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ChEBI
> Main
CHEBI:34849 - mibolerone
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ChEBI Ontology
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ChEBI Name
mibolerone
ChEBI ID
CHEBI:34849
Definition
An androgen that is nalandrone carrying two methyl substituents at positions 7α and 17.
Stars
This entity has been manually annotated by the ChEBI Team.
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Wikipedia
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Read full article at Wikipedia
Formula
C20H30O2
Net Charge
0
Average Mass
302.45100
Monoisotopic Mass
302.22458
InChI
InChI=1S/C20H30O2/c1-
12-
10-
13-
11-
14(21)
4-
5-
15(13)
16-
6-
8-
19(2)
17(18(12)
16)
7-
9-
20(19,3)
22/h11-
12,15-
18,22H,4-
10H2,1-
3H3/t12-
,15+,16-
,17+,18-
,19+,20+/m1/s1
InChIKey
PTQMMNYJKCSPET-OMHQDGTGSA-N
SMILES
[H][C@]12CCC(=O)C=C1C[C@@H](C)[C@]1([H])[C@]2([H])CC[C@@]2(C)[C@@]1([H])CC[C@]2(C)O
Roles Classification
Biological Role
(s):
anabolic agent
A compound which stimulates anabolism and inhibits catabolism. Anabolic agents stimulate the development of muscle mass, strength, and power.
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
mibolerone (
CHEBI:34849
)
has parent hydride
estrane (
CHEBI:23966
)
mibolerone (
CHEBI:34849
)
has role
anabolic agent (
CHEBI:36413
)
mibolerone (
CHEBI:34849
)
has role
androgen (
CHEBI:50113
)
mibolerone (
CHEBI:34849
)
is a
17β-hydroxy steroid (
CHEBI:35343
)
mibolerone (
CHEBI:34849
)
is a
3-oxo-Δ
4
steroid (
CHEBI:47909
)
IUPAC Name
17β-hydroxy-7α,17-dimethylestr-4-en-3-one
INNs
Sources
mibolerona
ChemIDplus
mibolerone
KEGG DRUG
mibolérone
WHO MedNet
miboleronum
ChemIDplus
Synonyms
Sources
(7α,17β)-17-hydroxy-7,17-dimethylestr-4-en-3-one
IUPAC
17-beta-Hydroxy-7-alpha,17-dimethylestr-4-en-3-one
KEGG COMPOUND
7α-17α-dimethyl-19-nortestosterone
ChemIDplus
NSC 72260
ChemIDplus
U 10997
ChemIDplus
U-10,997
ChemIDplus
Manual Xrefs
Databases
C14255
KEGG COMPOUND
D05025
KEGG DRUG
Mibolerone
Wikipedia
US2002012694
Patent
US2002193359
Patent
US4412993
Patent
US5342834
Patent
View more database links
Registry Numbers
Types
Sources
3704-09-4
CAS Registry Number
ChemIDplus
5565683
Reaxys Registry Number
Reaxys
5565683
Beilstein Registry Number
ChemIDplus
Citations
Types
Sources
18515094
PubMed citation
Europe PMC
18770362
PubMed citation
Europe PMC
209430
PubMed citation
Europe PMC
2151880
PubMed citation
Europe PMC
2410244
PubMed citation
Europe PMC
2417401
PubMed citation
Europe PMC
2422638
PubMed citation
Europe PMC
3265669
PubMed citation
Europe PMC
3930306
PubMed citation
Europe PMC
3934110
PubMed citation
Europe PMC
405963
PubMed citation
Europe PMC
4070927
PubMed citation
Europe PMC
565606
PubMed citation
Europe PMC
6254486
PubMed citation
Europe PMC
869826
PubMed citation
Europe PMC
921032
PubMed citation
Europe PMC
Last Modified
04 June 2013