Record Information
Version1.0
Creation Date2016-09-30 22:37:55 UTC
Update Date2020-06-04 20:48:42 UTC
BMDB IDBMDB0000876
Secondary Accession Numbers
  • BMDB00876
Metabolite Identification
Common NameVitamin D3
DescriptionVitamin D3 belongs to the class of organic compounds known as vitamin d and derivatives. Vitamin D and derivatives are compounds containing a secosteroid backbone, usually secoergostane or secocholestane. Vitamin D3 is an extremely weak basic (essentially neutral) compound (based on its pKa).
Structure
Thumb
Synonyms
ValueSource
(+)-Vitamin D3HMDB
(3beta,Z,7E)-9,10-Secocholesta-5,7,10(19)-trien-3-olHMDB
(5E,7E)-9,10-Secocholesta-5,7,10-trien-3-olHMDB
3-beta,Z,7E-9,10-Secocholestr-5,7,10(19)-trien-3-olHMDB
9,10-Secocholesta-5,7,10(19)-trien-3-beta-olHMDB
9,10-Secocholesta-5,7,10(19)-trien-3-olHMDB
9,10-Secocholesta-5,7,10-trien-3-olHMDB
ArachitolHMDB
CalciolHMDB
CCHMDB
CholecalciferolHMDB
Cholecalciferol D3HMDB
ColecalciferolHMDB
D3-VigantolHMDB
DelsterolHMDB
DeparalHMDB
DevaronHMDB
EbivitHMDB
FeraColHMDB
Granuvit D3HMDB
micro-DeeHMDB
Oleovitamin D3HMDB
ProvitinaHMDB
QuintoxHMDB
RicketonHMDB
TrivitanHMDB
Vi-de3HMDB
VidDe-3-hydrosolHMDB
VidekholHMDB
VigantolHMDB
VigorsanHMDB
Vitinc dan-dee-3HMDB
(3 beta,5Z,7E)-9,10-Secocholesta-5,7,10(19)-trien-3-olMeSH
CholecalciferolsMeSH
Vitamin D 3MeSH
Chemical FormulaC27H44O
Average Molecular Weight384.6377
Monoisotopic Molecular Weight384.33921603
IUPAC Name(1S,3Z)-3-{2-[(1R,4E,7aR)-7a-methyl-1-[(2R)-6-methylheptan-2-yl]-octahydro-1H-inden-4-ylidene]ethylidene}-4-methylidenecyclohexan-1-ol
Traditional Namerampage
CAS Registry Number67-97-0
SMILES
CC(C)CCC[C@@H](C)[C@H]1CCC2\C(CCC[C@]12C)=C\C=C1\C[C@@H](O)CCC1=C
InChI Identifier
InChI=1S/C27H44O/c1-19(2)8-6-9-21(4)25-15-16-26-22(10-7-17-27(25,26)5)12-13-23-18-24(28)14-11-20(23)3/h12-13,19,21,24-26,28H,3,6-11,14-18H2,1-2,4-5H3/b22-12+,23-13-/t21-,24+,25-,26?,27-/m1/s1
InChI KeyQYSXJUFSXHHAJI-QWSSABAFSA-N
Chemical Taxonomy
Description belongs to the class of organic compounds known as vitamin d and derivatives. Vitamin D and derivatives are compounds containing a secosteroid backbone, usually secoergostane or secocholestane.
KingdomOrganic compounds
Super ClassLipids and lipid-like molecules
ClassSteroids and steroid derivatives
Sub ClassVitamin D and derivatives
Direct ParentVitamin D and derivatives
Alternative Parents
Substituents
  • Triterpenoid
  • Cyclic alcohol
  • Secondary alcohol
  • Organic oxygen compound
  • Hydrocarbon derivative
  • Organooxygen compound
  • Alcohol
  • Aliphatic homopolycyclic compound
Molecular FrameworkAliphatic homopolycyclic compounds
External DescriptorsNot Available
Ontology
StatusDetected and Quantified
Origin
  • Endogenous
  • Exogenous
BiofunctionNot Available
ApplicationNot Available
Cellular locations
  • Cell membrane
  • Cytoplasm
  • Membrane
  • Mitochondria
Physical Properties
StateSolid
Experimental Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Predicted Properties
PropertyValueSource
logP7.98ALOGPS
logP7.13ChemAxon
logS-6ALOGPS
pKa (Strongest Acidic)18.38ChemAxon
pKa (Strongest Basic)-1.3ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count1ChemAxon
Hydrogen Donor Count1ChemAxon
Polar Surface Area20.23 ŲChemAxon
Rotatable Bond Count6ChemAxon
Refractivity123.22 m³·mol⁻¹ChemAxon
Polarizability49.44 ųChemAxon
Number of Rings3ChemAxon
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, Positivesplash10-0aou-3029000000-1950c74de34369a70400View in MoNA
Predicted GC-MSPredicted GC-MS Spectrum - GC-MS (1 TMS) - 70eV, Positivesplash10-002f-9207800000-c6f808a014153de38d58View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-014r-0129000000-442693b5a55274aeb0b3View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-0c09-3496000000-bf01a7ddf350733d39f2View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-0a4i-8298000000-b9136b2dd6e2c22c1123View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-001i-0009000000-70ba08bf3cd328c6087eView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-001i-0009000000-c16445787a057993951aView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-066r-1239000000-328f37347d493ff8f54aView in MoNA
1D NMR1H NMR Spectrum (1D, 600 MHz, CDCl3, experimental)Not AvailableView in JSpectraViewer
2D NMR[1H, 13C]-HSQC NMR Spectrum (2D, 600 MHz, CDCl3, experimental)Not AvailableView in JSpectraViewer
Biological Properties
Cellular Locations
  • Cell membrane
  • Cytoplasm
  • Membrane
  • Mitochondria
Biospecimen Locations
  • Epidermis
  • Fibroblasts
  • Intestine
  • Kidney
  • Liver
  • Milk
  • Ovary
  • Placenta
  • Prostate Tissue
  • Spleen
  • Testis
Pathways
Normal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
EpidermisExpected but not QuantifiedNot QuantifiedNot SpecifiedNot SpecifiedNormal
  • Not Applicable
details
FibroblastsExpected but not QuantifiedNot QuantifiedNot SpecifiedNot SpecifiedNormal
  • Not Applicable
details
IntestineExpected but not QuantifiedNot QuantifiedNot SpecifiedNot SpecifiedNormal
  • Not Applicable
details
KidneyExpected but not QuantifiedNot QuantifiedNot SpecifiedNot SpecifiedNormal
  • Not Applicable
details
LiverExpected but not QuantifiedNot QuantifiedNot SpecifiedNot SpecifiedNormal
  • Not Applicable
details
MilkDetected and Quantified0.00013 uMNot SpecifiedNot Specified
Normal
details
MilkDetected and Quantified0.00013 uMNot SpecifiedNot Specified
Normal
details
MilkDetected and Quantified0.000182 uMNot SpecifiedNot Specified
Normal
details
MilkDetected and Quantified0.00198 uMNot SpecifiedNot Specified
Normal
details
MilkDetected and Quantified0.000182 uMNot SpecifiedNot Specified
Normal
details
MilkDetected and Quantified0.0026 uMNot SpecifiedNot Specified
Normal
details
MilkDetected and Quantified0.000234 uMNot SpecifiedNot Specified
Normal
details
MilkDetected and Quantified0.000208 uMNot SpecifiedNot Specified
Normal
details
MilkDetected and Quantified0.0147 +/- 0.0002 uMNot SpecifiedNot Specified
Normal
details
MilkDetected and Quantified0.019 +/- 0.001 uMNot SpecifiedNot Specified
Normal
details
MilkDetected and Quantified0.0435 +/- 0.0002 uMNot SpecifiedNot Specified
Normal
details
MilkDetected and Quantified0.015 +/- 0.001 uMNot SpecifiedNot Specified
Normal
details
MilkDetected and Quantified0.00052 uMNot SpecifiedNot SpecifiedNormal
    • Pirjo H. Mattila,...
details
OvaryExpected but not QuantifiedNot QuantifiedNot SpecifiedNot SpecifiedNormal
  • Not Applicable
details
PlacentaExpected but not QuantifiedNot QuantifiedNot SpecifiedNot SpecifiedNormal
  • Not Applicable
details
Prostate TissueExpected but not QuantifiedNot QuantifiedNot SpecifiedNot SpecifiedNormal
  • Not Applicable
details
SpleenExpected but not QuantifiedNot QuantifiedNot SpecifiedNot SpecifiedNormal
  • Not Applicable
details
TestisExpected but not QuantifiedNot QuantifiedNot SpecifiedNot SpecifiedNormal
  • Not Applicable
details
Abnormal Concentrations
Not Available
HMDB IDHMDB0014315
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDNot Available
KNApSAcK IDNot Available
Chemspider IDNot Available
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkCholecalciferol
METLIN IDNot Available
PubChem Compound10883523
PDB IDNot Available
ChEBI IDNot Available
References
Synthesis ReferenceNemoto, Hideo; Kurobe, Hiroshi; Fukumoto, Keiichiro; Kametani, Tetsuji. A modified synthesis of the (+)-8a-phenylsulfonyl-des-AB-cholestane via an intramolecular nucleophilic attack to epoxide - a total synthesis of vitamin D3. Heterocycles (1985), 23(3),
Material Safety Data Sheet (MSDS)Not Available
General References
  1. A. Foroutan et al. (2019). A. Foroutan et al. The Chemical Composition of Commercial Cow's Milk (in preparation). Journal of Agricultural and Food Chemistry.
  2. Pirjo H. Mattila, Vieno I. Piironen, Esko J. Uusi-Rauva, and Pekka E. Koivistoinen (1995). Pirjo H. Mattila, Vieno I. Piironen, Esko J. Uusi-Rauva, and Pekka E. Koivistoinen. 1995. Contents of Cholecalciferol, Ergocalciferol, and Their 25-Hydroxylated Metabolites in Milk Products and Raw Meat and Liver As Determined by HPLC. J. Agric. Food Chem. 43 (9), pp 2394–2399. J. Agric. Food Chem.
  3. Fooddata+, The Technical University of Denmark (DTU) [Link]

Enzymes

General function:
Involved in sequence-specific DNA binding
Specific function:
Nuclear receptor for calcitriol, the active form of vitamin D3 which mediates the action of this vitamin on cells (By similarity). Enters the nucleus upon vitamin D3 binding where it forms heterodimers with the retinoid X receptor/RXR (By similarity). The VDR-RXR heterodimers bind to specific response elements on DNA and activate the transcription of vitamin D3-responsive target genes (By similarity). Plays a central role in calcium homeostasis (By similarity).
Gene Name:
VDR
Uniprot ID:
Q28037
Molecular weight:
48318.0
General function:
Involved in steroid hormone receptor activity
Specific function:
Not Available
Gene Name:
VDR
Uniprot ID:
Q19MM0
Molecular weight:
6042.0