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> Main
CHEBI:17168 - 5α-cholest-7-en-3β-ol
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ChEBI Name
5α-cholest-7-en-3β-ol
ChEBI ID
CHEBI:17168
ChEBI ASCII Name
5alpha-cholest-7-en-3beta-ol
Definition
A cholestanoid that is (5α)-cholest-7-ene substituted by a β-hydroxy group at position 3.
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:12169, CHEBI:2138, CHEBI:20643
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Formula
C27H46O
Net Charge
0
Average Mass
386.65354
Monoisotopic Mass
386.35487
InChI
InChI=1S/C27H46O/c1-
18(2)
7-
6-
8-
19(3)
23-
11-
12-
24-
22-
10-
9-
20-
17-
21(28)
13-
15-
26(20,4)
25(22)
14-
16-
27(23,24)
5/h10,18-
21,23-
25,28H,6-
9,11-
17H2,1-
5H3/t19-
,20+,21+,23-
,24+,25+,26+,27-
/m1/s1
InChIKey
IZVFFXVYBHFIHY-SKCNUYALSA-N
SMILES
[H][C@@]12CC=C3[C@]4([H])CC[C@]([H])([C@H](C)CCCC(C)C)[C@@]4(C)CC[C@]3([H])[C@@]1(C)CC[C@H](O)C2
Metabolite of Species
Details
Mus musculus
(NCBI:txid10090)
See:
PubMed
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
5α-cholest-7-en-3β-ol (
CHEBI:17168
)
has role
human metabolite (
CHEBI:77746
)
5α-cholest-7-en-3β-ol (
CHEBI:17168
)
has role
mouse metabolite (
CHEBI:75771
)
5α-cholest-7-en-3β-ol (
CHEBI:17168
)
is a
Δ
7
-sterol (
CHEBI:138130
)
5α-cholest-7-en-3β-ol (
CHEBI:17168
)
is a
3β-sterol (
CHEBI:35348
)
5α-cholest-7-en-3β-ol (
CHEBI:17168
)
is a
C
27
-steroid (
CHEBI:131619
)
5α-cholest-7-en-3β-ol (
CHEBI:17168
)
is a
cholestanoid (
CHEBI:50401
)
Incoming
cholestanol 7α,8α-epoxide (
CHEBI:137063
)
has functional parent
5α-cholest-7-en-3β-ol (
CHEBI:17168
)
Synonyms
Sources
5alpha-cholest-7-en-3beta-ol
ChEBI
5alpha-Cholest-7-en-3beta-ol
KEGG COMPOUND
5α-cholest-7-en-3β-ol
ChEBI
5alpha-Cholest-7-en-3beta-ol
KEGG COMPOUND
gamma-Cholesterol
ChemIDplus
Lathosterol
KEGG COMPOUND
lathosterol
UniProt
Manual Xrefs
Databases
C00023744
KNApSAcK
C01189
KEGG COMPOUND
HMDB0001170
HMDB
Lathosterol
Wikipedia
LMST01010089
LIPID MAPS
View more database links
Registry Numbers
Types
Sources
3215566
Reaxys Registry Number
Reaxys
80-99-9
CAS Registry Number
KEGG COMPOUND
80-99-9
CAS Registry Number
ChemIDplus
Citations
Types
Sources
12812989
PubMed citation
Europe PMC
14511438
PubMed citation
Europe PMC
Last Modified
09 May 2022