4'-Hydroxyphenylvaleric acid
Showing entry for 4'-Hydroxyphenylvaleric acid
Identification
- PhytoHub ID
- PHUB001835
- Name
- 4'-Hydroxyphenylvaleric acid
- Systematic Name
- Not Available
- Synonyms
- Not Available
- CAS Number
- Not Available
- Average Mass
- 194.23
- Monoisotopic Mass
- 194.094294311
- Chemical Formula
- C11H14O3
- IUPAC Name
- 5-(4-hydroxyphenyl)pentanoic acid
- InChI Key
- YSSJQFONKASLKM-UHFFFAOYSA-N
- InChI Identifier
InChI=1S/C11H14O3/c12-10-7-5-9(6-8-10)3-1-2-4-11(13)14/h5-8,12H,1-4H2,(H,13,14)
- SMILES
OC(=O)CCCCC1=CC=C(O)C=C1
- Structure
Structure for 4'-Hydroxyphenylvaleric acid
Calculated Properties
- Solubility (ALOGPS)
- 4.33e-01 g/l
- LogS (ALOGPS)
- -2.65
- LogP (ALOGPS)
- 2.00
- Hydrogen Acceptors
- 3
- Hydrogen Donors
- 2
- Rotatable Bond Count
- 5
- Polar Surface Area
- 57.53
- Refractivity
- 53.1495
- Polarizability
- 21.113520347736145
- Formal Charge
- 0
- Physiological Charge
- -1
- pKa (strongest basic)
- -5.4407907499955925
- pKa (strongest acidic)
- 4.389895902988304
- Number of Rings
- 1
- Rule of Five
- Yes
- Bioavailability
- Yes
- Ghose Filter
- Yes
- Veber's Rule
- No
- MDDR-like Rule
- No
External Links
No external links
Taxonomy as Metabolite
- Family
- (Poly)phenol metabolites
- Class
- Flavonoid metabolites
- Sub-class
- Phenylvalerolactones and phenylvaleric acids
Classyfire Taxonomy
- Kingdom Name
- Organic compounds
- Class
- Fatty Acyls
- Super-class
- Lipids and lipid-like molecules
- Sub-class
- Fatty acids and conjugates
- Direct Parent Name
- Medium-chain fatty acids
- Alternative Parent Names
- ["1-hydroxy-2-unsubstituted benzenoids", "Benzene and substituted derivatives", "Carbonyl compounds", "Carboxylic acids", "Hydrocarbon derivatives", "Hydroxy fatty acids", "Monocarboxylic acids and derivatives", "Organic oxides"]
- External Descriptor Annotations
- Not Available
- Substituent Names
- ["1-hydroxy-2-unsubstituted benzenoid", "Aromatic homomonocyclic compound", "Benzenoid", "Carbonyl group", "Carboxylic acid", "Carboxylic acid derivative", "Hydrocarbon derivative", "Hydroxy fatty acid", "Medium-chain fatty acid", "Monocarboxylic acid or derivatives", "Monocyclic benzene moiety", "Organic oxide", "Organic oxygen compound", "Organooxygen compound", "Phenol"]
Spectra from Phytohub
| Spectrum Type | Instrument Type | Ion Mode | Collision Energy Level | View | Peaks | |
|---|---|---|---|---|---|---|
| Predicted GC-MS | GC-MS | Positive | Not Available | View Spectrum | (59.03115062,0.8727194122);(71.03115062,0.8408072709);(73.04679982,10.96663053);(74.04796012,0.9383733);(75.02606472,3.603286548);(89.04171392,4.108049003);(90.04953852,1.397216081);(91.05736312,1.353657336);(117.036628,2.092506066);(143.0522772,1.147398357);(144.0601018,0.8693954212);(145.0679264,0.9550356805);(157.0679264,0.8673519081);(159.0835756,1.051283374);(163.0573631,1.102908532);(179.0886615,7.08144103);(180.0908978,1.169844792);(191.0886615,1.944419713);(193.1043107,1.573654615);(205.1043107,2.109259135);(206.1121353,0.8485081349);(207.1199599,2.916517172);(220.1277845,0.8563559137);(221.1356091,3.308520002);(237.1305232,1.560931043);(249.1305232,2.546325737);(265.1254373,2.070302635);(266.1332619,2.141843);(267.1410865,1.198487947);(323.1493119,3.645640646);(324.151369,1.041000118) | |
| Predicted GC-MS | GC-MS | Positive | Not Available | View Spectrum | (25.00727602,1.170262804);(27.02292522,2.684903636);(41.03857442,1.006730766);(43.98927962,1.014025924);(44.99710422,3.747721158);(58.00492882,1.044924174);(59.01275342,1.218313262);(60.02057802,1.001986884);(71.01275342,1.490934806);(72.02057802,1.303674775);(73.02840262,2.080190563);(87.04405182,1.419480624);(94.04131312,0.9766588772);(105.0334885,6.019427653);(106.0413131,1.870294788);(107.0491377,12.43287046);(108.0525356,0.9919252094);(108.0569623,1.16771472);(119.0491377,4.103644387);(120.0569623,2.206957088);(121.0647869,5.157504559);(133.0647869,3.449273056);(134.0726115,1.274105768);(135.0804361,2.224049947);(147.0804361,1.366424342);(148.0882607,1.421928384);(149.0960853,1.561685767);(150.1039099,1.19230733);(176.0831748,1.749177524);(177.0909994,1.015822647);(194.0937381,1.79818332) | |
| Predicted GC-MS | GC-MS | Ei | Not Available | View Spectrum | (25.00727602,1.170262804);(27.02292522,2.684903636);(41.03857442,1.006730766);(43.98927962,1.014025924);(44.99710422,3.747721158);(58.00492882,1.044924174);(59.01275342,1.218313262);(60.02057802,1.001986884);(71.01275342,1.490934806);(72.02057802,1.303674775);(73.02840262,2.080190563);(87.04405182,1.419480624);(94.04131312,0.9766588772);(105.0334885,6.019427653);(106.0413131,1.870294788);(107.0491377,12.43287046);(108.0525356,0.9919252094);(108.0569623,1.16771472);(119.0491377,4.103644387);(120.0569623,2.206957088);(121.0647869,5.157504559);(133.0647869,3.449273056);(134.0726115,1.274105768);(135.0804361,2.224049947);(147.0804361,1.366424342);(148.0882607,1.421928384);(149.0960853,1.561685767);(150.1039099,1.19230733);(176.0831748,1.749177524);(177.0909994,1.015822647);(194.0937381,1.79818332) | |
| Predicted LC-MS/MS | Not Available | Positive | low | View Spectrum | (107.0491413,1.360809871);(135.0804414,2.417226911);(149.0960915,6.417958717);(159.0804414,7.87721293);(177.0910061,46.8316543);(195.1015708,20.2637251) | |
| Predicted LC-MS/MS | Not Available | Positive | med | View Spectrum | (39.02292652,2.109225578);(41.03857658,2.607423867);(53.00219107,0.7587977363);(55.01784114,0.7404134663);(55.05422664,1.301491007);(67.01784114,1.263417763);(69.0334912,1.493771654);(73.02840582,0.8551192223);(81.0334912,0.7604075918);(83.04914126,1.217108467);(87.04405588,1.819805367);(95.04914126,0.8675495253);(101.0597059,1.216398007);(105.0334912,2.401564558);(107.0491413,5.648466575);(109.0647913,1.185795189);(119.0491413,1.187384975);(121.0647913,1.644870282);(133.0647913,1.963103746);(135.0804414,6.661665155);(147.0804414,1.146656057);(149.0960915,14.11994724);(151.1117415,1.31256999);(159.0804414,4.607298502);(177.0910061,14.82301807);(195.1015708,6.89800737) | |
| Predicted LC-MS/MS | Not Available | Positive | high | View Spectrum | (25.00727645,1.083374953);(27.02292652,2.794847048);(39.02292652,4.881564118);(41.03857658,10.2365896);(43.05422664,2.257849963);(55.05422664,2.636366243);(59.01275576,1.314374737);(65.00219107,1.230653952);(65.03857658,1.354662838);(68.99710569,1.468128135);(75.02292652,1.114727838);(77.03857658,1.828013765);(79.05422664,2.935801737);(91.05422664,1.418458256);(93.06987671,1.628109678);(103.0542266,1.335540863);(105.0334912,3.067814466);(105.0698767,2.457410957);(107.0491413,5.759460455);(107.0855268,1.679832654);(115.0542266,1.276352051);(117.0698767,1.197731716);(119.0491413,1.438485069);(119.0855268,2.89714993);(121.0647913,1.35175284);(121.1011768,1.214325745);(131.0491413,1.061993815);(131.0855268,1.155430228);(133.0647913,2.265241088);(135.0804414,2.059732134);(149.0960915,2.110143241) | |
| Predicted LC-MS/MS | Not Available | Negative | low | View Spectrum | (59.01385292,1.353410861);(147.0815386,0.8877648748);(149.0971886,11.54127001);(165.0921032,0.5282677454);(175.0764532,16.50045527);(193.0870179,66.10339832) | |
| Predicted LC-MS/MS | Not Available | Negative | med | View Spectrum | (59.01385292,4.814690708);(147.0815386,3.28865045);(149.0971886,17.88923177);(165.0921032,1.784488942);(175.0764532,25.43290458);(193.0870179,31.97074476) | |
| Predicted LC-MS/MS | Not Available | Negative | high | View Spectrum | (41.00328823,13.86562459);(43.0189383,3.099084323);(44.99820285,4.232672484);(59.01385292,21.16675258);(61.02950298,1.114361446);(93.03458836,3.540981984);(105.0345884,1.625555277);(107.0502384,3.105660027);(119.0502384,1.1031767);(119.0866239,1.571294599);(121.0658885,1.261580664);(131.0866239,1.666598331);(133.0658885,2.484296584);(145.0658885,2.270867);(147.0815386,4.958052153);(149.0971886,4.942381654);(157.0658885,1.34458322);(175.0764532,5.460730478);(193.0870179,1.429104879) | |
| Predicted LC-MS/MS | Not Available | Negative | low | View Spectrum | (193.08702,100.0);(193.08702,100.0);(193.08702,100.0);(193.08702,100.0) | |
| Predicted LC-MS/MS | Not Available | Negative | medium | View Spectrum | (59.01385,12.12);(93.03459,17.94);(93.03459,17.94);(93.03459,17.94);(93.03459,17.94);(105.03459,15.1);(105.03459,15.1);(107.05024,18.06);(107.05024,18.06);(107.05024,18.06);(119.05024,30.48);(119.05024,30.48);(119.05024,30.48);(119.05024,30.48);(121.06589,51.44);(121.06589,51.44);(121.06589,51.44);(121.06589,51.44);(133.06589,9.76);(133.06589,9.76);(147.08154,8.44);(149.09719,28.44);(149.09719,28.44);(175.07645,42.74);(175.07645,42.74);(193.08702,100.0);(193.08702,100.0);(193.08702,100.0);(193.08702,100.0) | |
| Predicted LC-MS/MS | Not Available | Negative | high | View Spectrum | (41.00329,27.5);(59.01385,10.01);(63.02402,8.44);(67.01894,13.73);(91.05532,5.94);(93.03459,100.0);(93.03459,100.0);(93.03459,100.0);(93.03459,100.0);(101.03967,5.94);(105.03459,12.72);(105.03459,12.72);(107.05024,16.18);(107.05024,16.18);(107.05024,16.18);(117.03459,28.48);(117.03459,28.48);(117.03459,28.48);(119.05024,48.27);(119.05024,48.27);(119.05024,48.27);(119.05024,48.27);(121.06589,10.63);(121.06589,10.63);(121.06589,10.63);(121.06589,10.63);(123.04515,5.78);(131.05024,5.85);(131.05024,5.85);(131.05024,5.85) | |
| Predicted LC-MS/MS | Not Available | Positive | low | View Spectrum | (79.05423,7.72);(79.05423,7.72);(105.03349,12.25);(105.03349,12.25);(105.03349,12.25);(107.04914,56.95);(107.04914,56.95);(107.04914,56.95);(107.04914,56.95);(121.06479,6.21);(121.06479,6.21);(121.06479,6.21);(121.06479,6.21);(121.06479,6.21);(123.08044,12.06);(123.08044,12.06);(123.08044,12.06);(123.08044,12.06);(133.06479,7.54);(133.06479,7.54);(133.06479,7.54);(133.06479,7.54);(135.08044,40.37);(135.08044,40.37);(135.08044,40.37);(135.08044,40.37);(149.09609,10.32);(149.09609,10.32);(149.09609,10.32);(149.09609,10.32);(177.09101,29.26);(177.09101,29.26);(177.09101,29.26);(177.09101,29.26);(177.09101,29.26);(195.10157,100.0);(195.10157,100.0);(195.10157,100.0);(195.10157,100.0) | |
| Predicted LC-MS/MS | Not Available | Positive | medium | View Spectrum | (41.03858,10.93);(55.05423,28.81);(57.03349,10.17);(71.04914,13.5);(77.03858,17.11);(77.03858,17.11);(79.05423,18.64);(79.05423,18.64);(83.04914,13.73);(83.04914,13.73);(91.05423,41.04);(91.05423,41.04);(91.05423,41.04);(91.05423,41.04);(93.03349,7.71);(93.03349,7.71);(93.06988,23.7);(93.06988,23.7);(93.06988,23.7);(95.04914,26.11);(95.04914,26.11);(95.04914,26.11);(95.04914,26.11);(103.05423,9.28);(105.03349,16.73);(105.03349,16.73);(105.03349,16.73);(107.04914,100.0);(107.04914,100.0);(107.04914,100.0);(107.04914,100.0);(107.08553,14.21);(109.06479,12.91);(109.06479,12.91);(109.06479,12.91);(109.06479,12.91);(119.04914,17.5);(119.04914,17.5);(119.04914,17.5);(119.04914,17.5);(121.06479,61.87);(121.06479,61.87);(121.06479,61.87);(121.06479,61.87);(121.06479,61.87);(123.08044,10.28);(123.08044,10.28);(123.08044,10.28);(123.08044,10.28);(131.04914,27.96);(133.06479,37.18);(133.06479,37.18);(133.06479,37.18);(133.06479,37.18);(135.08044,27.77);(135.08044,27.77);(135.08044,27.77);(135.08044,27.77);(147.08044,17.13);(147.08044,17.13);(147.08044,17.13);(147.08044,17.13);(149.09609,52.37);(149.09609,52.37);(149.09609,52.37);(149.09609,52.37);(159.08044,38.27);(159.08044,38.27);(177.09101,48.76);(177.09101,48.76);(177.09101,48.76);(177.09101,48.76);(177.09101,48.76);(195.10157,13.17);(195.10157,13.17);(195.10157,13.17);(195.10157,13.17) | |
| Predicted LC-MS/MS | Not Available | Positive | high | View Spectrum | (41.03858,19.13);(51.02293,7.79);(53.03858,6.37);(55.05423,16.85);(65.03858,25.98);(65.03858,25.98);(67.05423,6.23);(77.03858,61.96);(77.03858,61.96);(79.05423,67.41);(79.05423,67.41);(81.06988,6.66);(81.06988,6.66);(89.03858,9.88);(89.03858,9.88);(91.05423,100.0);(91.05423,100.0);(91.05423,100.0);(91.05423,100.0);(93.06988,10.72);(93.06988,10.72);(93.06988,10.72);(95.04914,9.05);(95.04914,9.05);(95.04914,9.05);(95.04914,9.05);(105.03349,9.17);(105.03349,9.17);(105.03349,9.17);(105.06988,11.02);(107.04914,45.06);(107.04914,45.06);(107.04914,45.06);(107.04914,45.06);(107.08553,7.08);(115.05423,12.48);(117.06988,8.74);(117.06988,8.74);(119.08553,8.49);(121.06479,12.26);(121.06479,12.26);(121.06479,12.26);(121.06479,12.26);(121.06479,12.26);(129.06988,10.99);(131.08553,5.81);(149.09609,6.93);(149.09609,6.93);(149.09609,6.93);(149.09609,6.93);(151.07536,5.78);(153.09101,5.78) |
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
No metabolism information available
Inter-Individual Variations in Metabolism
No data on inter-individual variations available