Structure Database (LMSD)

Common Name
5alpha-dihydrotesosterone
Systematic Name
17β-hydroxy-androstan-3-one
Synonyms
  • Stanolone
  • Androstanolone
LM ID
LMST02020042
Formula
C19H30O2
Exact Mass
Calculate m/z
290.22458
Sum Composition
ST 19:1;O2
Status
Curated
Show lipids differing only in stereochemistry/bond geometry
View MassBank spectra

Classification

Category
Main Class
Sub Class
Sterol Lipids [ST]
Steroids [ST02]
C19 steroids (androgens) and derivatives [ST0202]

Reactions

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ⓘ Reactions are shown if the E.C. number of the enzyme catalysing it is annotated in the UniProt database for a species belonging to the selected taxonomic class.
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Reactions graph legend

References

Taxonomy Information

Curated from
NCBI taxonomy class
Reference
Rattus norvegicus (#10116)
Mammalia (#40674)
In vitro conversion of testosterone to 17beta-hydroxyandrostan-3-one.,
Proc Soc Exp Biol Med, 1956
Pubmed ID: 13323010

String Representations

InChiKey (Click to copy)
NVKAWKQGWWIWPM-ABEVXSGRSA-N
InChi (Click to copy)
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/h12,14-17,21H,3-11H2,1-2H3/t12-,14-,15-,16-,17-,18-,19-/m0/s1
SMILES (Click to copy)
C1[C@]2(C)[C@@]3([H])CC[C@]4(C)[C@@H](O)CC[C@@]4([H])[C@]3([H])CC[C@@]2([H])CC(=O)C1

Other Databases

Wikipedia
Dihydrotestosterone
KEGG ID
C03917
HMDB ID
HMDB0002961
CHEBI ID
16330
LIPIDBANK ID
SST0297
PubChem CID
10635
SwissLipids ID
SLM:000001058
Cayman ID
15874
PDB ID
DHT
GuidePharm ID
3455

Calculated Physicochemical Properties

Heavy Atoms 21
Rings 4
Aromatic Rings 0
Rotatable Bonds 0
Van der Waals Molecular Volume 302.76
Topological Polar Surface Area 37.30
Hydrogen Bond Donors 1
Hydrogen Bond Acceptors 2
logP 4.25
Molar Refractivity 83.25

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Created at
-
Updated at
16th Jan 2024