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> Main
CHEBI:28113 - 24,25-dihydrolanosterol
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ChEBI Name
24,25-dihydrolanosterol
ChEBI ID
CHEBI:28113
Definition
A 3β-sterol formed from lanosterol by reduction across the C-24‒C-25 double bond.
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:1303, CHEBI:19807
Supplier Information
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Formula
C30H52O
Net Charge
0
Average Mass
428.73328
Monoisotopic Mass
428.40182
InChI
InChI=1S/C30H52O/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/h20-
22,25-
26,31H,9-
19H2,1-
8H3/t21-
,22-
,25+,26+,28-
,29-
,30+/m1/s1
InChIKey
MBZYKEVPFYHDOH-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)CCCC(C)C
Metabolite of Species
Details
Mus musculus
(NCBI:txid10090)
Source: BioModels - MODEL1507180067 See:
PubMed
Homo sapiens
(NCBI:txid9606)
See:
DOI
Roles Classification
Biological Role
(s):
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (
Homo sapiens
).
mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (
Mus musculus
).
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
24,25-dihydrolanosterol (
CHEBI:28113
)
has functional parent
lanosterol (
CHEBI:16521
)
24,25-dihydrolanosterol (
CHEBI:28113
)
has role
human metabolite (
CHEBI:77746
)
24,25-dihydrolanosterol (
CHEBI:28113
)
has role
mouse metabolite (
CHEBI:75771
)
24,25-dihydrolanosterol (
CHEBI:28113
)
is a
3β-sterol (
CHEBI:35348
)
24,25-dihydrolanosterol (
CHEBI:28113
)
is a
tetracyclic triterpenoid (
CHEBI:26893
)
Incoming
eburicol (
CHEBI:70315
)
has functional parent
24,25-dihydrolanosterol (
CHEBI:28113
)
IUPAC Name
lanost-8-en-3β-ol
Synonyms
Sources
24,25-Dihydrolanosterol
KEGG COMPOUND
24,25-dihydrolanosterol
UniProt
Lanostenol
ChemIDplus
Manual Xrefs
Databases
C00023781
KNApSAcK
C05109
KEGG COMPOUND
CPD-8606
MetaCyc
HMDB0006839
HMDB
LMST01010087
LIPID MAPS
View more database links
Registry Numbers
Types
Sources
2224904
Beilstein Registry Number
Beilstein
2224904
Reaxys Registry Number
Reaxys
79-62-9
CAS Registry Number
KEGG COMPOUND
79-62-9
CAS Registry Number
ChemIDplus
Citation
Type
Source
898228
PubMed citation
Europe PMC
Last Modified
03 October 2017