Record Information
Version1.0
Creation Date2016-09-30 23:01:17 UTC
Update Date2020-04-22 15:11:17 UTC
BMDB IDBMDB0002697
Secondary Accession Numbers
  • BMDB02697
Metabolite Identification
Common Name19-Norandrosterone
Description19-Norandrosterone, also known as 19-noretiocholanolone, belongs to the class of organic compounds known as estrogens and derivatives. These are steroids with a structure containing a 3-hydroxylated estrane. Thus, 19-norandrosterone is considered to be a steroid. Based on a literature review a significant number of articles have been published on 19-Norandrosterone.
Structure
Thumb
Synonyms
ValueSource
19-NoreoiandrosteroneChEBI
19-NoretiocholanoloneChEBI
3-Hydroxyestran-17-oneHMDB
19-Norandrosterone, (3alpha,5alpha)-isomerHMDB
(3alpha,5alpha)-3-Hydroxyestran-17-oneHMDB
(3Α,5α)-3-hydroxyestran-17-oneHMDB
3alpha-Hydroxy-5alpha-estran-17-oneHMDB
3Α-hydroxy-5α-estran-17-oneHMDB
5alpha-Estran-3alpha-ol-17-oneHMDB
5Α-estran-3α-ol-17-oneHMDB
19-NorandrosteroneHMDB
Chemical FormulaC18H28O2
Average Molecular Weight276.42
Monoisotopic Molecular Weight276.208930142
IUPAC Name(1R,2S,5R,7S,10R,11S,15S)-5-hydroxy-15-methyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-14-one
Traditional Name(1R,2S,5R,7S,10R,11S,15S)-5-hydroxy-15-methyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-14-one
CAS Registry Number1225-01-0
SMILES
[H][C@@]12CCC(=O)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])CC[C@@]2([H])C[C@H](O)CC[C@]12[H]
InChI Identifier
InChI=1S/C18H28O2/c1-18-9-8-14-13-5-3-12(19)10-11(13)2-4-15(14)16(18)6-7-17(18)20/h11-16,19H,2-10H2,1H3/t11-,12+,13-,14+,15+,16-,18-/m0/s1
InChI KeyUOUIARGWRPHDBX-CQZDKXCPSA-N
Chemical Taxonomy
Description belongs to the class of organic compounds known as estrogens and derivatives. These are steroids with a structure containing a 3-hydroxylated estrane.
KingdomOrganic compounds
Super ClassLipids and lipid-like molecules
ClassSteroids and steroid derivatives
Sub ClassEstrane steroids
Direct ParentEstrogens and derivatives
Alternative Parents
Substituents
  • Estrogen-skeleton
  • 3-hydroxysteroid
  • Hydroxysteroid
  • 3-alpha-hydroxysteroid
  • 17-oxosteroid
  • Oxosteroid
  • Cyclic alcohol
  • Ketone
  • Secondary alcohol
  • Organooxygen compound
  • Hydrocarbon derivative
  • Organic oxide
  • Organic oxygen compound
  • Carbonyl group
  • Alcohol
  • Aliphatic homopolycyclic compound
Molecular FrameworkAliphatic homopolycyclic compounds
External Descriptors
Ontology
StatusExpected but not Quantified
Origin
  • Endogenous
  • Exogenous
BiofunctionNot Available
ApplicationNot Available
Cellular locations
  • Cell membrane
  • Cytoplasm
  • Membrane
Physical Properties
StateSolid
Experimental Properties
PropertyValueReference
Melting Point162 - 163 °CNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogP3.887Not Available
Predicted Properties
PropertyValueSource
logP3.34ALOGPS
logP3.47ChemAxon
logS-4.4ALOGPS
pKa (Strongest Acidic)18.31ChemAxon
pKa (Strongest Basic)-1.4ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count2ChemAxon
Hydrogen Donor Count1ChemAxon
Polar Surface Area37.3 ŲChemAxon
Rotatable Bond Count0ChemAxon
Refractivity79.33 m³·mol⁻¹ChemAxon
Polarizability32.94 ųChemAxon
Number of Rings4ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleYesChemAxon
MDDR-like RuleYesChemAxon
Spectra
Spectra
Spectrum TypeDescriptionSplash Key
Predicted GC-MSPredicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, PositiveNot AvailableView in JSpectraViewer
Predicted GC-MSPredicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, PositiveNot AvailableView in JSpectraViewer
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-004i-0090000000-7c08ae4a5c8bc21486d6View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-0zi1-2980000000-16396bb89df457c641e7View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-0ktb-2900000000-ee34ac41106cf13a9a3dView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-004i-0090000000-4d3066b364d5c97a28e0View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-004i-0090000000-4d3066b364d5c97a28e0View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-00fr-0090000000-e73157a0418447ebbe85View in MoNA
Biological Properties
Cellular Locations
  • Cell membrane
  • Cytoplasm
  • Membrane
Biospecimen LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
HMDB IDHMDB0002697
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB023046
KNApSAcK IDNot Available
Chemspider ID7827676
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia Link19-Norandrosterone
METLIN IDNot Available
PubChem Compound9548753
PDB IDNot Available
ChEBI ID36412
References
Synthesis ReferenceCaglioti, L.; Cainelli, G.; Maina, G.; Selva, A. Hydroboration. V. New synthesis of androsterone and 19-norandrosterone. Tetrahedron (1964), 20(4), 957-61.
Material Safety Data Sheet (MSDS)Not Available
General ReferencesNot Available