Record Information |
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Version | 5.0 |
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Status | Expected but not Quantified |
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Creation Date | 2012-09-11 23:23:44 UTC |
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Update Date | 2022-03-07 02:55:38 UTC |
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HMDB ID | HMDB0038111 |
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Secondary Accession Numbers | |
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Metabolite Identification |
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Common Name | Kievitone hydrate |
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Description | Kievitone hydrate belongs to the class of organic compounds known as 8-prenylated isoflavanones. These are isoflavanones featuring a C5-isoprenoid unit at the 8-position. Kievitone hydrate has been detected, but not quantified in, a few different foods, such as gram beans (Vigna mungo), lima beans (Phaseolus lunatus), and pulses. This could make kievitone hydrate a potential biomarker for the consumption of these foods. Based on a literature review very few articles have been published on Kievitone hydrate. |
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Structure | CC(C)(O)CCC1=C2OCC(C(=O)C2=C(O)C=C1O)C1=C(O)C=C(O)C=C1 InChI=1S/C20H22O7/c1-20(2,26)6-5-12-15(23)8-16(24)17-18(25)13(9-27-19(12)17)11-4-3-10(21)7-14(11)22/h3-4,7-8,13,21-24,26H,5-6,9H2,1-2H3 |
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Synonyms | Value | Source |
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Kievitone hydric acid | Generator |
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Chemical Formula | C20H22O7 |
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Average Molecular Weight | 374.3845 |
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Monoisotopic Molecular Weight | 374.136553058 |
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IUPAC Name | 3-(2,4-dihydroxyphenyl)-5,7-dihydroxy-8-(3-hydroxy-3-methylbutyl)-3,4-dihydro-2H-1-benzopyran-4-one |
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Traditional Name | kievitone hydrate |
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CAS Registry Number | 62682-11-5 |
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SMILES | CC(C)(O)CCC1=C2OCC(C(=O)C2=C(O)C=C1O)C1=C(O)C=C(O)C=C1 |
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InChI Identifier | InChI=1S/C20H22O7/c1-20(2,26)6-5-12-15(23)8-16(24)17-18(25)13(9-27-19(12)17)11-4-3-10(21)7-14(11)22/h3-4,7-8,13,21-24,26H,5-6,9H2,1-2H3 |
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InChI Key | QISUKJAAXYVLMA-UHFFFAOYSA-N |
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Chemical Taxonomy |
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Description | Belongs to the class of organic compounds known as 8-prenylated isoflavanones. These are isoflavanones featuring a C5-isoprenoid unit at the 8-position. |
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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 | Isoflavans |
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Direct Parent | 8-prenylated isoflavanones |
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Alternative Parents | |
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Substituents | - 8-prenylated isoflavanone
- Isoflavanol
- Hydroxyisoflavonoid
- Chromone
- 1-benzopyran
- Chromane
- Benzopyran
- Resorcinol
- Aryl ketone
- Aryl alkyl ketone
- 1-hydroxy-4-unsubstituted benzenoid
- Alkyl aryl ether
- 1-hydroxy-2-unsubstituted benzenoid
- Phenol
- Benzenoid
- Monocyclic benzene moiety
- Tertiary alcohol
- Vinylogous acid
- Ketone
- Oxacycle
- Organoheterocyclic compound
- Ether
- Alcohol
- Hydrocarbon derivative
- Organic oxide
- Organic oxygen compound
- Organooxygen compound
- Aromatic heteropolycyclic compound
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Molecular Framework | Aromatic heteropolycyclic compounds |
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External Descriptors | |
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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 | 129.8 mg/L @ 25 °C (est) | The Good Scents Company Information System | 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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Kievitone hydrate,1TMS,isomer #1 | CC(C)(CCC1=C(O)C=C(O)C2=C1OCC(C1=CC=C(O)C=C1O)C2=O)O[Si](C)(C)C | 3467.5 | Semi standard non polar | 33892256 | Kievitone hydrate,1TMS,isomer #2 | CC(C)(O)CCC1=C(O)C=C(O[Si](C)(C)C)C2=C1OCC(C1=CC=C(O)C=C1O)C2=O | 3380.8 | Semi standard non polar | 33892256 | Kievitone hydrate,1TMS,isomer #3 | CC(C)(O)CCC1=C(O[Si](C)(C)C)C=C(O)C2=C1OCC(C1=CC=C(O)C=C1O)C2=O | 3318.3 | Semi standard non polar | 33892256 | Kievitone hydrate,1TMS,isomer #4 | CC(C)(O)CCC1=C(O)C=C(O)C2=C1OCC(C1=CC=C(O)C=C1O[Si](C)(C)C)C2=O | 3325.6 | Semi standard non polar | 33892256 | Kievitone hydrate,1TMS,isomer #5 | CC(C)(O)CCC1=C(O)C=C(O)C2=C1OCC(C1=CC=C(O[Si](C)(C)C)C=C1O)C2=O | 3309.0 | Semi standard non polar | 33892256 | Kievitone hydrate,2TMS,isomer #1 | CC(C)(CCC1=C(O[Si](C)(C)C)C=C(O)C2=C1OCC(C1=CC=C(O)C=C1O)C2=O)O[Si](C)(C)C | 3350.0 | Semi standard non polar | 33892256 | Kievitone hydrate,2TMS,isomer #10 | CC(C)(O)CCC1=C(O)C=C(O)C2=C1OCC(C1=CC=C(O[Si](C)(C)C)C=C1O[Si](C)(C)C)C2=O | 3188.8 | Semi standard non polar | 33892256 | Kievitone hydrate,2TMS,isomer #2 | CC(C)(CCC1=C(O)C=C(O[Si](C)(C)C)C2=C1OCC(C1=CC=C(O)C=C1O)C2=O)O[Si](C)(C)C | 3437.9 | Semi standard non polar | 33892256 | Kievitone hydrate,2TMS,isomer #3 | CC(C)(CCC1=C(O)C=C(O)C2=C1OCC(C1=CC=C(O[Si](C)(C)C)C=C1O)C2=O)O[Si](C)(C)C | 3334.2 | Semi standard non polar | 33892256 | Kievitone hydrate,2TMS,isomer #4 | CC(C)(CCC1=C(O)C=C(O)C2=C1OCC(C1=CC=C(O)C=C1O[Si](C)(C)C)C2=O)O[Si](C)(C)C | 3360.6 | Semi standard non polar | 33892256 | Kievitone hydrate,2TMS,isomer #5 | CC(C)(O)CCC1=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C2=C1OCC(C1=CC=C(O)C=C1O)C2=O | 3270.2 | Semi standard non polar | 33892256 | Kievitone hydrate,2TMS,isomer #6 | CC(C)(O)CCC1=C(O)C=C(O[Si](C)(C)C)C2=C1OCC(C1=CC=C(O[Si](C)(C)C)C=C1O)C2=O | 3255.4 | Semi standard non polar | 33892256 | Kievitone hydrate,2TMS,isomer #7 | CC(C)(O)CCC1=C(O)C=C(O[Si](C)(C)C)C2=C1OCC(C1=CC=C(O)C=C1O[Si](C)(C)C)C2=O | 3283.5 | Semi standard non polar | 33892256 | Kievitone hydrate,2TMS,isomer #8 | CC(C)(O)CCC1=C(O[Si](C)(C)C)C=C(O)C2=C1OCC(C1=CC=C(O[Si](C)(C)C)C=C1O)C2=O | 3188.2 | Semi standard non polar | 33892256 | Kievitone hydrate,2TMS,isomer #9 | CC(C)(O)CCC1=C(O[Si](C)(C)C)C=C(O)C2=C1OCC(C1=CC=C(O)C=C1O[Si](C)(C)C)C2=O | 3208.1 | Semi standard non polar | 33892256 | Kievitone hydrate,3TMS,isomer #1 | CC(C)(CCC1=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C2=C1OCC(C1=CC=C(O)C=C1O)C2=O)O[Si](C)(C)C | 3297.4 | Semi standard non polar | 33892256 | Kievitone hydrate,3TMS,isomer #10 | CC(C)(O)CCC1=C(O[Si](C)(C)C)C=C(O)C2=C1OCC(C1=CC=C(O[Si](C)(C)C)C=C1O[Si](C)(C)C)C2=O | 3138.0 | Semi standard non polar | 33892256 | Kievitone hydrate,3TMS,isomer #2 | CC(C)(CCC1=C(O[Si](C)(C)C)C=C(O)C2=C1OCC(C1=CC=C(O[Si](C)(C)C)C=C1O)C2=O)O[Si](C)(C)C | 3212.1 | Semi standard non polar | 33892256 | Kievitone hydrate,3TMS,isomer #3 | CC(C)(CCC1=C(O[Si](C)(C)C)C=C(O)C2=C1OCC(C1=CC=C(O)C=C1O[Si](C)(C)C)C2=O)O[Si](C)(C)C | 3220.7 | Semi standard non polar | 33892256 | Kievitone hydrate,3TMS,isomer #4 | CC(C)(CCC1=C(O)C=C(O[Si](C)(C)C)C2=C1OCC(C1=CC=C(O[Si](C)(C)C)C=C1O)C2=O)O[Si](C)(C)C | 3284.6 | Semi standard non polar | 33892256 | Kievitone hydrate,3TMS,isomer #5 | CC(C)(CCC1=C(O)C=C(O[Si](C)(C)C)C2=C1OCC(C1=CC=C(O)C=C1O[Si](C)(C)C)C2=O)O[Si](C)(C)C | 3308.4 | Semi standard non polar | 33892256 | Kievitone hydrate,3TMS,isomer #6 | CC(C)(CCC1=C(O)C=C(O)C2=C1OCC(C1=CC=C(O[Si](C)(C)C)C=C1O[Si](C)(C)C)C2=O)O[Si](C)(C)C | 3220.2 | Semi standard non polar | 33892256 | Kievitone hydrate,3TMS,isomer #7 | CC(C)(O)CCC1=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C2=C1OCC(C1=CC=C(O[Si](C)(C)C)C=C1O)C2=O | 3170.5 | Semi standard non polar | 33892256 | Kievitone hydrate,3TMS,isomer #8 | CC(C)(O)CCC1=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C2=C1OCC(C1=CC=C(O)C=C1O[Si](C)(C)C)C2=O | 3177.8 | Semi standard non polar | 33892256 | Kievitone hydrate,3TMS,isomer #9 | CC(C)(O)CCC1=C(O)C=C(O[Si](C)(C)C)C2=C1OCC(C1=CC=C(O[Si](C)(C)C)C=C1O[Si](C)(C)C)C2=O | 3182.5 | Semi standard non polar | 33892256 | Kievitone hydrate,4TMS,isomer #1 | CC(C)(CCC1=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C2=C1OCC(C1=CC=C(O[Si](C)(C)C)C=C1O)C2=O)O[Si](C)(C)C | 3215.0 | Semi standard non polar | 33892256 | Kievitone hydrate,4TMS,isomer #2 | CC(C)(CCC1=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C2=C1OCC(C1=CC=C(O)C=C1O[Si](C)(C)C)C2=O)O[Si](C)(C)C | 3211.2 | Semi standard non polar | 33892256 | Kievitone hydrate,4TMS,isomer #3 | CC(C)(CCC1=C(O[Si](C)(C)C)C=C(O)C2=C1OCC(C1=CC=C(O[Si](C)(C)C)C=C1O[Si](C)(C)C)C2=O)O[Si](C)(C)C | 3192.2 | Semi standard non polar | 33892256 | Kievitone hydrate,4TMS,isomer #4 | CC(C)(CCC1=C(O)C=C(O[Si](C)(C)C)C2=C1OCC(C1=CC=C(O[Si](C)(C)C)C=C1O[Si](C)(C)C)C2=O)O[Si](C)(C)C | 3217.4 | Semi standard non polar | 33892256 | Kievitone hydrate,4TMS,isomer #5 | CC(C)(O)CCC1=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C2=C1OCC(C1=CC=C(O[Si](C)(C)C)C=C1O[Si](C)(C)C)C2=O | 3128.9 | Semi standard non polar | 33892256 | Kievitone hydrate,5TMS,isomer #1 | CC(C)(CCC1=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C2=C1OCC(C1=CC=C(O[Si](C)(C)C)C=C1O[Si](C)(C)C)C2=O)O[Si](C)(C)C | 3203.4 | Semi standard non polar | 33892256 | Kievitone hydrate,1TBDMS,isomer #1 | CC(C)(CCC1=C(O)C=C(O)C2=C1OCC(C1=CC=C(O)C=C1O)C2=O)O[Si](C)(C)C(C)(C)C | 3734.2 | Semi standard non polar | 33892256 | Kievitone hydrate,1TBDMS,isomer #2 | CC(C)(O)CCC1=C(O)C=C(O[Si](C)(C)C(C)(C)C)C2=C1OCC(C1=CC=C(O)C=C1O)C2=O | 3637.7 | Semi standard non polar | 33892256 | Kievitone hydrate,1TBDMS,isomer #3 | CC(C)(O)CCC1=C(O[Si](C)(C)C(C)(C)C)C=C(O)C2=C1OCC(C1=CC=C(O)C=C1O)C2=O | 3576.6 | Semi standard non polar | 33892256 | Kievitone hydrate,1TBDMS,isomer #4 | CC(C)(O)CCC1=C(O)C=C(O)C2=C1OCC(C1=CC=C(O)C=C1O[Si](C)(C)C(C)(C)C)C2=O | 3582.0 | Semi standard non polar | 33892256 | Kievitone hydrate,1TBDMS,isomer #5 | CC(C)(O)CCC1=C(O)C=C(O)C2=C1OCC(C1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1O)C2=O | 3575.7 | Semi standard non polar | 33892256 | Kievitone hydrate,2TBDMS,isomer #1 | CC(C)(CCC1=C(O[Si](C)(C)C(C)(C)C)C=C(O)C2=C1OCC(C1=CC=C(O)C=C1O)C2=O)O[Si](C)(C)C(C)(C)C | 3845.6 | Semi standard non polar | 33892256 | Kievitone hydrate,2TBDMS,isomer #10 | CC(C)(O)CCC1=C(O)C=C(O)C2=C1OCC(C1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1O[Si](C)(C)C(C)(C)C)C2=O | 3698.8 | Semi standard non polar | 33892256 | Kievitone hydrate,2TBDMS,isomer #2 | CC(C)(CCC1=C(O)C=C(O[Si](C)(C)C(C)(C)C)C2=C1OCC(C1=CC=C(O)C=C1O)C2=O)O[Si](C)(C)C(C)(C)C | 3932.0 | Semi standard non polar | 33892256 | Kievitone hydrate,2TBDMS,isomer #3 | CC(C)(CCC1=C(O)C=C(O)C2=C1OCC(C1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1O)C2=O)O[Si](C)(C)C(C)(C)C | 3870.3 | Semi standard non polar | 33892256 | Kievitone hydrate,2TBDMS,isomer #4 | CC(C)(CCC1=C(O)C=C(O)C2=C1OCC(C1=CC=C(O)C=C1O[Si](C)(C)C(C)(C)C)C2=O)O[Si](C)(C)C(C)(C)C | 3858.4 | Semi standard non polar | 33892256 | Kievitone hydrate,2TBDMS,isomer #5 | CC(C)(O)CCC1=C(O[Si](C)(C)C(C)(C)C)C=C(O[Si](C)(C)C(C)(C)C)C2=C1OCC(C1=CC=C(O)C=C1O)C2=O | 3736.6 | Semi standard non polar | 33892256 | Kievitone hydrate,2TBDMS,isomer #6 | CC(C)(O)CCC1=C(O)C=C(O[Si](C)(C)C(C)(C)C)C2=C1OCC(C1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1O)C2=O | 3763.0 | Semi standard non polar | 33892256 | Kievitone hydrate,2TBDMS,isomer #7 | CC(C)(O)CCC1=C(O)C=C(O[Si](C)(C)C(C)(C)C)C2=C1OCC(C1=CC=C(O)C=C1O[Si](C)(C)C(C)(C)C)C2=O | 3754.5 | Semi standard non polar | 33892256 | Kievitone hydrate,2TBDMS,isomer #8 | CC(C)(O)CCC1=C(O[Si](C)(C)C(C)(C)C)C=C(O)C2=C1OCC(C1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1O)C2=O | 3688.5 | Semi standard non polar | 33892256 | Kievitone hydrate,2TBDMS,isomer #9 | CC(C)(O)CCC1=C(O[Si](C)(C)C(C)(C)C)C=C(O)C2=C1OCC(C1=CC=C(O)C=C1O[Si](C)(C)C(C)(C)C)C2=O | 3673.0 | Semi standard non polar | 33892256 | Kievitone hydrate,3TBDMS,isomer #1 | CC(C)(CCC1=C(O[Si](C)(C)C(C)(C)C)C=C(O[Si](C)(C)C(C)(C)C)C2=C1OCC(C1=CC=C(O)C=C1O)C2=O)O[Si](C)(C)C(C)(C)C | 3982.7 | Semi standard non polar | 33892256 | Kievitone hydrate,3TBDMS,isomer #10 | CC(C)(O)CCC1=C(O[Si](C)(C)C(C)(C)C)C=C(O)C2=C1OCC(C1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1O[Si](C)(C)C(C)(C)C)C2=O | 3817.4 | Semi standard non polar | 33892256 | Kievitone hydrate,3TBDMS,isomer #2 | CC(C)(CCC1=C(O[Si](C)(C)C(C)(C)C)C=C(O)C2=C1OCC(C1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1O)C2=O)O[Si](C)(C)C(C)(C)C | 3948.2 | Semi standard non polar | 33892256 | Kievitone hydrate,3TBDMS,isomer #3 | CC(C)(CCC1=C(O[Si](C)(C)C(C)(C)C)C=C(O)C2=C1OCC(C1=CC=C(O)C=C1O[Si](C)(C)C(C)(C)C)C2=O)O[Si](C)(C)C(C)(C)C | 3910.4 | Semi standard non polar | 33892256 | Kievitone hydrate,3TBDMS,isomer #4 | CC(C)(CCC1=C(O)C=C(O[Si](C)(C)C(C)(C)C)C2=C1OCC(C1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1O)C2=O)O[Si](C)(C)C(C)(C)C | 4026.1 | Semi standard non polar | 33892256 | Kievitone hydrate,3TBDMS,isomer #5 | CC(C)(CCC1=C(O)C=C(O[Si](C)(C)C(C)(C)C)C2=C1OCC(C1=CC=C(O)C=C1O[Si](C)(C)C(C)(C)C)C2=O)O[Si](C)(C)C(C)(C)C | 4009.2 | Semi standard non polar | 33892256 | Kievitone hydrate,3TBDMS,isomer #6 | CC(C)(CCC1=C(O)C=C(O)C2=C1OCC(C1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1O[Si](C)(C)C(C)(C)C)C2=O)O[Si](C)(C)C(C)(C)C | 3957.2 | Semi standard non polar | 33892256 | Kievitone hydrate,3TBDMS,isomer #7 | CC(C)(O)CCC1=C(O[Si](C)(C)C(C)(C)C)C=C(O[Si](C)(C)C(C)(C)C)C2=C1OCC(C1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1O)C2=O | 3834.4 | Semi standard non polar | 33892256 | Kievitone hydrate,3TBDMS,isomer #8 | CC(C)(O)CCC1=C(O[Si](C)(C)C(C)(C)C)C=C(O[Si](C)(C)C(C)(C)C)C2=C1OCC(C1=CC=C(O)C=C1O[Si](C)(C)C(C)(C)C)C2=O | 3808.0 | Semi standard non polar | 33892256 | Kievitone hydrate,3TBDMS,isomer #9 | CC(C)(O)CCC1=C(O)C=C(O[Si](C)(C)C(C)(C)C)C2=C1OCC(C1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1O[Si](C)(C)C(C)(C)C)C2=O | 3854.6 | Semi standard non polar | 33892256 | Kievitone hydrate,4TBDMS,isomer #1 | CC(C)(CCC1=C(O[Si](C)(C)C(C)(C)C)C=C(O[Si](C)(C)C(C)(C)C)C2=C1OCC(C1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1O)C2=O)O[Si](C)(C)C(C)(C)C | 4075.2 | Semi standard non polar | 33892256 | Kievitone hydrate,4TBDMS,isomer #2 | CC(C)(CCC1=C(O[Si](C)(C)C(C)(C)C)C=C(O[Si](C)(C)C(C)(C)C)C2=C1OCC(C1=CC=C(O)C=C1O[Si](C)(C)C(C)(C)C)C2=O)O[Si](C)(C)C(C)(C)C | 4041.1 | Semi standard non polar | 33892256 | Kievitone hydrate,4TBDMS,isomer #3 | CC(C)(CCC1=C(O[Si](C)(C)C(C)(C)C)C=C(O)C2=C1OCC(C1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1O[Si](C)(C)C(C)(C)C)C2=O)O[Si](C)(C)C(C)(C)C | 4077.2 | Semi standard non polar | 33892256 | Kievitone hydrate,4TBDMS,isomer #4 | CC(C)(CCC1=C(O)C=C(O[Si](C)(C)C(C)(C)C)C2=C1OCC(C1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1O[Si](C)(C)C(C)(C)C)C2=O)O[Si](C)(C)C(C)(C)C | 4094.7 | Semi standard non polar | 33892256 | Kievitone hydrate,4TBDMS,isomer #5 | CC(C)(O)CCC1=C(O[Si](C)(C)C(C)(C)C)C=C(O[Si](C)(C)C(C)(C)C)C2=C1OCC(C1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1O[Si](C)(C)C(C)(C)C)C2=O | 3969.3 | 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 - Kievitone hydrate GC-MS (Non-derivatized) - 70eV, Positive | splash10-0pb9-5109000000-0fa595a0f7bbf7b86c01 | 2017-09-01 | Wishart Lab | View Spectrum | Predicted GC-MS | Predicted GC-MS Spectrum - Kievitone hydrate GC-MS (4 TMS) - 70eV, Positive | splash10-0002-4500049000-934994ffdc03c8134406 | 2017-10-06 | Wishart Lab | View Spectrum | Predicted GC-MS | Predicted GC-MS Spectrum - Kievitone hydrate GC-MS (Non-derivatized) - 70eV, Positive | Not Available | 2021-10-12 | 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 - Kievitone hydrate 10V, Positive-QTOF | splash10-0a4i-0019000000-1db2d0e002090b415c48 | 2015-04-24 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Kievitone hydrate 20V, Positive-QTOF | splash10-0q2i-2529000000-0262695fe9904ec9ccac | 2015-04-24 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Kievitone hydrate 40V, Positive-QTOF | splash10-00dr-1941000000-9031d633e6e6dabadb0f | 2015-04-24 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Kievitone hydrate 10V, Negative-QTOF | splash10-00di-0019000000-aad40787030581ca741d | 2015-04-25 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Kievitone hydrate 20V, Negative-QTOF | splash10-0ab9-0769000000-299f95ba6a85953fd0ff | 2015-04-25 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Kievitone hydrate 40V, Negative-QTOF | splash10-0a4i-3910000000-cfa2887049aae4c9d6ca | 2015-04-25 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Kievitone hydrate 10V, Negative-QTOF | splash10-00di-0009000000-f39c61ae3f4720a70671 | 2021-09-22 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Kievitone hydrate 20V, Negative-QTOF | splash10-00di-1049000000-7f16dcb844552561977a | 2021-09-22 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Kievitone hydrate 40V, Negative-QTOF | splash10-055n-5984000000-4d3eae8c1547c16fdb93 | 2021-09-22 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Kievitone hydrate 10V, Positive-QTOF | splash10-0a6s-0059000000-8e7f8bafb6a685716daa | 2021-09-23 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Kievitone hydrate 20V, Positive-QTOF | splash10-0kdr-2359000000-2a0ba666c904eca78066 | 2021-09-23 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Kievitone hydrate 40V, Positive-QTOF | splash10-0aor-4931000000-265785b9acb0971bc877 | 2021-09-23 | Wishart Lab | View Spectrum |
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