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 01:26:40 UTC |
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Update Date | 2022-03-07 02:56:23 UTC |
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HMDB ID | HMDB0039902 |
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Secondary Accession Numbers | |
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Metabolite Identification |
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Common Name | Dihydrodaidzin |
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Description | Dihydrodaidzin 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. Dihydrodaidzin has been detected, but not quantified in, several different foods, such as teas (Camellia sinensis), soy beans (Glycine max), fats and oils, green tea, and red tea. This could make dihydrodaidzin a potential biomarker for the consumption of these foods. Based on a literature review very few articles have been published on Dihydrodaidzin. |
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Structure | OC[C@H]1O[C@@H](OC2=CC3=C(C=C2)C(=O)C(CO3)C2=CC=C(O)C=C2)[C@H](O)[C@@H](O)[C@@H]1O InChI=1S/C21H22O9/c22-8-16-18(25)19(26)20(27)21(30-16)29-12-5-6-13-15(7-12)28-9-14(17(13)24)10-1-3-11(23)4-2-10/h1-7,14,16,18-23,25-27H,8-9H2/t14?,16-,18-,19+,20-,21-/m1/s1 |
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Synonyms | Value | Source |
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7,4'-Dihydroxyisoflavanone 7-O-glucoside | HMDB | Dihydrodaidzin | MeSH |
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Chemical Formula | C21H22O9 |
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Average Molecular Weight | 418.394 |
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Monoisotopic Molecular Weight | 418.126382302 |
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IUPAC Name | 3-(4-hydroxyphenyl)-7-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,4-dihydro-2H-1-benzopyran-4-one |
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Traditional Name | 3-(4-hydroxyphenyl)-7-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,3-dihydro-1-benzopyran-4-one |
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CAS Registry Number | Not Available |
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SMILES | OC[C@H]1O[C@@H](OC2=CC3=C(C=C2)C(=O)C(CO3)C2=CC=C(O)C=C2)[C@H](O)[C@@H](O)[C@@H]1O |
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InChI Identifier | InChI=1S/C21H22O9/c22-8-16-18(25)19(26)20(27)21(30-16)29-12-5-6-13-15(7-12)28-9-14(17(13)24)10-1-3-11(23)4-2-10/h1-7,14,16,18-23,25-27H,8-9H2/t14?,16-,18-,19+,20-,21-/m1/s1 |
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InChI Key | KKJXSJGKUZBVIH-RGHIGTIISA-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 o-glycoside
- Isoflavonoid-7-o-glycoside
- Isoflavanol
- Isoflavanone
- Isoflavan
- Phenolic glycoside
- Hexose monosaccharide
- Chromone
- Glycosyl compound
- O-glycosyl compound
- 1-benzopyran
- Benzopyran
- Chromane
- Aryl alkyl ketone
- Aryl ketone
- 1-hydroxy-2-unsubstituted benzenoid
- Phenol
- Alkyl aryl ether
- Oxane
- Monocyclic benzene moiety
- Benzenoid
- Monosaccharide
- Secondary alcohol
- Ketone
- Ether
- Acetal
- Oxacycle
- Organoheterocyclic compound
- Polyol
- Primary alcohol
- Alcohol
- Organic oxygen compound
- Organic oxide
- Hydrocarbon derivative
- Organooxygen compound
- 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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Dihydrodaidzin,1TMS,isomer #1 | C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=C3C(=O)C(C4=CC=C(O)C=C4)COC3=C2)[C@H](O)[C@@H](O)[C@@H]1O | 3819.3 | Semi standard non polar | 33892256 | Dihydrodaidzin,1TMS,isomer #2 | C[Si](C)(C)OC1=CC=C(C2COC3=CC(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)=CC=C3C2=O)C=C1 | 3882.1 | Semi standard non polar | 33892256 | Dihydrodaidzin,1TMS,isomer #3 | C[Si](C)(C)O[C@H]1[C@H](OC2=CC=C3C(=O)C(C4=CC=C(O)C=C4)COC3=C2)O[C@H](CO)[C@@H](O)[C@@H]1O | 3831.5 | Semi standard non polar | 33892256 | Dihydrodaidzin,1TMS,isomer #4 | C[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](OC2=CC=C3C(=O)C(C4=CC=C(O)C=C4)COC3=C2)O[C@H](CO)[C@H]1O | 3833.3 | Semi standard non polar | 33892256 | Dihydrodaidzin,1TMS,isomer #5 | C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](OC2=CC=C3C(=O)C(C4=CC=C(O)C=C4)COC3=C2)[C@H](O)[C@H]1O | 3823.0 | Semi standard non polar | 33892256 | Dihydrodaidzin,2TMS,isomer #1 | C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=C3C(=O)C(C4=CC=C(O[Si](C)(C)C)C=C4)COC3=C2)[C@H](O)[C@@H](O)[C@@H]1O | 3787.0 | Semi standard non polar | 33892256 | Dihydrodaidzin,2TMS,isomer #10 | C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](OC2=CC=C3C(=O)C(C4=CC=C(O)C=C4)COC3=C2)[C@H](O)[C@H]1O[Si](C)(C)C | 3742.3 | Semi standard non polar | 33892256 | Dihydrodaidzin,2TMS,isomer #2 | C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=C3C(=O)C(C4=CC=C(O)C=C4)COC3=C2)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O | 3749.9 | Semi standard non polar | 33892256 | Dihydrodaidzin,2TMS,isomer #3 | C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=C3C(=O)C(C4=CC=C(O)C=C4)COC3=C2)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O | 3735.3 | Semi standard non polar | 33892256 | Dihydrodaidzin,2TMS,isomer #4 | C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=C3C(=O)C(C4=CC=C(O)C=C4)COC3=C2)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C | 3763.6 | Semi standard non polar | 33892256 | Dihydrodaidzin,2TMS,isomer #5 | C[Si](C)(C)OC1=CC=C(C2COC3=CC(O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=CC=C3C2=O)C=C1 | 3793.0 | Semi standard non polar | 33892256 | Dihydrodaidzin,2TMS,isomer #6 | C[Si](C)(C)OC1=CC=C(C2COC3=CC(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=CC=C3C2=O)C=C1 | 3807.2 | Semi standard non polar | 33892256 | Dihydrodaidzin,2TMS,isomer #7 | C[Si](C)(C)OC1=CC=C(C2COC3=CC(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=CC=C3C2=O)C=C1 | 3806.5 | Semi standard non polar | 33892256 | Dihydrodaidzin,2TMS,isomer #8 | C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](OC2=CC=C3C(=O)C(C4=CC=C(O)C=C4)COC3=C2)O[C@@H]1CO | 3744.6 | Semi standard non polar | 33892256 | Dihydrodaidzin,2TMS,isomer #9 | C[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C)[C@H](OC2=CC=C3C(=O)C(C4=CC=C(O)C=C4)COC3=C2)O[C@H](CO)[C@H]1O | 3764.8 | Semi standard non polar | 33892256 | Dihydrodaidzin,3TMS,isomer #1 | C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=C3C(=O)C(C4=CC=C(O[Si](C)(C)C)C=C4)COC3=C2)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O | 3735.5 | Semi standard non polar | 33892256 | Dihydrodaidzin,3TMS,isomer #10 | C[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C)[C@H](OC2=CC=C3C(=O)C(C4=CC=C(O)C=C4)COC3=C2)O[C@H](CO)[C@H]1O[Si](C)(C)C | 3697.1 | Semi standard non polar | 33892256 | Dihydrodaidzin,3TMS,isomer #2 | C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=C3C(=O)C(C4=CC=C(O[Si](C)(C)C)C=C4)COC3=C2)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O | 3720.4 | Semi standard non polar | 33892256 | Dihydrodaidzin,3TMS,isomer #3 | C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=C3C(=O)C(C4=CC=C(O[Si](C)(C)C)C=C4)COC3=C2)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C | 3732.6 | Semi standard non polar | 33892256 | Dihydrodaidzin,3TMS,isomer #4 | C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=C3C(=O)C(C4=CC=C(O)C=C4)COC3=C2)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O | 3694.5 | Semi standard non polar | 33892256 | Dihydrodaidzin,3TMS,isomer #5 | C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=C3C(=O)C(C4=CC=C(O)C=C4)COC3=C2)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C | 3683.0 | Semi standard non polar | 33892256 | Dihydrodaidzin,3TMS,isomer #6 | C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=C3C(=O)C(C4=CC=C(O)C=C4)COC3=C2)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C | 3691.0 | Semi standard non polar | 33892256 | Dihydrodaidzin,3TMS,isomer #7 | C[Si](C)(C)OC1=CC=C(C2COC3=CC(O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)=CC=C3C2=O)C=C1 | 3741.0 | Semi standard non polar | 33892256 | Dihydrodaidzin,3TMS,isomer #8 | C[Si](C)(C)OC1=CC=C(C2COC3=CC(O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)=CC=C3C2=O)C=C1 | 3742.6 | Semi standard non polar | 33892256 | Dihydrodaidzin,3TMS,isomer #9 | C[Si](C)(C)OC1=CC=C(C2COC3=CC(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=CC=C3C2=O)C=C1 | 3762.6 | Semi standard non polar | 33892256 | Dihydrodaidzin,4TMS,isomer #1 | C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=C3C(=O)C(C4=CC=C(O[Si](C)(C)C)C=C4)COC3=C2)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O | 3700.3 | Semi standard non polar | 33892256 | Dihydrodaidzin,4TMS,isomer #2 | C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=C3C(=O)C(C4=CC=C(O[Si](C)(C)C)C=C4)COC3=C2)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C | 3688.0 | Semi standard non polar | 33892256 | Dihydrodaidzin,4TMS,isomer #3 | C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=C3C(=O)C(C4=CC=C(O[Si](C)(C)C)C=C4)COC3=C2)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C | 3697.8 | Semi standard non polar | 33892256 | Dihydrodaidzin,4TMS,isomer #4 | C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=C3C(=O)C(C4=CC=C(O)C=C4)COC3=C2)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C | 3667.0 | Semi standard non polar | 33892256 | Dihydrodaidzin,4TMS,isomer #5 | C[Si](C)(C)OC1=CC=C(C2COC3=CC(O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=CC=C3C2=O)C=C1 | 3728.6 | Semi standard non polar | 33892256 | Dihydrodaidzin,5TMS,isomer #1 | C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=C3C(=O)C(C4=CC=C(O[Si](C)(C)C)C=C4)COC3=C2)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C | 3682.9 | Semi standard non polar | 33892256 | Dihydrodaidzin,1TBDMS,isomer #1 | CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=C3C(=O)C(C4=CC=C(O)C=C4)COC3=C2)[C@H](O)[C@@H](O)[C@@H]1O | 4068.9 | Semi standard non polar | 33892256 | Dihydrodaidzin,1TBDMS,isomer #2 | CC(C)(C)[Si](C)(C)OC1=CC=C(C2COC3=CC(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)=CC=C3C2=O)C=C1 | 4122.5 | Semi standard non polar | 33892256 | Dihydrodaidzin,1TBDMS,isomer #3 | CC(C)(C)[Si](C)(C)O[C@H]1[C@H](OC2=CC=C3C(=O)C(C4=CC=C(O)C=C4)COC3=C2)O[C@H](CO)[C@@H](O)[C@@H]1O | 4082.5 | Semi standard non polar | 33892256 | Dihydrodaidzin,1TBDMS,isomer #4 | CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](OC2=CC=C3C(=O)C(C4=CC=C(O)C=C4)COC3=C2)O[C@H](CO)[C@H]1O | 4080.4 | Semi standard non polar | 33892256 | Dihydrodaidzin,1TBDMS,isomer #5 | CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](OC2=CC=C3C(=O)C(C4=CC=C(O)C=C4)COC3=C2)[C@H](O)[C@H]1O | 4088.0 | Semi standard non polar | 33892256 | Dihydrodaidzin,2TBDMS,isomer #1 | CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=C3C(=O)C(C4=CC=C(O[Si](C)(C)C(C)(C)C)C=C4)COC3=C2)[C@H](O)[C@@H](O)[C@@H]1O | 4283.1 | Semi standard non polar | 33892256 | Dihydrodaidzin,2TBDMS,isomer #10 | CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](OC2=CC=C3C(=O)C(C4=CC=C(O)C=C4)COC3=C2)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C | 4231.2 | Semi standard non polar | 33892256 | Dihydrodaidzin,2TBDMS,isomer #2 | CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=C3C(=O)C(C4=CC=C(O)C=C4)COC3=C2)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O | 4244.3 | Semi standard non polar | 33892256 | Dihydrodaidzin,2TBDMS,isomer #3 | CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=C3C(=O)C(C4=CC=C(O)C=C4)COC3=C2)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O | 4231.3 | Semi standard non polar | 33892256 | Dihydrodaidzin,2TBDMS,isomer #4 | CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=C3C(=O)C(C4=CC=C(O)C=C4)COC3=C2)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C | 4256.8 | Semi standard non polar | 33892256 | Dihydrodaidzin,2TBDMS,isomer #5 | CC(C)(C)[Si](C)(C)OC1=CC=C(C2COC3=CC(O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]4O)=CC=C3C2=O)C=C1 | 4292.2 | Semi standard non polar | 33892256 | Dihydrodaidzin,2TBDMS,isomer #6 | CC(C)(C)[Si](C)(C)OC1=CC=C(C2COC3=CC(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]4O)=CC=C3C2=O)C=C1 | 4302.0 | Semi standard non polar | 33892256 | Dihydrodaidzin,2TBDMS,isomer #7 | CC(C)(C)[Si](C)(C)OC1=CC=C(C2COC3=CC(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C(C)(C)C)=CC=C3C2=O)C=C1 | 4291.2 | Semi standard non polar | 33892256 | Dihydrodaidzin,2TBDMS,isomer #8 | CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](OC2=CC=C3C(=O)C(C4=CC=C(O)C=C4)COC3=C2)O[C@@H]1CO | 4234.0 | Semi standard non polar | 33892256 | Dihydrodaidzin,2TBDMS,isomer #9 | CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](OC2=CC=C3C(=O)C(C4=CC=C(O)C=C4)COC3=C2)O[C@H](CO)[C@H]1O | 4246.9 | Semi standard non polar | 33892256 | Dihydrodaidzin,3TBDMS,isomer #1 | CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=C3C(=O)C(C4=CC=C(O[Si](C)(C)C(C)(C)C)C=C4)COC3=C2)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O | 4452.7 | Semi standard non polar | 33892256 | Dihydrodaidzin,3TBDMS,isomer #10 | CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](OC2=CC=C3C(=O)C(C4=CC=C(O)C=C4)COC3=C2)O[C@H](CO)[C@H]1O[Si](C)(C)C(C)(C)C | 4320.7 | Semi standard non polar | 33892256 | Dihydrodaidzin,3TBDMS,isomer #2 | CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=C3C(=O)C(C4=CC=C(O[Si](C)(C)C(C)(C)C)C=C4)COC3=C2)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O | 4447.7 | Semi standard non polar | 33892256 | Dihydrodaidzin,3TBDMS,isomer #3 | CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=C3C(=O)C(C4=CC=C(O[Si](C)(C)C(C)(C)C)C=C4)COC3=C2)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C | 4452.6 | Semi standard non polar | 33892256 | Dihydrodaidzin,3TBDMS,isomer #4 | CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=C3C(=O)C(C4=CC=C(O)C=C4)COC3=C2)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O | 4351.1 | Semi standard non polar | 33892256 | Dihydrodaidzin,3TBDMS,isomer #5 | CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=C3C(=O)C(C4=CC=C(O)C=C4)COC3=C2)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C | 4372.1 | Semi standard non polar | 33892256 | Dihydrodaidzin,3TBDMS,isomer #6 | CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=C3C(=O)C(C4=CC=C(O)C=C4)COC3=C2)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C | 4347.7 | Semi standard non polar | 33892256 | Dihydrodaidzin,3TBDMS,isomer #7 | CC(C)(C)[Si](C)(C)OC1=CC=C(C2COC3=CC(O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]4O)=CC=C3C2=O)C=C1 | 4430.6 | Semi standard non polar | 33892256 | Dihydrodaidzin,3TBDMS,isomer #8 | CC(C)(C)[Si](C)(C)OC1=CC=C(C2COC3=CC(O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C(C)(C)C)=CC=C3C2=O)C=C1 | 4438.8 | Semi standard non polar | 33892256 | Dihydrodaidzin,3TBDMS,isomer #9 | CC(C)(C)[Si](C)(C)OC1=CC=C(C2COC3=CC(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]4O[Si](C)(C)C(C)(C)C)=CC=C3C2=O)C=C1 | 4450.4 | Semi standard non polar | 33892256 | Dihydrodaidzin,4TBDMS,isomer #1 | CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=C3C(=O)C(C4=CC=C(O[Si](C)(C)C(C)(C)C)C=C4)COC3=C2)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O | 4537.6 | Semi standard non polar | 33892256 | Dihydrodaidzin,4TBDMS,isomer #2 | CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=C3C(=O)C(C4=CC=C(O[Si](C)(C)C(C)(C)C)C=C4)COC3=C2)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C | 4560.4 | Semi standard non polar | 33892256 | Dihydrodaidzin,4TBDMS,isomer #3 | CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=C3C(=O)C(C4=CC=C(O[Si](C)(C)C(C)(C)C)C=C4)COC3=C2)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C | 4528.5 | Semi standard non polar | 33892256 | Dihydrodaidzin,4TBDMS,isomer #4 | CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC=C3C(=O)C(C4=CC=C(O)C=C4)COC3=C2)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C | 4478.6 | Semi standard non polar | 33892256 | Dihydrodaidzin,4TBDMS,isomer #5 | CC(C)(C)[Si](C)(C)OC1=CC=C(C2COC3=CC(O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]4O[Si](C)(C)C(C)(C)C)=CC=C3C2=O)C=C1 | 4506.3 | Semi standard non polar | 33892256 |
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