et al.
Cell Metabolism, 1(3), 179-189 (2005)
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