Identification

PhytoHub ID
PHUB002996
Name
4 '-Demethyltangeretin
Systematic Name
Not Available
Synonyms
Not Available
CAS Number
Not Available
Average Mass
358.346
Monoisotopic Mass
358.10525292
Chemical Formula
C19H18O7
IUPAC Name
Not Available
InChI Key
IECRXMSGDFIOEY-UHFFFAOYSA-N
InChI Identifier
InChI=1S/C19H18O7/c1-22-15-14-12(21)9-13(10-5-7-11(20)8-6-10)26-16(14)18(24-3)19(25-4)17(15)23-2/h5-9,20H,1-4H3
SMILES
COC1=C(OC)C(OC)=C2C(=O)C=C(OC2=C1OC)C1=CC=C(O)C=C1
Structure

Calculated Properties

Solubility (ALOGPS)
Not Available
LogS (ALOGPS)
Not Available
LogP (ALOGPS)
Not Available
Hydrogen Acceptors
Not Available
Hydrogen Donors
Not Available
Rotatable Bond Count
Not Available
Polar Surface Area
Not Available
Refractivity
Not Available
Polarizability
Not Available
Formal Charge
Not Available
Physiological Charge
Not Available
pKa (strongest basic)
Not Available
pKa (strongest acidic)
Not Available
Number of Rings
Not Available
Rule of Five
No
Bioavailability
No
Ghose Filter
No
Veber's Rule
No
MDDR-like Rule
No

Taxonomy as Metabolite

Family
(Poly)phenol metabolites
Class
Flavonoid metabolites
Sub-class
Flavones (parent and host metabolites)

Taxonomy of its Food Phytochemical Precursor(s)

Food PhytochemicalFamilyClassSub-class
TangeretinPolyphenolsFlavonoidsFlavonesShow Food Phytochemical

Spectra from Phytohub

Spectrum TypeInstrument TypeIon ModeCollision Energy LevelViewPeaks
Predicted GC-MSGC-MSPositiveNot AvailableView Spectrum(94.04131312,0.9831741073);(105.0334885,1.180212203);(118.0413131,2.484261708);(119.0491377,3.773353765);(144.020578,0.960937359);(145.0284026,1.095363298);(146.0362272,0.8661892904);(147.0440518,1.029472731);(196.073003,1.934761642);(197.0808276,0.8490153525);(238.0835663,0.9763933201);(272.0679171,3.439165035);(273.0757417,3.517054083);(274.0835663,1.764959678);(275.0913909,0.941284021);(313.0706558,1.511073591);(316.0941296,1.381871936);(326.0784804,3.449771556);(327.086305,3.723079567);(328.0941296,6.045066851);(329.0975285,1.246131779);(329.1019542,3.322277585);(330.1097788,4.267998782);(331.1131818,0.8810870598);(340.0941296,1.345041117);(341.1019542,1.570314268);(342.0733945,3.144897885);(343.0812191,4.42454103);(344.0846174,0.9130711264);(357.0968683,0.898490691);(358.1046929,3.065388976)
Predicted GC-MSGC-MSPositiveNot AvailableView Spectrum(73.04679982,5.94244742);(175.0573631,1.526243129);(189.0730123,0.7234517332);(190.0808369,0.8435434807);(191.0886615,1.199693474);(196.073003,1.075447501);(197.0808276,1.059874738);(239.0550066,0.7247521388);(241.0706558,1.175910571);(327.086305,0.8038581276);(329.0839671,1.789984229);(329.1019542,1.974561015);(331.0996163,0.8109391377);(344.1074409,1.515572951);(345.1152655,0.9951338872);(346.1230901,0.9765424918);(357.0968683,1.921848995);(358.1046929,2.010792747);(359.1125175,0.9260235189);(385.1101796,1.410211239);(387.1258288,0.8339513832);(398.1180042,1.514365983);(399.1258288,1.723505317);(400.1336534,2.784907986);(401.1363938,0.8119580109);(401.141478,1.032460147);(402.1493026,1.704991361);(414.1129183,2.084719334);(415.1207429,8.142676051);(416.1234834,2.375881221);(430.1442167,1.258401168)
Predicted GC-MSGC-MSEiNot AvailableView Spectrum(94.04131312,0.9831741073);(105.0334885,1.180212203);(118.0413131,2.484261708);(119.0491377,3.773353765);(144.020578,0.960937359);(145.0284026,1.095363298);(146.0362272,0.8661892904);(147.0440518,1.029472731);(196.073003,1.934761642);(197.0808276,0.8490153525);(238.0835663,0.9763933201);(272.0679171,3.439165035);(273.0757417,3.517054083);(274.0835663,1.764959678);(275.0913909,0.941284021);(313.0706558,1.511073591);(316.0941296,1.381871936);(326.0784804,3.449771556);(327.086305,3.723079567);(328.0941296,6.045066851);(329.0975285,1.246131779);(329.1019542,3.322277585);(330.1097788,4.267998782);(331.1131818,0.8810870598);(340.0941296,1.345041117);(341.1019542,1.570314268);(342.0733945,3.144897885);(343.0812191,4.42454103);(344.0846174,0.9130711264);(357.0968683,0.898490691);(358.1046929,3.065388976)
Predicted LC-MS/MSNot AvailablePositivelowView Spectrum(327.0863146,5.546056261);(329.1019647,2.010898154);(331.1176147,1.112391691);(341.1019647,12.66403592);(343.0812292,1.780911047);(359.1125294,69.56697455)
Predicted LC-MS/MSNot AvailablePositivemedView Spectrum(265.0706646,4.072650869);(315.0863146,2.508572408);(317.1019647,2.173677455);(327.0863146,9.87165069);(329.1019647,3.726525266);(331.1176147,5.207870929);(341.1019647,13.58989673);(343.0812292,3.047154617);(359.1125294,37.37852179)
Predicted LC-MS/MSNot AvailablePositivehighView Spectrum(41.00219107,2.647802457);(63.02292652,2.894363974);(65.03857658,1.298430805);(77.00219107,7.145661754);(77.03857658,1.024049065);(79.01784114,1.640723377);(91.01784114,1.274817545);(93.0334912,1.608373309);(105.0334912,2.108284201);(117.0334912,3.023848691);(121.0284058,3.301703049);(135.0440559,1.746683738);(145.0284058,3.432884558);(161.0233204,5.169029802);(197.0808353,1.337153544);(213.0757499,1.220018733);(235.0600999,2.146936496);(239.0550145,1.020565584);(259.0600999,0.9955575388);(265.0706646,1.341550635);(273.0757499,1.366160842);(297.0757499,1.596689584);(299.0914,2.267285848);(311.0914,4.058242361);(313.0706646,4.981574592);(313.1070501,1.875548801);(315.0863146,4.062655788);(327.0863146,2.13084425);(331.1176147,1.854675872);(341.1019647,1.837763783);(343.0812292,2.239317179)
Predicted LC-MS/MSNot AvailableNegativelowView Spectrum(93.03458836,1.755111547);(239.0561117,0.6241953348);(327.0874118,2.205463281);(329.1030618,0.9872924016);(331.0823264,0.3308761719);(357.0979765,92.7458504)
Predicted LC-MS/MSNot AvailableNegativemedView Spectrum(41.00328823,2.665164295);(93.03458836,2.544030185);(273.0768471,3.510836496);(327.0874118,10.95915135);(329.1030618,3.444759558);(357.0979765,65.75085782)
Predicted LC-MS/MSNot AvailableNegativehighView Spectrum(41.00328823,1.968216957);(55.0189383,2.508241876);(85.02950298,29.44250255);(93.03458836,3.76792253);(109.029503,1.187919786);(117.0345884,3.063443057);(119.0138529,2.258071365);(145.029503,1.431852943);(155.0349823,1.312274971);(161.0244176,1.104221249);(187.0400677,2.101922478);(217.0506323,1.880251621);(231.0662824,1.095709736);(241.0506323,2.835078807);(243.0662824,5.176425772);(257.045547,9.30586376);(273.0768471,6.147908517);(297.0768471,2.05722686);(327.0874118,1.785905102)
Predicted LC-MS/MSNot AvailablePositivelowView Spectrum(359.11252,100.0)
Predicted LC-MS/MSNot AvailablePositivemediumView Spectrum(316.09413,1.0);(344.08905,11.0);(359.11252,100.0)
Predicted LC-MS/MSNot AvailablePositivehighView Spectrum(77.03857,5.0);(91.05422,8.0);(119.04914,14.0);(137.02332,10.0);(150.03114,16.0);(151.03897,22.0);(253.07121,4.0);(285.07574,85.0);(316.09413,100.0);(343.08122,47.0);(344.08905,35.0);(359.11252,15.0)
Predicted LC-MS/MSNot AvailableNegativelowView Spectrum(342.07449,5.0);(357.09797,100.0)
Predicted LC-MS/MSNot AvailableNegativemediumView Spectrum(239.0561,10.0);(314.07958,69.0);(342.07449,55.0);(357.09797,100.0)

Food Sources

No food source information available

Food Sources of its Food Phytochemical(s)

No food source information available of its precursor(s)

Role as Biomarker of intake

No roles as Biomarker of intake found

Metabolism

Food PhytochemicalMetaboliteSpeciesBiofluidsOriginTMaxCMaxUrinary ExcretionFormulaMonoisotopic mass
Tangeretin 4 '-DemethyltangeretinNot Availableurinehost-gut microbiota co-metaboliteNo data>20µmol/LNo dataC19H18O7358.10525292 Publications

Inter-Individual Variations in Metabolism

Food PhytochemicalMetaboliteEffectValue
Back