Skip to Content
Merck
All Photos(1)

Documents

700118P

Avanti

zymostenol

powder

Synonym(s):

111112

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C27H46O
CAS Number:
Molecular Weight:
386.65
UNSPSC Code:
12352211
NACRES:
NA.25

form

powder

packaging

pkg of 1 × 1 mg (700118P-1mg)

manufacturer/tradename

Avanti Polar Lipids 700118P

shipped in

dry ice

storage temp.

−20°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

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 Code

11 - Combustible Solids


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 6

1 of 6

Avanti Polar Lipids

Avanti

700073P

14-demethyl-lanosterol

FF-MAS Avanti Polar Lipids

Avanti

700077P

FF-MAS

≥93%, powder

Sigma-Aldrich

L5768

Lanosterol

≥95.0% (HPLC)

Sigma-Aldrich

30800

7-Dehydrocholesterol

lanosterol Avanti Polar Lipids

Avanti

700063P

lanosterol

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)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service