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CHEBI:541975 - epiandrosterone
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ChEBI Ontology
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ChEBI Name
epiandrosterone
ChEBI ID
CHEBI:541975
Definition
A 3β-hydroxy steroid that is (5α)-androstane substituted by a β-hydroxy group at position 3 and an oxo group at position 17.
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:4802
Supplier Information
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Read full article at Wikipedia
Formula
C19H30O2
Net Charge
0
Average Mass
290.44030
Monoisotopic Mass
290.22458
InChI
InChI=1S/C19H30O2/c1-
18-
9-
7-
13(20)
11-
12(18)
3-
4-
14-
15-
5-
6-
17(21)
19(15,2)
10-
8-
16(14)
18/h12-
16,20H,3-
11H2,1-
2H3/t12-
,13-
,14-
,15-
,16-
,18-
,19-
/m0/s1
InChIKey
QGXBDMJGAMFCBF-LUJOEAJASA-N
SMILES
[H][C@@]12CC[C@@]3([H])[C@]4([H])CCC(=O)[C@@]4(C)CC[C@]3([H])[C@@]1(C)CC[C@H](O)C2
Roles Classification
Biological Role
(s):
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (
Homo sapiens
).
androgen
A sex hormone that stimulates or controls the development and maintenance of masculine characteristics in vertebrates by binding to androgen receptors.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
epiandrosterone (
CHEBI:541975
)
has functional parent
5α-androstane (
CHEBI:28859
)
epiandrosterone (
CHEBI:541975
)
has role
androgen (
CHEBI:50113
)
epiandrosterone (
CHEBI:541975
)
has role
human metabolite (
CHEBI:77746
)
epiandrosterone (
CHEBI:541975
)
is a
17-oxo steroid (
CHEBI:19168
)
epiandrosterone (
CHEBI:541975
)
is a
3β-hydroxy steroid (
CHEBI:36836
)
epiandrosterone (
CHEBI:541975
)
is a
androstanoid (
CHEBI:50402
)
Incoming
3β-hydroxy-5α-androstane-7,17-dione (
CHEBI:79834
)
has functional parent
epiandrosterone (
CHEBI:541975
)
7β-hydroxyepiandrosterone (
CHEBI:183809
)
has functional parent
epiandrosterone (
CHEBI:541975
)
epiandrosterone 3-β-
D
-glucoside (
CHEBI:145048
)
has functional parent
epiandrosterone (
CHEBI:541975
)
epiandrosterone sulfate (
CHEBI:83040
)
has functional parent
epiandrosterone (
CHEBI:541975
)
IUPAC Name
3β-hydroxy-5α-androstan-17-one
Synonyms
Sources
3-Epiandrosterone
ChemIDplus
3β-hydroxy-5α-androstan-17-one
UniProt
3β-Hydroxyetioallocholan-17-one
ChemIDplus
d-Epiandrosterone
ChemIDplus
iso-Androsterone
ChemIDplus
Isoandrosterone
ChemIDplus
Manual Xrefs
Databases
C07635
KEGG COMPOUND
CPD-13750
MetaCyc
Epiandrosterone
Wikipedia
HMDB0000365
HMDB
LMST02020023
LIPID MAPS
View more database links
Registry Numbers
Types
Sources
1884007
Reaxys Registry Number
Reaxys
481-29-8
CAS Registry Number
KEGG COMPOUND
481-29-8
CAS Registry Number
ChemIDplus
Citations
Types
Sources
12039447
PubMed citation
Europe PMC
12054855
PubMed citation
Europe PMC
12475725
PubMed citation
Europe PMC
15650074
PubMed citation
Europe PMC
15784286
PubMed citation
Europe PMC
15954157
PubMed citation
Europe PMC
16040239
PubMed citation
Europe PMC
17017935
PubMed citation
Europe PMC
17716701
PubMed citation
Europe PMC
18307294
PubMed citation
ChEMBL
6330917
PubMed citation
Europe PMC
8476769
PubMed citation
Europe PMC
Last Modified
18 November 2021