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InChI=1S/CH4O/c1-2/h2H,1H3
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> Main
CHEBI:132823 - clionasterol
Main
ChEBI Ontology
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ChEBI Name
clionasterol
ChEBI ID
CHEBI:132823
Definition
A member of the class of phytosterols that is poriferast-5-ene carrying a β-hydroxy substituent at position 3.
Stars
This entity has been manually annotated by the ChEBI Team.
Submitter
qingping liu
Supplier Information
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Molfile
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Formula
C29H50O
Net Charge
0
Average Mass
414.708
Monoisotopic Mass
414.38617
InChI
InChI=1S/C29H50O/c1-
7-
21(19(2)
3)
9-
8-
20(4)
25-
12-
13-
26-
24-
11-
10-
22-
18-
23(30)
14-
16-
28(22,5)
27(24)
15-
17-
29(25,26)
6/h10,19-
21,23-
27,30H,7-
9,11-
18H2,1-
6H3/t20-
,21+,23+,24+,25-
,26+,27+,28+,29-
/m1/s1
InChIKey
KZJWDPNRJALLNS-FBZNIEFRSA-N
SMILES
C1[C@@]
2([C@]
3(CC[C@]
4([C@]
([C@@]
3(CC=C2C[C@H]
(C1)
O)
[H]
)
(CC[C@@]
4([C@H]
(C)
CC[C@@H]
(C(C)
C)
CC)
[H]
)
[H]
)
C)
[H]
)
C
Metabolite of Species
Details
Dragmacidon coccineum
(NCBI:txid1807045)
See:
PubMed
Polygala tenuifolia
(NCBI:txid355332)
Found in rhizome
(BTO:0001181)
. See:
PubMed
Elaeis guineensis
(NCBI:txid51953)
See:
PubMed
Roles Classification
Biological Role
(s):
plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
marine metabolite
Any metabolite produced during a metabolic reaction in marine macro- and microorganisms.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
clionasterol (
CHEBI:132823
)
has parent hydride
poriferastane (
CHEBI:26211
)
clionasterol (
CHEBI:132823
)
has role
marine metabolite (
CHEBI:76507
)
clionasterol (
CHEBI:132823
)
has role
plant metabolite (
CHEBI:76924
)
clionasterol (
CHEBI:132823
)
is a
3β-hydroxy-Δ
5
-steroid (
CHEBI:1722
)
clionasterol (
CHEBI:132823
)
is a
3β-sterol (
CHEBI:35348
)
clionasterol (
CHEBI:132823
)
is a
phytosterols (
CHEBI:26125
)
IUPAC Name
(24
S
)-stigmast-5-en-3β-ol
Synonyms
Sources
(3β,24
S
)-stigmast-5-en-3-ol
IUPAC
22,23-Dihydroporiferasterol
NIST Chemistry WebBook
24-Ethylcholest-5-en-3 beta-ol
HMDB
24β-ethyl-5-cholesten-3β-ol
NIST Chemistry WebBook
24β-ethylcholesterol
HMDB
24
S
-ethylcholest-5-en-3β-ol
HMDB
β-dihydrofucosterol
NIST Chemistry WebBook
γ-sitosterol
HMDB
gamma-Sitosterol
KNApSAcK
poriferast-5-en-3β-ol
LIPID MAPS
Manual Xrefs
Databases
C00023769
KNApSAcK
HMDB0000649
HMDB
LMST01040122
LIPID MAPS
View more database links
Registry Numbers
Types
Sources
2061922
Reaxys Registry Number
Reaxys
83-47-6
CAS Registry Number
NIST Chemistry WebBook
83-47-6
CAS Registry Number
ChemIDplus
Citations
Types
Sources
22863942
PubMed citation
Europe PMC
24417147
PubMed citation
Europe PMC
24831420
PubMed citation
Europe PMC
26710827
PubMed citation
Europe PMC
27694009
PubMed citation
Europe PMC
Last Modified
25 April 2017