lanosterolo

Also known as (3β)-lanosta-8,24-dien-3-ol, (3β,20R)-lanosta-8,24-dien-3-ol, lanosterin, (3beta,5alpha)-4,4,14-trimethylcholesta-8,24-dien-3-ol, (3beta)-lanosta-8,24-dien-3-ol, (2S,5S,7R,11R,14R,15R)-2,6,6,11,15-pentamethyl-14-[(2R)-6-methylhept-5-en-2-yl]tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-1(10)-en-5-ol, (3 beta)-lanosta-8,24-dien-3-ol, (3beta,5alpha)-4,4,14-trimethyl-cholesta-8,24-dien-3-ol

farmaco

In the Vinony graph

Vinony's link graph records 337 inbound references to lanosterolo, and connects out to triterpene, squalene oxide and digital object identifier.

It sits within the topics Chembox image size set, ECHA InfoCard ID from Wikidata and Lanostanes.

Vinony links it to 25 Wikipedia language editions.

Chemical data

Formula: C30H50O
Molecular weight: 426.7 g/mol
IUPAC name: (3S,5R,10S,13R,14R,17R)-4,4,10,13,14-pentamethyl-17-[(2R)-6-methylhept-5-en-2-yl]-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol
SMILES: C[C@H](CCC=C(C)C)[C@H]1CC[C@@]2([C@@]1(CCC3=C2CC[C@@H]4[C@@]3(CC[C@@H](C4(C)C)O)C)C)C
InChIKey: CAHGCLMLTWQZNJ-BQNIITSRSA-N
XLogP: 8.9
Polar surface area: 20.2 Å²
H-bond donors: 1
H-bond acceptors: 1
Formal charge: 0

via PubChem

Drug data · ChEMBL

Molecule type: Small molecule

via ChEMBL · EBI

Research

2,896 papers

Lanosterol reverses protein aggregation in cataracts.Nature · 2015
Ergosterol and Lanosterol Derivatives: Synthesis and Possible Biomedical Applications.ChemMedChem · 2025
Post-lanosterol biosynthesis of cholesterol and cancer.Current opinion in pharmacology · 2012
Lanosterol analogs: dual-action inhibitors of cholesterol biosynthesis.Critical reviews in biochemistry and molecular biology · 1999
Lanosterol Disrupts the Aggregation of Amyloid-β Peptides.ACS chemical neuroscience · 2019

via PubMed

Wikidata facts

Has part: carbon
Mass: 426.386

Show 6 more facts

found in taxon: Lingulodinium polyedra
chemical formula: C₃₀H₅₀O
Commons category: Lanosterol
canonical SMILES: CC(CCC=C(C)C)C1CCC2(C1(CCC3=C2CCC4C3(CCC(C4(C)C)O)C)C)C
isomeric SMILES: C[C@H](CCC=C(C)C)[C@H]1CC[C@@]2([C@@]1(CCC3=C2CC[C@@H]4[C@@]3(CC[C@@H](C4(C)C)O)C)C)C
subject has role: primary metabolite

Sources (5)

via Wikidata · CC0