Identification

PhytoHub ID
PHUB002288
Name
hydroxyphenylacetic acid-3′-sulfate
Systematic Name
hydroxyphenylacetic acid-3′-sulfate
Synonyms
Not Available
CAS Number
Not Available
Average Mass
232.21
Monoisotopic Mass
232.004159152
Chemical Formula
C8H8O6S
IUPAC Name
2-[4-(sulfooxy)phenyl]acetic acid
InChI Key
IIODELUADFSHIZ-UHFFFAOYSA-N
InChI Identifier
InChI=1S/C8H8O6S/c9-8(10)5-6-1-3-7(4-2-6)14-15(11,12)13/h1-4H,5H2,(H,9,10)(H,11,12,13)
SMILES
OC(=O)CC1=CC=C(OS(O)(=O)=O)C=C1
Structure

Calculated Properties

Solubility (ALOGPS)
2.11e+00 g/l
LogS (ALOGPS)
-2.04
LogP (ALOGPS)
-0.87
Hydrogen Acceptors
5
Hydrogen Donors
2
Rotatable Bond Count
4
Polar Surface Area
100.9
Refractivity
49.33830000000001
Polarizability
20.01849551570762
Formal Charge
0
Physiological Charge
-2
pKa (strongest basic)
Not Available
pKa (strongest acidic)
-2.20249925048582
Number of Rings
1
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
Phenolic acid metabolites
Sub-class
Phenylacetic acids

Taxonomy of its Food Phytochemical Precursor(s)

Food PhytochemicalFamilyClassSub-class
Orange flavanonesPolyphenolsFlavonoidsFlavanonesShow Food Phytochemical

Classyfire Taxonomy

Kingdom Name
Organic compounds
Class
Organic sulfuric acids and derivatives
Super-class
Organic acids and derivatives
Sub-class
Arylsulfates
Direct Parent Name
Phenylsulfates
Alternative Parent Names
["Carbonyl compounds", "Carboxylic acids", "Hydrocarbon derivatives", "Monocarboxylic acids and derivatives", "Organic oxides", "Phenoxy compounds", "Sulfuric acid monoesters"]
External Descriptor Annotations
Not Available
Substituent Names
["Aromatic homomonocyclic compound", "Benzenoid", "Carbonyl group", "Carboxylic acid", "Carboxylic acid derivative", "Hydrocarbon derivative", "Monocarboxylic acid or derivatives", "Monocyclic benzene moiety", "Organic oxide", "Organic oxygen compound", "Organooxygen compound", "Phenoxy compound", "Phenylsulfate", "Sulfate-ester", "Sulfuric acid ester", "Sulfuric acid monoester"]

Spectra from Phytohub

Spectrum TypeInstrument TypeIon ModeCollision Energy LevelViewPeaks
Predicted GC-MSGC-MSPositiveNot AvailableView Spectrum(57.01550142,0.9319349688);(59.03115062,0.8404683158);(71.03115062,0.9854835837);(73.01041552,0.8607523871);(73.04679982,7.994158743);(74.04796012,0.6840300765);(74.05462442,0.7958793362);(75.02606472,2.557796296);(75.06244902,0.7716601718);(89.04171392,3.659496172);(90.04953852,1.479401035);(91.05736312,1.277381395);(105.0334885,2.165449276);(107.0491377,2.150513739);(117.036628,2.046569301);(172.9903008,1.003410967);(185.9981254,1.832568486);(187.00595,21.8009018);(188.0090017,1.935925821);(188.0137746,3.139884743);(189.0036185,1.219603625);(189.0215992,1.872280288);(195.0835756,1.076980615);(209.0628405,1.141682024);(215.0008641,3.512621621);(223.0784897,1.250795025);(224.0863143,0.7615546755);(232.0036028,0.8143657566);(287.0403879,0.6612024727);(289.0196528,1.723523264);(304.0431266,0.6731118984)
Predicted GC-MSGC-MSPositiveNot AvailableView Spectrum(23.99945142,0.6071370858);(25.00727602,0.6548898986);(27.02292522,0.8239091721);(44.99710422,2.175937649);(80.96408832,1.016627784);(91.05422362,0.7222732741);(105.0334885,2.291264534);(107.0491377,3.974016921);(108.0569623,1.266851538);(121.0284026,1.079051654);(123.0440518,2.690721417);(134.0362272,0.6477388357);(135.0440518,0.7788848498);(148.0154921,0.8329066521);(149.0233167,0.9872330117);(150.0311413,0.6694160399);(151.0389659,2.153532161);(152.0467905,2.120081829);(158.9746516,0.9168195353);(171.9824762,1.065330248);(172.9903008,1.770217218);(185.9981254,6.376422681);(187.00595,20.47427774);(188.0090017,1.818121255);(188.0137746,3.240288425);(189.0036185,1.145388553);(213.9930395,1.628891835);(215.0008641,1.774353598);(229.9879536,0.782620163);(230.9957782,0.5967291195);(232.0036028,2.14099718)
Predicted GC-MSGC-MSEiNot AvailableView Spectrum(23.99945142,0.6071370858);(25.00727602,0.6548898986);(27.02292522,0.8239091721);(44.99710422,2.175937649);(80.96408832,1.016627784);(91.05422362,0.7222732741);(105.0334885,2.291264534);(107.0491377,3.974016921);(108.0569623,1.266851538);(121.0284026,1.079051654);(123.0440518,2.690721417);(134.0362272,0.6477388357);(135.0440518,0.7788848498);(148.0154921,0.8329066521);(149.0233167,0.9872330117);(150.0311413,0.6694160399);(151.0389659,2.153532161);(152.0467905,2.120081829);(158.9746516,0.9168195353);(171.9824762,1.065330248);(172.9903008,1.770217218);(185.9981254,6.376422681);(187.00595,20.47427774);(188.0090017,1.818121255);(188.0137746,3.240288425);(189.0036185,1.145388553);(213.9930395,1.628891835);(215.0008641,1.774353598);(229.9879536,0.782620163);(230.9957782,0.5967291195);(232.0036028,2.14099718)
Predicted GC-MSGC-MSEiNot AvailableView Spectrum(23.99945142,0.6071370858);(25.00727602,0.6548898986);(27.02292522,0.8239091721);(44.99710422,2.175937649);(80.96408832,1.016627784);(91.05422362,0.7222732741);(105.0334885,2.291264534);(107.0491377,3.974016921);(108.0569623,1.266851538);(121.0284026,1.079051654);(123.0440518,2.690721417);(134.0362272,0.6477388357);(135.0440518,0.7788848498);(148.0154921,0.8329066521);(149.0233167,0.9872330117);(150.0311413,0.6694160399);(151.0389659,2.153532161);(152.0467905,2.120081829);(158.9746516,0.9168195353);(171.9824762,1.065330248);(172.9903008,1.770217218);(185.9981254,6.376422681);(187.00595,20.47427774);(188.0090017,1.818121255);(188.0137746,3.240288425);(189.0036185,1.145388553);(213.9930395,1.628891835);(215.0008641,1.774353598);(229.9879536,0.782620163);(230.9957782,0.5967291195);(232.0036028,2.14099718)
Predicted LC-MS/MSNot AvailablePositivelowView Spectrum(135.0440559,2.657853698);(172.9903061,5.03973112);(187.0059561,9.897869427);(196.9903061,8.475518887);(215.0008707,47.22997184);(233.0114354,17.53468641)
Predicted LC-MS/MSNot AvailablePositivemedView Spectrum(105.0334912,3.236195136);(107.0491413,12.52082943);(135.0440559,16.2116696);(153.0546206,4.642493244);(172.9903061,6.050563418);(187.0059561,13.89539376);(196.9903061,5.785096561);(215.0008707,14.56233733);(233.0114354,3.658220635)
Predicted LC-MS/MSNot AvailablePositivehighView Spectrum(49.00727645,1.671891368);(51.02292652,2.836173699);(63.02292652,13.84185895);(65.03857658,1.909353006);(75.02292652,6.244602926);(77.03857658,17.80102239);(79.05422664,2.727635544);(91.05422664,9.898855785);(103.0178411,1.831990609);(105.0334912,3.970447994);(117.0334912,2.207684843);(119.0127558,3.349013166);(119.0491413,2.360693429);(135.0440559,3.684282333);(172.9903061,3.232540207);(187.0059561,2.722285644)
Predicted LC-MS/MSNot AvailableNegativelowView Spectrum(107.0502384,0.9909265289);(133.029503,0.9354675568);(151.0400677,2.847175327);(187.0070533,27.8900268);(212.9863178,12.76910245);(230.9968825,49.39488072)
Predicted LC-MS/MSNot AvailableNegativemedView Spectrum(105.0345884,9.570147862);(107.0502384,8.06278648);(133.029503,11.07173031);(151.0400677,19.26153167);(187.0070533,11.91626011);(212.9863178,10.44550684);(230.9968825,12.20804498)
Predicted LC-MS/MSNot AvailableNegativehighView Spectrum(59.01385292,4.804034303);(80.96518847,11.64935419);(105.0345884,13.08927107);(107.0502384,12.01328098);(133.029503,29.68603655);(151.0400677,9.637179071)
Predicted LC-MS/MSNot AvailablePositivelowView Spectrum(215.00087,24.51);(215.00087,24.51);(215.00087,24.51);(215.00087,24.51);(215.00087,24.51);(233.01144,100.0);(233.01144,100.0);(233.01144,100.0);(233.01144,100.0)
Predicted LC-MS/MSNot AvailablePositivemediumView Spectrum(91.05423,24.4);(107.04914,32.99);(135.04406,36.47);(135.04406,36.47);(135.04406,36.47);(171.01104,25.07);(187.00596,22.16);(187.00596,22.16);(196.99031,15.64);(215.00087,100.0);(215.00087,100.0);(215.00087,100.0);(215.00087,100.0);(215.00087,100.0);(233.01144,56.5);(233.01144,56.5);(233.01144,56.5);(233.01144,56.5)
Predicted LC-MS/MSNot AvailablePositivehighView Spectrum(51.02293,29.85);(65.03858,26.94);(65.03858,26.94);(75.02293,10.98);(77.03858,31.31);(91.05423,91.46);(93.06988,11.13);(105.03349,40.0);(105.03349,40.0);(107.04914,100.0);(117.03349,15.79);(119.04914,26.94);(135.04406,14.4);(135.04406,14.4);(135.04406,14.4);(171.01104,23.01)
Predicted LC-MS/MSNot AvailableNegativelowView Spectrum(187.00705,45.24);(187.00705,45.24);(187.00705,45.24);(230.99688,100.0);(230.99688,100.0);(230.99688,100.0)
Predicted LC-MS/MSNot AvailableNegativemediumView Spectrum(187.00705,100.0);(187.00705,100.0);(187.00705,100.0);(230.99688,26.63);(230.99688,26.63);(230.99688,26.63)
Predicted LC-MS/MSNot AvailableNegativehighView Spectrum(59.01385,19.93);(65.00329,24.07);(65.03967,36.46);(75.02402,92.9);(77.03967,100.0);(80.96519,48.44);(83.01385,14.59);(92.9982,25.81);(96.9601,38.52);(103.01894,13.82);(119.01385,11.93);(120.9601,61.61);(121.0295,33.79);(133.0295,11.87);(134.97575,12.35);(158.97575,13.54);(158.97575,13.54);(187.00705,13.33);(187.00705,13.33);(187.00705,13.33);(212.98632,11.84);(212.98632,11.84);(212.98632,11.84)

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
Orange flavanones hydroxyphenylacetic acid-3′-sulfateNot AvailableNot AvailableNot AvailableNot AvailableNot AvailableNot AvailableC8H8O6S232.004159152 Detailed Intervention Studies

Inter-Individual Variations in Metabolism

Food PhytochemicalMetaboliteEffectValue
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