Record Information |
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Version | 5.0 |
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Status | Expected but not Quantified |
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Creation Date | 2012-09-12 00:07:07 UTC |
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Update Date | 2022-03-07 02:55:54 UTC |
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HMDB ID | HMDB0038773 |
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Secondary Accession Numbers | |
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Metabolite Identification |
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Common Name | Formononetin 7-(2-p-hydroxybenzoylglucoside) |
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Description | Formononetin 7-(2-p-hydroxybenzoylglucoside) belongs to the class of organic compounds known as isoflavonoid o-glycosides. These are o-glycosylated derivatives of isoflavonoids, which are natural products derived from 3-phenylchromen-4-one. Formononetin 7-(2-p-hydroxybenzoylglucoside) has been detected, but not quantified in, several different foods, such as herbal tea, green tea, herbs and spices, pulses, and red tea. This could make formononetin 7-(2-p-hydroxybenzoylglucoside) a potential biomarker for the consumption of these foods. Based on a literature review very few articles have been published on Formononetin 7-(2-p-hydroxybenzoylglucoside). |
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Structure | COC1=CC=C(C=C1)C1=COC2=C(C=CC(OC3OC(CO)C(O)C(O)C3OC(=O)C3=CC=C(O)C=C3)=C2)C1=O InChI=1S/C29H26O11/c1-36-18-8-4-15(5-9-18)21-14-37-22-12-19(10-11-20(22)24(21)32)38-29-27(26(34)25(33)23(13-30)39-29)40-28(35)16-2-6-17(31)7-3-16/h2-12,14,23,25-27,29-31,33-34H,13H2,1H3 |
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Synonyms | Value | Source |
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Formononetin 7-O-(2''-P-hydroxybenzoylglucoside) | HMDB | 4,5-Dihydroxy-6-(hydroxymethyl)-2-{[3-(4-methoxyphenyl)-4-oxo-4H-chromen-7-yl]oxy}oxan-3-yl 4-hydroxybenzoic acid | Generator |
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Chemical Formula | C29H26O11 |
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Average Molecular Weight | 550.5101 |
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Monoisotopic Molecular Weight | 550.147511674 |
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IUPAC Name | 4,5-dihydroxy-6-(hydroxymethyl)-2-{[3-(4-methoxyphenyl)-4-oxo-4H-chromen-7-yl]oxy}oxan-3-yl 4-hydroxybenzoate |
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Traditional Name | 4,5-dihydroxy-6-(hydroxymethyl)-2-{[3-(4-methoxyphenyl)-4-oxochromen-7-yl]oxy}oxan-3-yl 4-hydroxybenzoate |
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CAS Registry Number | 122130-27-2 |
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SMILES | COC1=CC=C(C=C1)C1=COC2=C(C=CC(OC3OC(CO)C(O)C(O)C3OC(=O)C3=CC=C(O)C=C3)=C2)C1=O |
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InChI Identifier | InChI=1S/C29H26O11/c1-36-18-8-4-15(5-9-18)21-14-37-22-12-19(10-11-20(22)24(21)32)38-29-27(26(34)25(33)23(13-30)39-29)40-28(35)16-2-6-17(31)7-3-16/h2-12,14,23,25-27,29-31,33-34H,13H2,1H3 |
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InChI Key | PDHVVKASGTXJHE-UHFFFAOYSA-N |
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Chemical Taxonomy |
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Description | Belongs to the class of organic compounds known as isoflavonoid o-glycosides. These are o-glycosylated derivatives of isoflavonoids, which are natural products derived from 3-phenylchromen-4-one. |
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Kingdom | Organic compounds |
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Super Class | Phenylpropanoids and polyketides |
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Class | Isoflavonoids |
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Sub Class | Isoflavonoid O-glycosides |
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Direct Parent | Isoflavonoid O-glycosides |
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Alternative Parents | |
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Substituents | - Isoflavonoid-7-o-glycoside
- Isoflavonoid o-glycoside
- 4p-o-methylisoflavone
- Isoflavone
- Phenolic glycoside
- O-glycosyl compound
- P-hydroxybenzoic acid alkyl ester
- P-hydroxybenzoic acid ester
- Chromone
- Glycosyl compound
- Benzopyran
- Benzoate ester
- 1-benzopyran
- Benzoic acid or derivatives
- Benzoyl
- Phenoxy compound
- Phenol ether
- Anisole
- Methoxybenzene
- Alkyl aryl ether
- 1-hydroxy-2-unsubstituted benzenoid
- Pyranone
- Phenol
- Monocyclic benzene moiety
- Benzenoid
- Pyran
- Monosaccharide
- Oxane
- Heteroaromatic compound
- Carboxylic acid ester
- Secondary alcohol
- Acetal
- Oxacycle
- Organoheterocyclic compound
- Monocarboxylic acid or derivatives
- Carboxylic acid derivative
- Ether
- Organic oxygen compound
- Alcohol
- Primary alcohol
- Organooxygen compound
- Organic oxide
- Hydrocarbon derivative
- Aromatic heteropolycyclic compound
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Molecular Framework | Aromatic heteropolycyclic compounds |
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External Descriptors | Not Available |
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Ontology |
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Physiological effect | Not Available |
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Disposition | |
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Process | Not Available |
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Role | |
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Physical Properties |
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State | Not Available |
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Experimental Molecular Properties | Property | Value | Reference |
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Melting Point | Not Available | Not Available | Boiling Point | Not Available | Not Available | Water Solubility | Not Available | Not Available | LogP | Not Available | Not Available |
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Experimental Chromatographic Properties | Not Available |
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Predicted Molecular Properties | |
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Predicted Chromatographic Properties | Predicted Collision Cross SectionsPredicted Kovats Retention IndicesUnderivatizedDerivatizedDerivative Name / Structure | SMILES | Kovats RI Value | Column Type | Reference |
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Formononetin 7-(2-p-hydroxybenzoylglucoside),1TMS,isomer #1 | COC1=CC=C(C2=COC3=CC(OC4OC(CO[Si](C)(C)C)C(O)C(O)C4OC(=O)C4=CC=C(O)C=C4)=CC=C3C2=O)C=C1 | 5240.9 | Semi standard non polar | 33892256 | Formononetin 7-(2-p-hydroxybenzoylglucoside),1TMS,isomer #2 | COC1=CC=C(C2=COC3=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4OC(=O)C4=CC=C(O)C=C4)=CC=C3C2=O)C=C1 | 5206.9 | Semi standard non polar | 33892256 | Formononetin 7-(2-p-hydroxybenzoylglucoside),1TMS,isomer #3 | COC1=CC=C(C2=COC3=CC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4OC(=O)C4=CC=C(O)C=C4)=CC=C3C2=O)C=C1 | 5227.6 | Semi standard non polar | 33892256 | Formononetin 7-(2-p-hydroxybenzoylglucoside),1TMS,isomer #4 | COC1=CC=C(C2=COC3=CC(OC4OC(CO)C(O)C(O)C4OC(=O)C4=CC=C(O[Si](C)(C)C)C=C4)=CC=C3C2=O)C=C1 | 5238.6 | Semi standard non polar | 33892256 | Formononetin 7-(2-p-hydroxybenzoylglucoside),2TMS,isomer #1 | COC1=CC=C(C2=COC3=CC(OC4OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C4OC(=O)C4=CC=C(O)C=C4)=CC=C3C2=O)C=C1 | 5075.1 | Semi standard non polar | 33892256 | Formononetin 7-(2-p-hydroxybenzoylglucoside),2TMS,isomer #2 | COC1=CC=C(C2=COC3=CC(OC4OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C4OC(=O)C4=CC=C(O)C=C4)=CC=C3C2=O)C=C1 | 5076.1 | Semi standard non polar | 33892256 | Formononetin 7-(2-p-hydroxybenzoylglucoside),2TMS,isomer #3 | COC1=CC=C(C2=COC3=CC(OC4OC(CO[Si](C)(C)C)C(O)C(O)C4OC(=O)C4=CC=C(O[Si](C)(C)C)C=C4)=CC=C3C2=O)C=C1 | 5046.9 | Semi standard non polar | 33892256 | Formononetin 7-(2-p-hydroxybenzoylglucoside),2TMS,isomer #4 | COC1=CC=C(C2=COC3=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4OC(=O)C4=CC=C(O)C=C4)=CC=C3C2=O)C=C1 | 5015.4 | Semi standard non polar | 33892256 | Formononetin 7-(2-p-hydroxybenzoylglucoside),2TMS,isomer #5 | COC1=CC=C(C2=COC3=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4OC(=O)C4=CC=C(O[Si](C)(C)C)C=C4)=CC=C3C2=O)C=C1 | 4991.1 | Semi standard non polar | 33892256 | Formononetin 7-(2-p-hydroxybenzoylglucoside),2TMS,isomer #6 | COC1=CC=C(C2=COC3=CC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4OC(=O)C4=CC=C(O[Si](C)(C)C)C=C4)=CC=C3C2=O)C=C1 | 5010.5 | Semi standard non polar | 33892256 | Formononetin 7-(2-p-hydroxybenzoylglucoside),3TMS,isomer #1 | COC1=CC=C(C2=COC3=CC(OC4OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4OC(=O)C4=CC=C(O)C=C4)=CC=C3C2=O)C=C1 | 4942.2 | Semi standard non polar | 33892256 | Formononetin 7-(2-p-hydroxybenzoylglucoside),3TMS,isomer #2 | COC1=CC=C(C2=COC3=CC(OC4OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C4OC(=O)C4=CC=C(O[Si](C)(C)C)C=C4)=CC=C3C2=O)C=C1 | 4884.4 | Semi standard non polar | 33892256 | Formononetin 7-(2-p-hydroxybenzoylglucoside),3TMS,isomer #3 | COC1=CC=C(C2=COC3=CC(OC4OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C4OC(=O)C4=CC=C(O[Si](C)(C)C)C=C4)=CC=C3C2=O)C=C1 | 4878.7 | Semi standard non polar | 33892256 | Formononetin 7-(2-p-hydroxybenzoylglucoside),3TMS,isomer #4 | COC1=CC=C(C2=COC3=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4OC(=O)C4=CC=C(O[Si](C)(C)C)C=C4)=CC=C3C2=O)C=C1 | 4835.9 | Semi standard non polar | 33892256 | Formononetin 7-(2-p-hydroxybenzoylglucoside),4TMS,isomer #1 | COC1=CC=C(C2=COC3=CC(OC4OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4OC(=O)C4=CC=C(O[Si](C)(C)C)C=C4)=CC=C3C2=O)C=C1 | 4775.3 | Semi standard non polar | 33892256 | Formononetin 7-(2-p-hydroxybenzoylglucoside),1TBDMS,isomer #1 | COC1=CC=C(C2=COC3=CC(OC4OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C4OC(=O)C4=CC=C(O)C=C4)=CC=C3C2=O)C=C1 | 5484.7 | Semi standard non polar | 33892256 | Formononetin 7-(2-p-hydroxybenzoylglucoside),1TBDMS,isomer #2 | COC1=CC=C(C2=COC3=CC(OC4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C4OC(=O)C4=CC=C(O)C=C4)=CC=C3C2=O)C=C1 | 5471.7 | Semi standard non polar | 33892256 | Formononetin 7-(2-p-hydroxybenzoylglucoside),1TBDMS,isomer #3 | COC1=CC=C(C2=COC3=CC(OC4OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C4OC(=O)C4=CC=C(O)C=C4)=CC=C3C2=O)C=C1 | 5487.2 | Semi standard non polar | 33892256 | Formononetin 7-(2-p-hydroxybenzoylglucoside),1TBDMS,isomer #4 | COC1=CC=C(C2=COC3=CC(OC4OC(CO)C(O)C(O)C4OC(=O)C4=CC=C(O[Si](C)(C)C(C)(C)C)C=C4)=CC=C3C2=O)C=C1 | 5451.1 | Semi standard non polar | 33892256 | Formononetin 7-(2-p-hydroxybenzoylglucoside),2TBDMS,isomer #1 | COC1=CC=C(C2=COC3=CC(OC4OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C4OC(=O)C4=CC=C(O)C=C4)=CC=C3C2=O)C=C1 | 5568.5 | Semi standard non polar | 33892256 | Formononetin 7-(2-p-hydroxybenzoylglucoside),2TBDMS,isomer #2 | COC1=CC=C(C2=COC3=CC(OC4OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C4OC(=O)C4=CC=C(O)C=C4)=CC=C3C2=O)C=C1 | 5570.3 | Semi standard non polar | 33892256 | Formononetin 7-(2-p-hydroxybenzoylglucoside),2TBDMS,isomer #3 | COC1=CC=C(C2=COC3=CC(OC4OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C4OC(=O)C4=CC=C(O[Si](C)(C)C(C)(C)C)C=C4)=CC=C3C2=O)C=C1 | 5539.4 | Semi standard non polar | 33892256 | Formononetin 7-(2-p-hydroxybenzoylglucoside),2TBDMS,isomer #4 | COC1=CC=C(C2=COC3=CC(OC4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C4OC(=O)C4=CC=C(O)C=C4)=CC=C3C2=O)C=C1 | 5544.2 | Semi standard non polar | 33892256 | Formononetin 7-(2-p-hydroxybenzoylglucoside),2TBDMS,isomer #5 | COC1=CC=C(C2=COC3=CC(OC4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C4OC(=O)C4=CC=C(O[Si](C)(C)C(C)(C)C)C=C4)=CC=C3C2=O)C=C1 | 5514.0 | Semi standard non polar | 33892256 | Formononetin 7-(2-p-hydroxybenzoylglucoside),2TBDMS,isomer #6 | COC1=CC=C(C2=COC3=CC(OC4OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C4OC(=O)C4=CC=C(O[Si](C)(C)C(C)(C)C)C=C4)=CC=C3C2=O)C=C1 | 5533.4 | Semi standard non polar | 33892256 | Formononetin 7-(2-p-hydroxybenzoylglucoside),3TBDMS,isomer #1 | COC1=CC=C(C2=COC3=CC(OC4OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C4OC(=O)C4=CC=C(O)C=C4)=CC=C3C2=O)C=C1 | 5611.8 | Semi standard non polar | 33892256 | Formononetin 7-(2-p-hydroxybenzoylglucoside),3TBDMS,isomer #2 | COC1=CC=C(C2=COC3=CC(OC4OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C4OC(=O)C4=CC=C(O[Si](C)(C)C(C)(C)C)C=C4)=CC=C3C2=O)C=C1 | 5597.6 | Semi standard non polar | 33892256 | Formononetin 7-(2-p-hydroxybenzoylglucoside),3TBDMS,isomer #3 | COC1=CC=C(C2=COC3=CC(OC4OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C4OC(=O)C4=CC=C(O[Si](C)(C)C(C)(C)C)C=C4)=CC=C3C2=O)C=C1 | 5593.5 | Semi standard non polar | 33892256 | Formononetin 7-(2-p-hydroxybenzoylglucoside),3TBDMS,isomer #4 | COC1=CC=C(C2=COC3=CC(OC4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C4OC(=O)C4=CC=C(O[Si](C)(C)C(C)(C)C)C=C4)=CC=C3C2=O)C=C1 | 5557.8 | Semi standard non polar | 33892256 |
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| GC-MS SpectraSpectrum Type | Description | Splash Key | Deposition Date | Source | View |
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Predicted GC-MS | Predicted GC-MS Spectrum - Formononetin 7-(2-p-hydroxybenzoylglucoside) GC-MS (Non-derivatized) - 70eV, Positive | splash10-00di-9340320000-cc406e371569924eb035 | 2017-09-01 | Wishart Lab | View Spectrum | Predicted GC-MS | Predicted GC-MS Spectrum - Formononetin 7-(2-p-hydroxybenzoylglucoside) GC-MS (2 TMS) - 70eV, Positive | splash10-0100-4891268000-3a73c97f95ae3e477c4b | 2017-10-06 | Wishart Lab | View Spectrum | Predicted GC-MS | Predicted GC-MS Spectrum - Formononetin 7-(2-p-hydroxybenzoylglucoside) GC-MS ("Formononetin 7-(2-p-hydroxybenzoylglucoside),1TMS,#1" TMS) - 70eV, Positive | Not Available | 2021-10-14 | Wishart Lab | View Spectrum | Predicted GC-MS | Predicted GC-MS Spectrum - Formononetin 7-(2-p-hydroxybenzoylglucoside) GC-MS (TMS_1_1) - 70eV, Positive | Not Available | 2021-10-15 | Wishart Lab | View Spectrum | Predicted GC-MS | Predicted GC-MS Spectrum - Formononetin 7-(2-p-hydroxybenzoylglucoside) GC-MS (TMS_1_2) - 70eV, Positive | Not Available | 2021-10-15 | Wishart Lab | View Spectrum | Predicted GC-MS | Predicted GC-MS Spectrum - Formononetin 7-(2-p-hydroxybenzoylglucoside) GC-MS (TMS_1_3) - 70eV, Positive | Not Available | 2021-10-15 | Wishart Lab | View Spectrum | Predicted GC-MS | Predicted GC-MS Spectrum - Formononetin 7-(2-p-hydroxybenzoylglucoside) GC-MS (TMS_1_4) - 70eV, Positive | Not Available | 2021-10-15 | Wishart Lab | View Spectrum | Predicted GC-MS | Predicted GC-MS Spectrum - Formononetin 7-(2-p-hydroxybenzoylglucoside) GC-MS (TMS_2_2) - 70eV, Positive | Not Available | 2021-10-15 | Wishart Lab | View Spectrum | Predicted GC-MS | Predicted GC-MS Spectrum - Formononetin 7-(2-p-hydroxybenzoylglucoside) GC-MS (TMS_2_3) - 70eV, Positive | Not Available | 2021-10-15 | Wishart Lab | View Spectrum | Predicted GC-MS | Predicted GC-MS Spectrum - Formononetin 7-(2-p-hydroxybenzoylglucoside) GC-MS (TMS_2_4) - 70eV, Positive | Not Available | 2021-10-15 | Wishart Lab | View Spectrum | Predicted GC-MS | Predicted GC-MS Spectrum - Formononetin 7-(2-p-hydroxybenzoylglucoside) GC-MS (TMS_2_5) - 70eV, Positive | Not Available | 2021-10-15 | Wishart Lab | View Spectrum | Predicted GC-MS | Predicted GC-MS Spectrum - Formononetin 7-(2-p-hydroxybenzoylglucoside) GC-MS (TMS_2_6) - 70eV, Positive | Not Available | 2021-10-15 | Wishart Lab | View Spectrum | Predicted GC-MS | Predicted GC-MS Spectrum - Formononetin 7-(2-p-hydroxybenzoylglucoside) GC-MS (TMS_3_1) - 70eV, Positive | Not Available | 2021-10-15 | Wishart Lab | View Spectrum | Predicted GC-MS | Predicted GC-MS Spectrum - Formononetin 7-(2-p-hydroxybenzoylglucoside) GC-MS (TMS_3_2) - 70eV, Positive | Not Available | 2021-10-15 | Wishart Lab | View Spectrum | Predicted GC-MS | Predicted GC-MS Spectrum - Formononetin 7-(2-p-hydroxybenzoylglucoside) GC-MS (TMS_3_3) - 70eV, Positive | Not Available | 2021-10-15 | Wishart Lab | View Spectrum | Predicted GC-MS | Predicted GC-MS Spectrum - Formononetin 7-(2-p-hydroxybenzoylglucoside) GC-MS (TMS_3_4) - 70eV, Positive | Not Available | 2021-10-15 | Wishart Lab | View Spectrum | Predicted GC-MS | Predicted GC-MS Spectrum - Formononetin 7-(2-p-hydroxybenzoylglucoside) GC-MS (TMS_4_1) - 70eV, Positive | Not Available | 2021-10-15 | Wishart Lab | View Spectrum | Predicted GC-MS | Predicted GC-MS Spectrum - Formononetin 7-(2-p-hydroxybenzoylglucoside) GC-MS (TBDMS_1_1) - 70eV, Positive | Not Available | 2021-10-15 | Wishart Lab | View Spectrum | Predicted GC-MS | Predicted GC-MS Spectrum - Formononetin 7-(2-p-hydroxybenzoylglucoside) GC-MS (TBDMS_1_2) - 70eV, Positive | Not Available | 2021-10-15 | Wishart Lab | View Spectrum | Predicted GC-MS | Predicted GC-MS Spectrum - Formononetin 7-(2-p-hydroxybenzoylglucoside) GC-MS (TBDMS_1_3) - 70eV, Positive | Not Available | 2021-10-15 | Wishart Lab | View Spectrum | Predicted GC-MS | Predicted GC-MS Spectrum - Formononetin 7-(2-p-hydroxybenzoylglucoside) GC-MS (TBDMS_1_4) - 70eV, Positive | Not Available | 2021-10-15 | Wishart Lab | View Spectrum | Predicted GC-MS | Predicted GC-MS Spectrum - Formononetin 7-(2-p-hydroxybenzoylglucoside) GC-MS (TBDMS_2_1) - 70eV, Positive | Not Available | 2021-10-15 | Wishart Lab | View Spectrum | Predicted GC-MS | Predicted GC-MS Spectrum - Formononetin 7-(2-p-hydroxybenzoylglucoside) GC-MS (TBDMS_2_2) - 70eV, Positive | Not Available | 2021-10-15 | Wishart Lab | View Spectrum | Predicted GC-MS | Predicted GC-MS Spectrum - Formononetin 7-(2-p-hydroxybenzoylglucoside) GC-MS (TBDMS_2_3) - 70eV, Positive | Not Available | 2021-10-15 | Wishart Lab | View Spectrum | Predicted GC-MS | Predicted GC-MS Spectrum - Formononetin 7-(2-p-hydroxybenzoylglucoside) GC-MS (TBDMS_2_4) - 70eV, Positive | Not Available | 2021-10-15 | Wishart Lab | View Spectrum |
MS/MS SpectraSpectrum Type | Description | Splash Key | Deposition Date | Source | View |
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Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Formononetin 7-(2-p-hydroxybenzoylglucoside) 10V, Positive-QTOF | splash10-014i-0390250000-5c31d9d0c46a92f54662 | 2016-08-03 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Formononetin 7-(2-p-hydroxybenzoylglucoside) 20V, Positive-QTOF | splash10-014i-0190000000-4d3fa294c9022ce88d14 | 2016-08-03 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Formononetin 7-(2-p-hydroxybenzoylglucoside) 40V, Positive-QTOF | splash10-01b9-3690000000-2bfb27297718c2aebf4e | 2016-08-03 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Formononetin 7-(2-p-hydroxybenzoylglucoside) 10V, Negative-QTOF | splash10-00kk-2580590000-9b5681e7ea8cd8e3c8b2 | 2016-08-03 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Formononetin 7-(2-p-hydroxybenzoylglucoside) 20V, Negative-QTOF | splash10-014r-3590110000-1eb3fc512535feab3b45 | 2016-08-03 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Formononetin 7-(2-p-hydroxybenzoylglucoside) 40V, Negative-QTOF | splash10-014u-9880000000-3a4a3c3902579d4d7570 | 2016-08-03 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Formononetin 7-(2-p-hydroxybenzoylglucoside) 10V, Negative-QTOF | splash10-0002-0020090000-23ab41d1fd60935cb9d6 | 2021-09-22 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Formononetin 7-(2-p-hydroxybenzoylglucoside) 20V, Negative-QTOF | splash10-014i-2391340000-2115cd0a2b53077916ae | 2021-09-22 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Formononetin 7-(2-p-hydroxybenzoylglucoside) 40V, Negative-QTOF | splash10-0006-9420010000-fcf418c6a71d86660934 | 2021-09-22 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Formononetin 7-(2-p-hydroxybenzoylglucoside) 10V, Positive-QTOF | splash10-0uxr-0180090000-c4d59861e0619ba930a9 | 2021-09-22 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Formononetin 7-(2-p-hydroxybenzoylglucoside) 20V, Positive-QTOF | splash10-01ba-5491650000-987f155084f67161b6b3 | 2021-09-22 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Formononetin 7-(2-p-hydroxybenzoylglucoside) 40V, Positive-QTOF | splash10-05fu-9422230000-22d4cc61135bf436f25f | 2021-09-22 | Wishart Lab | View Spectrum |
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