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About This Item
Empirical Formula (Hill Notation):
C30H50O
CAS Number:
Molecular Weight:
426.72
MDL number:
UNSPSC Code:
12352211
NACRES:
NA.25
description
8,24-lanostadien-3β-ol
assay
>99% (TLC)
form
powder
packaging
pkg of 1 × 1 mg (700063P-1mg), pkg of 1 × 10 mg (700063P-10mg), pkg of 1 × 5 mg (700063P-5mg)
manufacturer/tradename
Avanti Research™ - A Croda Brand
shipped in
dry ice
storage temp.
−20°C
SMILES string
O[C@@H]1C([C@H]2[C@](CC1)(C3=C([C@]4([C@@]([C@H](CC4)[C@@H](CCC=C(C)C)C)(CC3)C)C)CC2)C)(C)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, which is the first sterol in lipid biosynthetic pathway.
Biochem/physiol Actions
Lanosterol inhibits cataract formation, prevents lens opacity and reverses crystalline aggregation.
Packaging
5 mL Amber Glass Screw Cap Vial (700063P-10mg)
5 mL Amber Glass Screw Cap Vial (700063P-1mg)
5 mL Amber Glass Screw Cap Vial (700063P-5mg)
Legal Information
Avanti Research is a trademark of Avanti Polar Lipids, LLC
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Storage Class
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
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Tetracyclic triterpenes from Inonotus obliquus (PERS.) PIL.(CHAGA) growing in Russia
Zhukovich EN, et al.
Pharmaceutical Chemistry Journal, 2018, 495-496 (2010)
Lanosterol synthase pathway alleviates lens opacity in age-related cortical cataract
Shen X, et al.
Journal of Ophthalmology, 41(4), 744-747 (2018)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 700063P-10MG | 04061835384723 |
| 700063P-1MG | 04061835384730 |
| 700063P-5MG | 04061835384747 |