PhytoHub: Showing entry for 7-Hydroxymatairesinol

7-Hydroxymatairesinol

Identification

PhytoHub ID

PHUB001696

Name

7-Hydroxymatairesinol

Systematic Name

Not Available

Synonyms

Not Available

CAS Number

Not Available

Average Mass

374.389

Monoisotopic Mass

374.136553048

Chemical Formula

C₂₀H₂₂O₇

IUPAC Name

(4R)-3-[(S)-hydroxy(4-hydroxy-3-methoxyphenyl)methyl]-4-[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one

InChI Key

ZZSOKNNVDKKSDE-LPHKOSDUSA-N

InChI Identifier

InChI=1S/C20H22O7/c1-25-16-8-11(3-5-14(16)21)7-13-10-27-20(24)18(13)19(23)12-4-6-15(22)17(9-12)26-2/h3-6,8-9,13,18-19,21-23H,7,10H2,1-2H3/t13-,18?,19+/m0/s1

SMILES

COC1=CC(C[C@H]2COC(=O)C2[C@H](O)C2=CC=C(O)C(OC)=C2)=CC=C1O

Structure

Similar Structures

Calculated Properties

Solubility (ALOGPS): 3.67e-02 g/l
LogS (ALOGPS): -4.01
LogP (ALOGPS): 2.00
Hydrogen Acceptors: 6
Hydrogen Donors: 3
Rotatable Bond Count: 6
Polar Surface Area: 105.45000000000002
Refractivity: 96.9959
Polarizability: 37.32908214360327
Formal Charge: 0
Physiological Charge: 0
pKa (strongest basic): -3.2736705554452006
pKa (strongest acidic): 9.626846763883268
Number of Rings: 3
Rule of Five: Yes
Bioavailability: Yes
Ghose Filter: Yes
Veber's Rule: No
MDDR-like Rule: Yes

External Links

No external links

Taxonomy as Food Phytochemical

Family: Polyphenols
Class: Lignans
Sub-class: Not Available

Classyfire Taxonomy

Kingdom Name: Organic compounds
Class: Furanoid lignans
Super-class: Lignans, neolignans and related compounds
Sub-class: Tetrahydrofuran lignans
Direct Parent Name: Dibenzylbutyrolactone lignans
Alternative Parent Names: ["1-hydroxy-2-unsubstituted benzenoids", "Alkyl aryl ethers", "Anisoles", "Aromatic alcohols", "Carbonyl compounds", "Carboxylic acid esters", "Gamma butyrolactones", "Hydrocarbon derivatives", "Lignan lactones", "Methoxybenzenes", "Methoxyphenols", "Monocarboxylic acids and derivatives", "Organic oxides", "Oxacyclic compounds", "Phenoxy compounds", "Secondary alcohols", "Tetrahydrofurans"]
External Descriptor Annotations: Not Available
Substituent Names: ["1-hydroxy-2-unsubstituted benzenoid", "Alcohol", "Alkyl aryl ether", "Anisole", "Aromatic alcohol", "Aromatic heteromonocyclic compound", "Benzenoid", "Carbonyl group", "Carboxylic acid derivative", "Carboxylic acid ester", "Dibenzylbutyrolactone", "Ether", "Gamma butyrolactone", "Hydrocarbon derivative", "Lactone", "Lignan lactone", "Methoxybenzene", "Methoxyphenol", "Monocarboxylic acid or derivatives", "Monocyclic benzene moiety", "Organic oxide", "Organic oxygen compound", "Organoheterocyclic compound", "Organooxygen compound", "Oxacycle", "Phenol", "Phenol ether", "Phenoxy compound", "Secondary alcohol", "Tetrahydrofuran"]

Spectra from Phytohub

Spectrum Type	Instrument Type	Ion Mode	Collision Energy Level	View	Peaks

Predicted LC-MS/MS	Not Available	Positive	low	View Spectrum	(125.0602545,0.4590401261);(137.0602545,1.931175661);(149.0602545,1.338475216);(151.0395191,1.275129929);(153.0551691,11.43909042);(155.0708192,0.6630357762);(161.0602545,1.297039884);(163.0759046,4.060712135);(219.0657338,1.014183072);(221.0813839,2.439880974);(223.097034,0.5859267899);(231.0657338,1.130670098);(233.0813839,2.232460834);(237.0762985,0.6624294224);(249.0762985,0.5713455975);(251.0919486,2.757260729);(295.097034,0.5551287498);(311.1283341,1.063110416);(313.1439842,0.9744621818);(325.1075986,1.565830654);(327.1232487,1.217012368);(329.1388988,0.6941232219);(331.1545488,0.4796172258);(339.1232487,0.4725158871);(339.1232487,1.377465888);(341.1025133,0.4800102107);(343.1181633,1.911427173);(345.1338134,0.8821928286);(357.1338134,1.045587675);(357.1338134,26.84844881);(375.1443781,26.57521005)
Predicted LC-MS/MS	Not Available	Positive	med	View Spectrum	(121.0289544,1.816395862);(123.0446045,2.084943061);(131.0496898,1.785141922);(137.0602545,6.04483578);(149.0602545,1.383762191);(151.0395191,1.733355434);(153.0551691,19.15753161);(161.0602545,4.529611227);(163.0759046,6.660278351);(165.0915547,1.896749208);(219.0657338,2.060081335);(221.0813839,1.594140808);(231.0657338,1.673986015);(233.0813839,4.763129316);(237.0762985,1.261685313);(249.0762985,1.201880402);(251.0919486,4.46860247);(295.097034,2.199258677);(297.112684,1.40838298);(309.112684,1.847982374);(311.1283341,1.324080158);(325.1075986,2.421279675);(327.1232487,2.485437169);(327.1232487,2.052935363);(331.1545488,1.602445092);(339.1232487,1.295767809);(343.1181633,1.159885164);(345.1338134,1.990314155);(357.1338134,1.077918379);(357.1338134,8.587687322);(375.1443781,6.430515375)
Predicted LC-MS/MS	Not Available	Positive	high	View Spectrum	(51.0234751,4.187989626);(77.03912516,4.76474816);(81.03403978,2.058614587);(83.01330434,1.576614326);(91.05477522,1.365910542);(107.0496898,2.102132105);(119.0496898,3.284464521);(121.0289544,4.213613119);(123.0446045,3.54238831);(131.0496898,1.369055454);(133.0653399,1.757182526);(137.023869,1.738826809);(137.0602545,6.976805106);(149.0602545,7.630301619);(151.0395191,7.253848782);(151.0759046,1.475138431);(153.0551691,8.293283028);(161.0602545,8.613277489);(163.0759046,5.716402427);(165.0915547,1.647738888);(175.0395191,1.71189461);(179.0708192,1.59465256);(183.1021193,1.392191113);(231.0657338,2.378621155);(233.0813839,1.602954587);(285.112684,1.699219442);(295.097034,1.847374992);(325.1075986,1.985256835);(327.1232487,2.284614206);(339.1232487,2.086784918);(341.1025133,1.848099727)
Predicted LC-MS/MS	Not Available	Negative	low	View Spectrum	(29.00273965,0.2543852135);(123.0446045,0.3451588019);(135.0446045,0.3688719489);(137.0602545,0.8363528687);(151.0395191,0.5206981615);(153.0551691,0.5663575163);(163.0759046,0.7780631858);(175.0759046,0.4557878307);(177.0915547,0.6682664134);(179.0708192,0.2613123553);(191.0708192,0.2244412694);(203.0708192,0.5727652422);(205.0500838,1.483430814);(209.0449984,0.2588901453);(217.0500838,0.2352448542);(219.0657338,1.202322932);(221.0813839,15.48128835);(223.097034,0.2048684994);(225.0762985,0.208564642);(237.0762985,0.8359184633);(311.1283341,0.4242456906);(325.1075986,0.5703469214);(327.1232487,0.2587269787);(329.1388988,2.714275071);(339.0868632,0.3471800264);(341.1025133,0.4950995053);(343.1181633,0.7020193207);(355.1181633,0.238535096);(355.1181633,10.87899048);(357.0974279,1.273503509);(373.128728,56.33408789)
Predicted LC-MS/MS	Not Available	Negative	med	View Spectrum	(85.0289544,1.632963245);(121.0289544,1.105882743);(123.0446045,1.887900134);(135.0446045,1.694319322);(137.023869,1.099968357);(137.0602545,1.824579482);(149.0602545,0.8622499589);(151.0395191,3.837259109);(153.0551691,1.902798434);(163.0759046,1.063498766);(165.0551691,2.465170824);(167.0708192,2.730693647);(175.0759046,1.224329599);(177.0915547,4.857852541);(179.0708192,1.326402431);(189.0551691,1.178090572);(191.0708192,1.740275331);(203.0708192,2.053928373);(205.0500838,8.099211305);(207.0657338,0.8731269377);(219.0657338,2.151570704);(221.0813839,16.31955755);(311.1283341,1.52805457);(313.1075986,3.200326627);(325.1075986,2.150127191);(327.1232487,2.800334244);(329.1388988,9.497791866);(343.1181633,1.28471631);(355.1181633,5.676105961);(357.0974279,3.475069104);(373.128728,8.455844764)
Predicted LC-MS/MS	Not Available	Negative	high	View Spectrum	(41.00273965,4.624558445);(83.01330434,1.292479681);(85.0289544,1.218303503);(97.0289544,1.354136976);(109.0289544,1.841225638);(121.0289544,2.868788758);(123.0446045,7.913111519);(137.023869,5.819048163);(139.0395191,1.1611462);(147.0446045,1.543300168);(149.023869,3.48006742);(149.0602545,2.344620245);(151.0395191,6.642052171);(153.0551691,5.780471532);(159.0446045,1.091368604);(161.0602545,1.754132816);(163.0759046,1.472563521);(165.0551691,4.059971849);(177.0915547,3.083355303);(179.0708192,2.347231503);(189.0551691,4.212168704);(191.0708192,6.469396981);(205.0500838,4.484933709);(205.0864693,1.406761425);(207.0657338,2.157551023);(221.0449984,2.533702303);(221.0813839,5.438496869);(313.1075986,1.982077633);(327.0868632,5.981726696);(343.1181633,2.308646924);(357.0974279,1.332603715)
Predicted LC-MS/MS	Not Available	Positive	low	View Spectrum	(121.02841,5.43);(121.02841,5.43);(123.04406,10.98);(123.04406,10.98);(123.04406,10.98);(123.04406,10.98);(123.04406,10.98);(123.04406,10.98);(125.05971,12.23);(125.05971,12.23);(125.05971,12.23);(135.04406,10.52);(135.04406,10.52);(135.04406,10.52);(137.05971,13.2);(137.05971,13.2);(137.05971,13.2);(137.05971,13.2);(137.05971,13.2);(153.05462,17.96);(153.05462,17.96);(153.05462,17.96);(153.05462,17.96);(153.05462,17.96);(153.05462,17.96);(223.09649,5.49);(223.09649,5.49);(223.09649,5.49);(223.09649,5.49);(223.09649,5.49);(223.09649,5.49);(223.09649,5.49);(233.08084,9.74);(233.08084,9.74);(233.08084,9.74);(233.08084,9.74);(249.07575,6.39);(249.07575,6.39);(249.07575,6.39);(251.0914,53.94);(251.0914,53.94);(251.0914,53.94);(251.0914,53.94);(251.0914,53.94);(251.0914,53.94);(251.0914,53.94);(251.0914,53.94);(251.0914,53.94);(251.0914,53.94);(251.0914,53.94);(251.0914,53.94);(251.0914,53.94);(251.0914,53.94);(251.0914,53.94);(343.11761,10.69);(343.11761,10.69);(343.11761,10.69);(343.11761,10.69);(343.11761,10.69);(343.11761,10.69);(347.14891,7.41);(347.14891,7.41);(347.14891,7.41);(347.14891,7.41);(347.14891,7.41);(347.14891,7.41);(357.13326,21.28);(357.13326,21.28);(357.13326,21.28);(357.13326,21.28);(357.13326,21.28);(357.13326,21.28);(357.13326,21.28);(357.13326,21.28);(375.14383,100.0);(375.14383,100.0);(375.14383,100.0);(375.14383,100.0);(375.14383,100.0);(375.14383,100.0);(375.14383,100.0);(375.14383,100.0);(375.14383,100.0);(375.14383,100.0);(375.14383,100.0);(375.14383,100.0);(375.14383,100.0);(375.14383,100.0);(375.14383,100.0);(375.14383,100.0);(375.14383,100.0)
Predicted LC-MS/MS	Not Available	Positive	medium	View Spectrum	(83.04914,12.23);(83.04914,12.23);(105.03349,9.84);(109.06479,15.97);(121.02841,35.55);(121.02841,35.55);(123.04406,23.91);(123.04406,23.91);(123.04406,23.91);(123.04406,23.91);(123.04406,23.91);(123.04406,23.91);(125.05971,73.37);(125.05971,73.37);(125.05971,73.37);(127.03897,22.02);(127.03897,22.02);(127.07536,28.65);(127.07536,28.65);(127.07536,28.65);(127.07536,28.65);(129.05462,23.22);(135.04406,100.0);(135.04406,100.0);(135.04406,100.0);(137.05971,85.53);(137.05971,85.53);(137.05971,85.53);(137.05971,85.53);(137.05971,85.53);(139.07536,17.26);(139.07536,17.26);(139.07536,17.26);(139.07536,17.26);(139.07536,17.26);(139.07536,17.26);(153.05462,29.9);(153.05462,29.9);(153.05462,29.9);(153.05462,29.9);(153.05462,29.9);(153.05462,29.9);(163.07536,7.19);(165.09101,8.68);(165.09101,8.68);(165.09101,8.68);(219.06519,14.68);(219.06519,14.68);(219.06519,14.68);(221.08084,18.54);(221.08084,18.54);(221.08084,18.54);(221.08084,18.54);(221.08084,18.54);(221.08084,18.54);(221.08084,18.54);(221.08084,18.54);(221.08084,18.54);(223.09649,12.72);(223.09649,12.72);(223.09649,12.72);(223.09649,12.72);(223.09649,12.72);(223.09649,12.72);(223.09649,12.72);(233.08084,20.44);(233.08084,20.44);(233.08084,20.44);(233.08084,20.44);(235.09649,16.36);(235.09649,16.36);(251.0914,56.09);(251.0914,56.09);(251.0914,56.09);(251.0914,56.09);(251.0914,56.09);(251.0914,56.09);(251.0914,56.09);(251.0914,56.09);(251.0914,56.09);(251.0914,56.09);(251.0914,56.09);(251.0914,56.09);(251.0914,56.09);(251.0914,56.09);(251.0914,56.09);(253.10705,12.8);(253.10705,12.8);(253.10705,12.8);(253.10705,12.8);(253.10705,12.8);(253.10705,12.8);(303.1227,13.36);(303.1227,13.36);(303.1227,13.36);(311.12779,6.87);(313.14344,10.48);(325.10705,7.2);(343.11761,11.96);(343.11761,11.96);(343.11761,11.96);(343.11761,11.96);(343.11761,11.96);(343.11761,11.96);(347.14891,14.61);(347.14891,14.61);(347.14891,14.61);(347.14891,14.61);(347.14891,14.61);(347.14891,14.61);(357.13326,17.09);(357.13326,17.09);(357.13326,17.09);(357.13326,17.09);(357.13326,17.09);(357.13326,17.09);(357.13326,17.09);(357.13326,17.09);(375.14383,21.18);(375.14383,21.18);(375.14383,21.18);(375.14383,21.18);(375.14383,21.18);(375.14383,21.18);(375.14383,21.18);(375.14383,21.18);(375.14383,21.18);(375.14383,21.18);(375.14383,21.18);(375.14383,21.18);(375.14383,21.18);(375.14383,21.18);(375.14383,21.18);(375.14383,21.18);(375.14383,21.18)
Predicted LC-MS/MS	Not Available	Positive	high	View Spectrum	(53.03858,30.89);(65.03858,83.6);(67.05423,34.36);(69.03349,16.16);(81.03349,14.85);(81.03349,14.85);(83.04914,16.01);(83.04914,16.01);(95.04914,14.14);(95.04914,14.14);(99.04406,13.28);(99.04406,13.28);(99.04406,13.28);(105.03349,14.43);(109.06479,63.6);(125.05971,18.81);(125.05971,18.81);(125.05971,18.81);(135.04406,22.82);(135.04406,22.82);(135.04406,22.82);(137.05971,100.0);(137.05971,100.0);(137.05971,100.0);(137.05971,100.0);(137.05971,100.0);(163.07536,15.28);(165.09101,20.87);(165.09101,20.87);(165.09101,20.87);(177.09101,12.76);(269.08084,13.82);(273.11214,33.05);(285.07575,19.63);(285.07575,19.63);(289.10705,22.26);(289.10705,22.26);(289.10705,22.26);(299.0914,15.98);(299.0914,15.98);(299.0914,15.98);(301.10705,19.25);(301.10705,19.25);(301.10705,19.25);(303.1227,33.97);(303.1227,33.97);(303.1227,33.97);(311.12779,15.05);(313.14344,14.47);(315.1227,13.03);(315.1227,13.03);(347.14891,18.88);(347.14891,18.88);(347.14891,18.88);(347.14891,18.88);(347.14891,18.88);(347.14891,18.88);(357.13326,12.8);(357.13326,12.8);(357.13326,12.8);(357.13326,12.8);(357.13326,12.8);(357.13326,12.8);(357.13326,12.8);(357.13326,12.8);(359.11253,13.58);(359.11253,13.58);(359.11253,13.58);(373.12818,11.16)
Predicted LC-MS/MS	Not Available	Negative	low	View Spectrum	(355.11871,2.96);(355.11871,2.96);(355.11871,2.96);(355.11871,2.96);(357.09798,3.84);(357.09798,3.84);(357.09798,3.84);(357.09798,3.84);(357.09798,3.84);(357.09798,3.84);(357.09798,3.84);(357.09798,3.84);(357.09798,3.84);(357.09798,3.84);(357.09798,3.84);(357.09798,3.84);(357.09798,3.84);(357.09798,3.84);(357.09798,3.84);(373.12928,100.0);(373.12928,100.0);(373.12928,100.0);(373.12928,100.0);(373.12928,100.0);(373.12928,100.0);(373.12928,100.0);(373.12928,100.0);(373.12928,100.0);(373.12928,100.0);(373.12928,100.0);(373.12928,100.0);(373.12928,100.0);(373.12928,100.0);(373.12928,100.0);(373.12928,100.0);(373.12928,100.0);(373.12928,100.0)
Predicted LC-MS/MS	Not Available	Negative	medium	View Spectrum	(107.01385,30.64);(121.0295,16.98);(121.0295,16.98);(123.04515,15.78);(123.04515,15.78);(123.04515,15.78);(123.04515,15.78);(123.04515,15.78);(135.04515,40.48);(135.04515,40.48);(135.04515,40.48);(135.04515,40.48);(137.02442,21.48);(151.04007,11.22);(151.04007,11.22);(151.04007,11.22);(205.05063,58.29);(205.05063,58.29);(219.0299,10.2);(219.06628,18.81);(219.06628,18.81);(219.06628,18.81);(219.06628,18.81);(221.04555,27.66);(223.0612,11.21);(223.0612,11.21);(223.0612,11.21);(231.06628,11.14);(231.06628,11.14);(231.06628,11.14);(233.04555,14.99);(233.04555,14.99);(233.04555,14.99);(233.08193,16.09);(233.08193,16.09);(233.08193,16.09);(233.08193,16.09);(233.08193,16.09);(235.0612,100.0);(235.0612,100.0);(235.0612,100.0);(235.0612,100.0);(243.0299,15.2);(249.07685,20.89);(249.07685,20.89);(249.07685,20.89);(249.07685,20.89);(249.07685,20.89);(251.0925,26.34);(251.0925,26.34);(251.0925,26.34);(251.0925,26.34);(251.0925,26.34);(251.0925,26.34);(251.0925,26.34);(251.0925,26.34);(251.0925,26.34);(251.0925,26.34);(311.0925,12.57);(313.10815,16.72);(313.10815,16.72);(313.10815,16.72);(315.1238,20.67);(329.10306,19.22);(329.10306,19.22);(329.10306,19.22);(329.10306,19.22);(329.10306,19.22);(329.10306,19.22);(329.10306,19.22);(329.10306,19.22);(329.10306,19.22);(339.08741,39.87);(339.08741,39.87);(339.08741,39.87);(339.08741,39.87);(339.08741,39.87);(339.08741,39.87);(341.06668,43.02);(341.10306,13.87);(341.10306,13.87);(341.10306,13.87);(341.10306,13.87);(355.08233,19.54);(355.08233,19.54);(355.11871,22.39);(355.11871,22.39);(355.11871,22.39);(355.11871,22.39);(357.09798,55.28);(357.09798,55.28);(357.09798,55.28);(357.09798,55.28);(357.09798,55.28);(357.09798,55.28);(357.09798,55.28);(357.09798,55.28);(357.09798,55.28);(357.09798,55.28);(357.09798,55.28);(357.09798,55.28);(357.09798,55.28);(357.09798,55.28);(357.09798,55.28);(371.11363,48.34);(371.11363,48.34);(371.11363,48.34);(371.11363,48.34);(371.11363,48.34);(371.11363,48.34);(371.11363,48.34);(371.11363,48.34);(371.11363,48.34);(373.12928,63.69);(373.12928,63.69);(373.12928,63.69);(373.12928,63.69);(373.12928,63.69);(373.12928,63.69);(373.12928,63.69);(373.12928,63.69);(373.12928,63.69);(373.12928,63.69);(373.12928,63.69);(373.12928,63.69);(373.12928,63.69);(373.12928,63.69);(373.12928,63.69);(373.12928,63.69);(373.12928,63.69);(373.12928,63.69)
Predicted LC-MS/MS	Not Available	Negative	high	View Spectrum	(105.03459,19.58);(107.01385,22.62);(109.0295,18.71);(113.02442,10.23);(115.04007,8.24);(121.0295,42.59);(121.0295,42.59);(123.04515,28.57);(123.04515,28.57);(123.04515,28.57);(123.04515,28.57);(123.04515,28.57);(135.04515,46.56);(135.04515,46.56);(135.04515,46.56);(135.04515,46.56);(137.02442,33.99);(137.0608,10.09);(137.0608,10.09);(205.05063,9.56);(205.05063,9.56);(207.06628,8.06);(207.06628,8.06);(219.06628,9.38);(219.06628,9.38);(219.06628,9.38);(219.06628,9.38);(233.04555,10.47);(233.04555,10.47);(233.04555,10.47);(235.0612,20.79);(235.0612,20.79);(235.0612,20.79);(235.0612,20.79);(243.0299,9.12);(275.0925,15.05);(287.0925,11.61);(287.0925,11.61);(287.0925,11.61);(287.0925,11.61);(287.0925,11.61);(297.07685,25.3);(297.07685,25.3);(297.07685,25.3);(299.0925,11.18);(299.0925,11.18);(299.0925,11.18);(301.10815,18.57);(301.10815,18.57);(301.10815,18.57);(301.10815,18.57);(301.10815,18.57);(317.10306,14.53);(317.10306,14.53);(317.10306,14.53);(317.10306,14.53);(327.08741,11.68);(327.08741,11.68);(327.08741,11.68);(327.08741,11.68);(329.10306,21.18);(329.10306,21.18);(329.10306,21.18);(329.10306,21.18);(329.10306,21.18);(329.10306,21.18);(329.10306,21.18);(329.10306,21.18);(329.10306,21.18);(339.08741,17.94);(339.08741,17.94);(339.08741,17.94);(339.08741,17.94);(339.08741,17.94);(339.08741,17.94);(341.06668,12.25);(343.11871,10.12);(343.11871,10.12);(343.11871,10.12);(343.11871,10.12);(343.11871,10.12);(345.13436,9.18);(345.13436,9.18);(345.13436,9.18);(345.13436,9.18);(345.13436,9.18);(345.13436,9.18);(355.11871,12.27);(355.11871,12.27);(355.11871,12.27);(355.11871,12.27);(371.11363,100.0);(371.11363,100.0);(371.11363,100.0);(371.11363,100.0);(371.11363,100.0);(371.11363,100.0);(371.11363,100.0);(371.11363,100.0);(371.11363,100.0)

Food Sources

No food source information available

Role as Biomarker of intake

No roles as Biomarker of intake found

Metabolism

	Food Phytochemical		Metabolite	Species	Biofluids	Origin	TMax	CMax	Urinary Excretion	Formula	Monoisotopic mass
	7-Hydroxymatairesinol		Enterolactone	Not Available	Not Available	Not Available	Not Available	Not Available	Not Available	C₁₈H₁₈O₄	298.12050906	Detailed Intervention Studies
	7-Hydroxymatairesinol		7-Hydroxymatairesinol	Not Available	Not Available	Not Available	Not Available	Not Available	Not Available	C₂₀H₂₂O₇	374.136553048	Detailed Intervention Studies

Inter-Individual Variations in Metabolism

	Food Phytochemical		Metabolite	Effect	Value

Back

Showing entry for 7-Hydroxymatairesinol

Identification

Structure for 7-Hydroxymatairesinol

Calculated Properties

External Links

Taxonomy as Food Phytochemical

Classyfire Taxonomy

Spectra from Phytohub

Food Sources

Role as Biomarker of intake

Metabolism

Inter-Individual Variations in Metabolism