Structure Database (LMSD)
Common Name
Androsterone
Systematic Name
3α-hydroxy-5α-androstan-17-one
Synonyms
- Androsterone
LM ID
LMST02020001
Formula
Exact Mass
Calculate m/z
290.22458
Sum Composition
Status
Curated
3D model of Androsterone
Please note: Where there are chiral atoms but the stereochemistry is undefined, the 3D model takes an arbitrary conformation
Classification
Category
Main Class
Sub Class
Biological Context
Androsterone is a steroid hormone produced in the body from 5α-reduced metabolites of dehydroepiandrosterone and possesses 7-fold weaker androgen potency compared to that of testosterone (Item No. 15645).1 It is the major androgen excreted in urine as a metabolite of testosterone and is used as the international reference standard for androgenic activity.1
This information has been provided by Cayman Chemical
References
1. de Gruyter, W. Androsterone. Concise encyclopedia biology 49 (1996).
String Representations
InChiKey (Click to copy)
QGXBDMJGAMFCBF-HLUDHZFRSA-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/h12-16,20H,3-11H2,1-2H3/t12-,13+,14-,15-,16-,18-,19-/m0/s1
SMILES (Click to copy)
C1[C@@H](O)C[C@]2([H])CC[C@@]3([H])[C@]4([H])CCC(=O)[C@@]4(C)CC[C@]3([H])[C@@]2(C)C1
Other Databases
Wikipedia
KEGG ID
HMDB ID
CHEBI ID
LIPIDBANK ID
SST0002
PubChem CID
SwissLipids ID
Cayman ID
PDB ID
BMRB ID(NMR)
NP-MRD ID(NMR)
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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Updated at
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