Identification

PhytoHub ID
PHUB001523
Name
Pinostilbene
Systematic Name
Not Available
Synonyms
  • 3-[(E)-2-(4-hydroxyphenyl)ethenyl]-5-methoxyphenol
  • 3-methoxy-4',5-dihydroxy-trans-stilbene
  • 3-methoxyresveratrol
  • 3,4'-dihydroxy-5-methoxystilbene
  • Resveratrol monomethyl ether
CAS Number
Not Available
Average Mass
242.274
Monoisotopic Mass
242.094294311
Chemical Formula
C15H14O3
IUPAC Name
3-[(1E)-2-(4-hydroxyphenyl)ethenyl]-5-methoxyphenol
InChI Key
KUWZXOMQXYWKBS-NSCUHMNNSA-N
InChI Identifier
InChI=1S/C15H14O3/c1-18-15-9-12(8-14(17)10-15)3-2-11-4-6-13(16)7-5-11/h2-10,16-17H,1H3/b3-2+
SMILES
COC1=CC(\C=C\C2=CC=C(O)C=C2)=CC(O)=C1
Structure

Calculated Properties

Solubility (ALOGPS)
2.41e-02 g/l
LogS (ALOGPS)
-4.00
LogP (ALOGPS)
3.08
Hydrogen Acceptors
3
Hydrogen Donors
2
Rotatable Bond Count
3
Polar Surface Area
49.69
Refractivity
71.93780000000001
Polarizability
26.569004865120604
Formal Charge
0
Physiological Charge
0
pKa (strongest basic)
-4.838664480653452
pKa (strongest acidic)
8.635714115937514
Number of Rings
2
Rule of Five
Yes
Bioavailability
Yes
Ghose Filter
Yes
Veber's Rule
No
MDDR-like Rule
No

Taxonomy as Metabolite

Family
(Poly)phenol metabolites
Class
Stilbene metabolites
Sub-class
Not Available

Taxonomy of its Food Phytochemical Precursor(s)

Food PhytochemicalFamilyClassSub-class
PterostilbenePolyphenolsStilbenesNot AvailableShow Food Phytochemical

Classyfire Taxonomy

Kingdom Name
Organic compounds
Class
Stilbenes
Super-class
Phenylpropanoids and polyketides
Sub-class
Not Available
Direct Parent Name
Stilbenes
Alternative Parent Names
["1-hydroxy-2-unsubstituted benzenoids", "1-hydroxy-4-unsubstituted benzenoids", "Alkyl aryl ethers", "Anisoles", "Hydrocarbon derivatives", "Methoxybenzenes", "Methoxyphenols", "Phenoxy compounds", "Styrenes"]
External Descriptor Annotations
["stilbenol"]
Substituent Names
["1-hydroxy-2-unsubstituted benzenoid", "1-hydroxy-4-unsubstituted benzenoid", "Alkyl aryl ether", "Anisole", "Aromatic homomonocyclic compound", "Benzenoid", "Ether", "Hydrocarbon derivative", "Methoxybenzene", "Methoxyphenol", "Monocyclic benzene moiety", "Organic oxygen compound", "Organooxygen compound", "Phenol", "Phenol ether", "Phenoxy compound", "Stilbene", "Styrene"]

Spectra from Phytohub

Spectrum TypeInstrument TypeIon ModeCollision Energy LevelViewPeaks
Predicted LC-MS/MSNot AvailablePositivelowView Spectrum(105.0334912,7.861837409);(107.0491413,3.934659258);(137.0597059,3.934266131);(211.075356,3.737003994);(225.0910061,3.011710722);(243.1015708,60.73605392)
Predicted LC-MS/MSNot AvailablePositivemedView Spectrum(105.0334912,17.86035343);(107.0491413,6.721253003);(117.0334912,1.707626791);(119.0491413,4.389941954);(123.0440559,2.691756984);(137.0597059,7.0065529);(143.0491413,1.256534154);(147.0440559,1.406761421);(149.0597059,4.029840007);(199.075356,2.651115263);(201.0910061,1.809262456);(211.075356,3.309095743);(213.0910061,2.150335031);(215.1066561,2.322252461);(225.0910061,2.479025172);(243.1015708,18.23352082)
Predicted LC-MS/MSNot AvailablePositivehighView Spectrum(39.02292652,1.160003846);(49.00727645,1.094084802);(65.03857658,1.840920619);(75.02292652,3.131424333);(77.03857658,6.618627022);(79.01784114,1.808973944);(79.05422664,2.438301843);(81.0334912,2.457355591);(89.03857658,1.028496213);(91.05422664,1.032744422);(95.04914126,2.783002707);(101.0385766,1.002831985);(105.0334912,9.48996927);(107.0491413,4.640096928);(117.0334912,2.777054598);(119.0491413,2.032111755);(121.0647913,1.27316063);(123.0440559,2.476201848);(137.0597059,3.864578706);(141.0334912,1.789213488);(143.0491413,2.739031598);(147.0440559,0.9630194047);(169.0647913,1.031281792);(181.0647913,1.218741141);(183.0804414,2.954524241);(185.0597059,1.447882361);(187.075356,1.381704406);(199.075356,3.145338449);(201.0910061,1.918921622);(211.075356,1.59571429);(227.0702706,1.877182252)
Predicted LC-MS/MSNot AvailableNegativelowView Spectrum(209.0608031,1.277122234);(211.0764532,1.187174874);(213.0921032,1.641395807);(223.0764532,0.7176773521);(225.0557177,1.033980649);(241.0870179,91.20479207)
Predicted LC-MS/MSNot AvailableNegativemedView Spectrum(197.0608031,3.709367632);(199.0764532,3.619290748);(211.0764532,3.155722059);(213.0921032,6.945502793);(225.0557177,10.63074073);(241.0870179,52.84587593)
Predicted LC-MS/MSNot AvailableNegativehighView Spectrum(41.00328823,2.93416879);(55.0189383,6.926808212);(93.03458836,2.725522593);(105.0345884,2.778530582);(141.0345884,1.616971843);(143.0502384,1.977793864);(157.0658885,6.637371044);(167.0502384,1.832268385);(169.0658885,1.886468919);(181.0658885,6.096930706);(183.045153,5.045714681);(183.0815386,4.370443567);(185.0608031,2.33934648);(193.0658885,1.252962744);(197.0608031,6.534455066);(199.0764532,2.091390145);(209.0608031,2.303547058);(211.0764532,3.543477743);(213.0921032,3.903976676);(225.0557177,13.92983558)

Food Sources

No food source information available

Food Sources of its Food Phytochemical(s)

Role as Biomarker of intake

No roles as Biomarker of intake found

Metabolism

Food PhytochemicalMetaboliteSpeciesBiofluidsOriginTMaxCMaxUrinary ExcretionFormulaMonoisotopic mass
Pterostilbene Pinostilbenemousecolon tissue, colonic contenthost metabolismNot AvailableNot AvailableNot AvailableC15H14O3242.094294311 Publications

Inter-Individual Variations in Metabolism

Food PhytochemicalMetaboliteEffectValue
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