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lanosterol (CHEBI:16521)

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ChEBI Name lanosterol
ChEBI ID CHEBI:16521
Definition A tetracyclic triterpenoid that is lanosta-8,24-diene substituted by a β-hydroxy group at position 3. It is the compound from which all steroids are derived.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:43584, CHEBI:6374, CHEBI:14500, CHEBI:25011
Supplier Information
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Formula Source
C30H50O KEGG COMPOUND
Net Charge 0
Average Mass 426.71740
InChI
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
InChIKey
CAHGCLMLTWQZNJ-BQNIITSRSA-N
SMILES
[H][C@@]1(CC[C@@]2(C)C3=C(CC[C@]12C)[C@@]1(C)CC[C@H](O)C(C)(C)[C@]1([H])CC3)[C@H](C)CCC=C(C)C
Metabolite of Species Source
Isolated from Homo sapiens (NCBI:9606) DOI
Roles Classification
Biological Role(s): human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
bacterial metabolite
Any prokaryotic metabolite produced during a metabolic reaction in bacteria.
plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
View more on the ChEBI Ontology
ChEBI Ontology
Outgoing lanosterol (CHEBI:16521) has parent hydride lanostane (CHEBI:20265)
lanosterol (CHEBI:16521) has role bacterial metabolite (CHEBI:76969)
lanosterol (CHEBI:16521) has role human metabolite (CHEBI:77746)
lanosterol (CHEBI:16521) has role plant metabolite (CHEBI:76924)
lanosterol (CHEBI:16521) is a 3β-sterol (CHEBI:35348)
lanosterol (CHEBI:16521) is a tetracyclic triterpenoid (CHEBI:26893)
Incoming 14-demethyllanosterol (CHEBI:18364) has functional parent lanosterol (CHEBI:16521)
24,25-dihydrolanosterol (CHEBI:28113) has functional parent lanosterol (CHEBI:16521)
lanosteryl ester (CHEBI:52394) has functional parent lanosterol (CHEBI:16521)
IUPAC Name
lanosta-8,24-dien-3β-ol
Synonyms Sources
(3β)-lanosta-8,24-dien-3-ol ChemIDplus
(3β,5α)-4,4,14-trimethylcholesta-8,24-dien-3-ol ChemIDplus
4,4',14alpha-Trimethyl-5alpha-cholesta-8,24-dien-3beta-ol KEGG COMPOUND
Lanosterin HMDB
Lanosterol KEGG COMPOUND
LANOSTEROL PDBeChem
lanosterol UniProt
Database Links Databases
C00003657 KNApSAcK
C01724 KEGG COMPOUND
DB03696 DrugBank
HMDB01251 HMDB
LAN PDBeChem
Lanosterol Wikipedia
LANOSTEROL MetaCyc
LMST01010017 LIPID MAPS
View more database links
Registry Numbers Types Sources
2226449 Beilstein Registry Number ChemIDplus
2226449 Reaxys Registry Number Reaxys
79-63-0 CAS Registry Number KEGG COMPOUND
79-63-0 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
14660793 PubMed citation CiteXplore
22988818 PubMed citation CiteXplore
24525128 PubMed citation CiteXplore
Last Modified
28 July 2014

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