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Key Documents

700099P

Avanti

lanosterol-95

Avanti Research - A Croda Brand

Synonym(s):

lanosterin; lanosta-8,24-dienol

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About This Item

Empirical Formula (Hill Notation):
C30H50O
CAS Number:
Molecular Weight:
426.72
UNSPSC Code:
12352211
NACRES:
NA.25

description

8,24-lanostadien-3β-ol

Assay

>95% (TLC)

form

powder

packaging

pkg of 1 × 100 mg (700099P-100mg)
pkg of 1 × 5 mg (700099P-5mg)

manufacturer/tradename

Avanti Research - A Croda Brand

shipped in

dry ice

storage temp.

−20°C

InChI

1S/C30H50O/c1-20(2)10-9-11-21(3)22-14-18-30(8)24-12-13-25-27(4,5)26(31)16-17-28(25,6)23(24)15-19-29(22,30)7/h10,21-22,25-26,31H,9,11-19H2,1-8H3/t21-,22-,25+,26+,28-,29-,30+/m1/s1

InChI key

CAHGCLMLTWQZNJ-BQNIITSRSA-N

General description

Lanosterol is a lanostane-type tetracyclic triterpene. It is the first sterol in lipid biosynthetic pathway.

Biochem/physiol Actions

Lanosterol blocks cataract formation, inhibits lens opacity and reverses crystalline aggregation.

Packaging

5 mL Amber Glass Screw Cap Vial (700099P-100mg)
5 mL Amber Glass Screw Cap Vial (700099P-5mg)

Legal Information

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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’.

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Tetracyclic triterpenes from Inonotus obliquus (PERS.) PIL.(CHAGA) growing in Russia
Zhukovich EN, et al.
Pharmaceutical Chemistry Journal, 44(9), 495-496 (2010)
Lanosterol synthase pathway alleviates lens opacity in age-related cortical cataract
Shen X, et al.
Journal of Ophthalmology, 2018 (2018)

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