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ChEBI
> Main
CHEBI:86075 - (24
S
,26)-dihydroxycholesterol
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ChEBI Ontology
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ChEBI Name
(24
S
,26)-dihydroxycholesterol
ChEBI ID
CHEBI:86075
ChEBI ASCII Name
(24S,26)-dihydroxycholesterol
Definition
An oxysterol that is cholesterol which is substituted by hydroxy groups at positions 24
S
and 26.
Stars
This entity has been manually annotated by the ChEBI Team.
Submitter
Nevila Nouspikel
Supplier Information
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Molfile
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Formula
C27H46O3
Net Charge
0
Average Mass
418.65230
Monoisotopic Mass
418.34470
InChI
InChI=1S/C27H46O3/c1-
17(5-
10-
25(30)
18(2)
16-
28)
22-
8-
9-
23-
21-
7-
6-
19-
15-
20(29)
11-
13-
26(19,3)
24(21)
12-
14-
27(22,23)
4/h6,17-
18,20-
25,28-
30H,5,7-
16H2,1-
4H3/t17-
,18?,20+,21+,22-
,23+,24+,25+,26+,27-
/m1/s1
InChIKey
XMULUVSUDUCTFU-WPFPFMOUSA-N
SMILES
CC(CO)[C@@H](O)CC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C
Roles Classification
Biological Role
(s):
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (
Homo sapiens
).
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
(24
S
,26)-dihydroxycholesterol (
CHEBI:86075
)
has functional parent
cholesterol (
CHEBI:16113
)
(24
S
,26)-dihydroxycholesterol (
CHEBI:86075
)
has role
human metabolite (
CHEBI:77746
)
(24
S
,26)-dihydroxycholesterol (
CHEBI:86075
)
is a
24-hydroxy steroid (
CHEBI:36865
)
(24
S
,26)-dihydroxycholesterol (
CHEBI:86075
)
is a
26-hydroxy steroid (
CHEBI:36852
)
(24
S
,26)-dihydroxycholesterol (
CHEBI:86075
)
is a
3β-hydroxy-Δ
5
-steroid (
CHEBI:1722
)
(24
S
,26)-dihydroxycholesterol (
CHEBI:86075
)
is a
3β-sterol (
CHEBI:35348
)
(24
S
,26)-dihydroxycholesterol (
CHEBI:86075
)
is a
oxysterol (
CHEBI:53030
)
IUPAC Name
(3β,24
S
)-cholest-5-ene-3,24,26-triol
Synonyms
Sources
24
S
,27-dihydroxycholesterol
UniProt
cholest-5-en-3β,24
S
,26-triol
LIPID MAPS
cholest-5-en-3β,24
S
,27-triol
SUBMITTER
Manual Xref
Database
LMST01010129
LIPID MAPS
View more database links
Registry Number
Type
Source
27356794
Reaxys Registry Number
Reaxys
Citation
Type
Source
14640697
PubMed citation
SUBMITTER
Last Modified
25 October 2017