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
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
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
存储类别
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
Lanosterol synthase pathway alleviates lens opacity in age-related cortical cataract
Shen X, et al.
Journal of Ophthalmology, 2018 (2018)
Tetracyclic triterpenes from Inonotus obliquus (PERS.) PIL.(CHAGA) growing in Russia
Zhukovich EN, et al.
Pharmaceutical Chemistry Journal, 44(9), 495-496 (2010)
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