CHEBI:34849 - mibolerone

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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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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.
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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-Δ4 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
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Registry Numbers Types Sources
3704-09-4 CAS Registry Number ChemIDplus
5565683 Reaxys Registry Number Reaxys
5565683 Beilstein Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
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Last Modified
04 June 2013