Guaiacol sulfate
Showing entry for Guaiacol sulfate
Identification
- PhytoHub ID
- PHUB002488
- Name
- Guaiacol sulfate
- Systematic Name
- 2-Methoxybenzene-1-sulfate
- Synonyms
- Not Available
- CAS Number
- Not Available
- Average Mass
- 204.2
- Monoisotopic Mass
- 204.009244532
- Chemical Formula
- C7H8O5S
- IUPAC Name
- (2-methoxyphenyl)oxidanesulfonic acid
- InChI Key
- ASHYAXWNZMCQPW-UHFFFAOYSA-N
- InChI Identifier
InChI=1S/C7H16O4S/c1-11-6-4-2-3-5-7(6)12(8,9)10/h6-10H,2-5H2,1H3
- SMILES
COC1=C(OS(O)(=O)=O)C=CC=C1
- Structure
Calculated Properties
- Solubility (ALOGPS)
- Not Available
- LogS (ALOGPS)
- Not Available
- LogP (ALOGPS)
- Not Available
- Hydrogen Acceptors
- 4
- Hydrogen Donors
- 1
- Rotatable Bond Count
- 3
- Polar Surface Area
- 72.83
- Refractivity
- 44.493900000000004
- Polarizability
- 17.912138338083178
- Formal Charge
- 0
- Physiological Charge
- -1
- pKa (strongest basic)
- -4.9176657354695115
- pKa (strongest acidic)
- -2.2794163475347817
- 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
- Phenolic acid metabolites
- Sub-class
- Benzoic and hippuric acids
Taxonomy of its Food Phytochemical Precursor(s)
Food Phytochemical | Family | Class | Sub-class | |
---|---|---|---|---|
Coffee Chlorogenic acids | Polyphenols | Phenolic acids | Hydroxycinnamic acids | Show Food Phytochemical |
Spectra from Phytohub
Spectrum Type | Instrument Type | Ion Mode | Collision Energy Level | View | Peaks | |
---|---|---|---|---|---|---|
Predicted GC-MS | GC-MS | Positive | Not Available | View Spectrum | (39.02292522,1.603592588);(49.00727602,1.251293284);(51.02292522,1.11834099);(53.03857442,2.325582766);(78.01001472,0.8820289292);(79.01783932,2.250706814);(80.02566392,1.284177531);(80.96408832,1.924303546);(81.03348852,1.055541351);(93.03348852,1.214134467);(94.04131312,2.149246997);(95.04913772,3.595872321);(106.0413131,0.8987646366);(108.0569623,1.034023512);(109.0284026,1.397150571);(122.0362272,2.24300727);(123.0440518,3.636418858);(124.0518764,6.309297906);(144.9590024,0.8525041384);(157.966827,0.8898137785);(158.9746516,1.824350275);(159.9824762,1.55413085);(160.9903008,4.679509903);(171.9824762,1.093395564);(172.9903008,1.172676326);(173.9981254,1.497789429);(187.00595,1.525776928);(187.9773903,1.318266313);(188.9852149,2.109948103);(203.0008641,1.447846863);(204.0086887,6.437809346) | |
Predicted GC-MS | GC-MS | Ei | Not Available | View Spectrum | (39.02292522,2.517067037);(49.00727602,1.379164861);(50.01510062,0.9434930982);(51.02292522,1.137845376);(52.03074982,0.9588123637);(53.03857442,2.485606418);(78.01001472,0.9205386723);(79.01783932,2.153888246);(80.02566392,1.28397473);(80.96408832,1.902691585);(81.03348852,0.9411453386);(93.03348852,1.192387602);(94.04131312,2.11750585);(95.04913772,3.522212047);(106.0413131,0.8886705607);(108.0569623,1.022410337);(109.0284026,1.371121983);(122.0362272,2.21737242);(123.0440518,3.527690157);(124.0518764,6.086847518);(158.9746516,1.810292036);(159.9824762,1.534988292);(160.9903008,4.641398766);(171.9824762,1.081115578);(172.9903008,1.159505932);(173.9981254,1.48032456);(187.00595,1.457365042);(187.9773903,1.302894761);(188.9852149,2.099907571);(203.0008641,1.431586014);(204.0086887,6.3190223) | |
LC-MS/MS | Not Available | Negative | Not Available | View Spectrum | (79.9562,8.75);(108.0206,100.0);(123.0442,14.76) | |
LC-MS/MS | Not Available | Negative | Not Available | View Spectrum | (79.9561,5.0);(108.0207,6.22);(123.0445,30.2);(203.001,100.0) | |
LC-MS/MS | LC-ESI-QTOF | Negative | low | View Spectrum | (79.9561,0.05002255);(108.0207,0.06220117);(123.0445,0.30202977);(187.9772,0.00507442);(203.001,1.0);(203.0772,0.01275147);(203.1182,0.00594046) | |
LC-MS/MS | LC-ESI-QTOF | Negative | medium | View Spectrum | (79.9562,0.08751109);(80.0259,0.00261757);(108.0206,1.0);(123.0442,0.14760426) | |
Predicted LC-MS/MS | Not Available | Positive | low | View Spectrum | (80.96409131,1.371722843);(95.04914126,2.317609688);(107.0491413,3.824394139);(172.9903061,1.367064549);(187.0059561,12.58132816);(205.0165208,70.42554607) | |
Predicted LC-MS/MS | Not Available | Positive | med | View Spectrum | (80.96409131,5.249399653);(107.0491413,11.70708196);(109.0284058,2.909882866);(123.0440559,3.389464813);(125.0597059,22.67247592);(187.0059561,20.84687793);(205.0165208,14.31203894) | |
Predicted LC-MS/MS | Not Available | Positive | high | View Spectrum | (15.02292652,1.184758987);(39.02292652,6.155690955);(49.00727645,10.84893629);(51.02292652,16.09816854);(53.03857658,9.663472344);(55.01784114,1.571022669);(55.05422664,2.885508839);(63.02292652,10.32059068);(65.03857658,7.305535498);(79.01784114,2.226946453);(80.96409131,2.754280138);(81.0334912,1.590380076);(95.04914126,2.178032334);(98.974656,2.156361513);(107.0491413,4.155557973) | |
Predicted LC-MS/MS | Not Available | Negative | low | View Spectrum | (80.96518847,1.144887763);(93.03458836,0.6397899661);(96.96010309,1.523586521);(107.0502384,0.5535101841);(123.045153,5.787370739);(203.0019679,87.82029206) | |
Predicted LC-MS/MS | Not Available | Negative | med | View Spectrum | (93.03458836,3.107272564);(96.96010309,3.101152955);(107.0138529,17.88467025);(107.0502384,2.203719848);(123.045153,34.99750056);(203.0019679,22.60827459) | |
Predicted LC-MS/MS | Not Available | Negative | high | View Spectrum | (63.02402368,2.925860183);(79.0189383,6.610771646);(80.96518847,15.97574248);(93.03458836,6.31640339);(96.96010309,2.786771029);(107.0138529,34.68103335);(123.045153,7.995402689);(158.9757532,3.306021386) | |
Predicted LC-MS/MS | Not Available | Positive | low | View Spectrum | (123.04406,28.24);(123.04406,28.24);(123.04406,28.24);(123.04406,28.24);(123.04406,28.24);(123.04406,28.24);(123.04406,28.24);(125.05971,89.87);(125.05971,89.87);(125.05971,89.87);(125.05971,89.87);(125.05971,89.87);(125.05971,89.87);(125.05971,89.87);(187.00596,16.88);(205.01652,100.0);(205.01652,100.0);(205.01652,100.0);(205.01652,100.0);(205.01652,100.0);(205.01652,100.0);(205.01652,100.0) | |
Predicted LC-MS/MS | Not Available | Positive | medium | View Spectrum | (55.05423,9.85);(80.96409,9.59);(81.03349,15.44);(81.03349,15.44);(81.03349,15.44);(93.03349,26.39);(95.04914,11.67);(95.04914,11.67);(97.06479,33.7);(97.06479,33.7);(98.97466,12.65);(109.02841,57.06);(109.02841,57.06);(123.04406,38.9);(123.04406,38.9);(123.04406,38.9);(123.04406,38.9);(123.04406,38.9);(123.04406,38.9);(123.04406,38.9);(125.05971,100.0);(125.05971,100.0);(125.05971,100.0);(125.05971,100.0);(125.05971,100.0);(125.05971,100.0);(125.05971,100.0);(205.01652,9.44);(205.01652,9.44);(205.01652,9.44);(205.01652,9.44);(205.01652,9.44);(205.01652,9.44);(205.01652,9.44) | |
Predicted LC-MS/MS | Not Available | Positive | high | View Spectrum | (39.02293,14.04);(41.03858,13.35);(51.02293,22.14);(53.03858,28.65);(63.02293,12.37);(65.03858,22.0);(81.03349,11.72);(81.03349,11.72);(81.03349,11.72);(95.04914,13.75);(95.04914,13.75);(107.04914,39.32);(107.04914,39.32);(107.04914,39.32);(107.04914,39.32);(109.02841,50.85);(109.02841,50.85);(123.04406,100.0);(123.04406,100.0);(123.04406,100.0);(123.04406,100.0);(123.04406,100.0);(123.04406,100.0);(123.04406,100.0) | |
Predicted LC-MS/MS | Not Available | Negative | low | View Spectrum | (203.00197,100.0);(203.00197,100.0);(203.00197,100.0);(203.00197,100.0);(203.00197,100.0);(203.00197,100.0);(203.00197,100.0) | |
Predicted LC-MS/MS | Not Available | Negative | medium | View Spectrum | (80.96519,28.43);(96.9601,100.0);(172.9914,33.3);(172.9914,33.3);(172.9914,33.3);(203.00197,27.57);(203.00197,27.57);(203.00197,27.57);(203.00197,27.57);(203.00197,27.57);(203.00197,27.57);(203.00197,27.57) | |
Predicted LC-MS/MS | Not Available | Negative | high | View Spectrum | (80.96519,26.92);(96.9601,100.0);(172.9914,7.47);(172.9914,7.47);(172.9914,7.47) |
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 Phytochemical | Metabolite | Species | Biofluids | Origin | TMax | CMax | Urinary Excretion | Formula | Monoisotopic mass | ||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Coffee Chlorogenic acids | Guaiacol sulfate | human | plasma | host-gut microbiota co-metabolite | <1h | 200-500 nmol/L | Not Available | C7H8O5S | 204.009244532 | Detailed Intervention Studies | Publications |
Inter-Individual Variations in Metabolism
Food Phytochemical | Metabolite | Effect | Value |
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