Record Information |
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Version | 1.0 |
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Created at | 2022-09-11 04:43:29 UTC |
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Updated at | 2022-09-11 04:43:29 UTC |
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NP-MRD ID | NP0309849 |
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Secondary Accession Numbers | None |
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Natural Product Identification |
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Common Name | (3s,3'r,3ar,6s,6ar)-3a-{[(2s,3r,4r,5s,6r)-5-(acetyloxy)-6-[(acetyloxy)methyl]-3,4-dihydroxyoxan-2-yl]oxy}-3'-(4-hydroxyphenyl)-2,5'-dioxo-dihydro-5h-spiro[furo[3,2-b]furan-3,2'-oxolan]-6-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate |
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Description | (3S,3'R,3aR,6S,6aR)-3a-{[(2S,3R,4R,5S,6R)-5-(acetyloxy)-6-[(acetyloxy)methyl]-3,4-dihydroxyoxan-2-yl]oxy}-3'-(4-hydroxyphenyl)-2,5'-dioxo-tetrahydro-2H-spiro[furo[3,2-b]furan-3,2'-oxolane]-6-yl (2E)-3-(4-hydroxyphenyl)prop-2-enoate belongs to the class of organic compounds known as pentacarboxylic acids and derivatives. These are carboxylic acids containing exactly five carboxyl groups. Based on a literature review very few articles have been published on (3S,3'R,3aR,6S,6aR)-3a-{[(2S,3R,4R,5S,6R)-5-(acetyloxy)-6-[(acetyloxy)methyl]-3,4-dihydroxyoxan-2-yl]oxy}-3'-(4-hydroxyphenyl)-2,5'-dioxo-tetrahydro-2H-spiro[furo[3,2-b]furan-3,2'-oxolane]-6-yl (2E)-3-(4-hydroxyphenyl)prop-2-enoate. |
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Structure | CC(=O)OC[C@H]1O[C@@H](O[C@]23OC[C@H](OC(=O)\C=C\C4=CC=C(O)C=C4)[C@H]2OC(=O)[C@@]32OC(=O)C[C@@H]2C2=CC=C(O)C=C2)[C@H](O)[C@@H](O)[C@@H]1OC(C)=O InChI=1S/C34H34O17/c1-16(35)44-14-23-29(46-17(2)36)27(41)28(42)31(48-23)51-34-30(24(15-45-34)47-25(39)12-5-18-3-8-20(37)9-4-18)49-32(43)33(34)22(13-26(40)50-33)19-6-10-21(38)11-7-19/h3-12,22-24,27-31,37-38,41-42H,13-15H2,1-2H3/b12-5+/t22-,23-,24+,27-,28-,29-,30-,31+,33-,34-/m1/s1 |
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Synonyms | Value | Source |
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(3S,3'r,3AR,6S,6ar)-3a-{[(2S,3R,4R,5S,6R)-5-(acetyloxy)-6-[(acetyloxy)methyl]-3,4-dihydroxyoxan-2-yl]oxy}-3'-(4-hydroxyphenyl)-2,5'-dioxo-tetrahydro-2H-spiro[furo[3,2-b]furan-3,2'-oxolane]-6-yl (2E)-3-(4-hydroxyphenyl)prop-2-enoic acid | Generator |
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Chemical Formula | C34H34O17 |
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Average Mass | 714.6290 Da |
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Monoisotopic Mass | 714.17960 Da |
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IUPAC Name | (3S,3'R,3aR,6S,6aR)-3a-{[(2S,3R,4R,5S,6R)-5-(acetyloxy)-6-[(acetyloxy)methyl]-3,4-dihydroxyoxan-2-yl]oxy}-3'-(4-hydroxyphenyl)-2,5'-dioxo-tetrahydro-2H-spiro[furo[3,2-b]furan-3,2'-oxolane]-6-yl (2E)-3-(4-hydroxyphenyl)prop-2-enoate |
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Traditional Name | (3S,3'R,3aR,6S,6aR)-3a-{[(2S,3R,4R,5S,6R)-5-(acetyloxy)-6-[(acetyloxy)methyl]-3,4-dihydroxyoxan-2-yl]oxy}-3'-(4-hydroxyphenyl)-2,5'-dioxo-dihydro-5H-spiro[furo[3,2-b]furan-3,2'-oxolane]-6-yl (2E)-3-(4-hydroxyphenyl)prop-2-enoate |
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CAS Registry Number | Not Available |
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SMILES | CC(=O)OC[C@H]1O[C@@H](O[C@]23OC[C@H](OC(=O)\C=C\C4=CC=C(O)C=C4)[C@H]2OC(=O)[C@@]32OC(=O)C[C@@H]2C2=CC=C(O)C=C2)[C@H](O)[C@@H](O)[C@@H]1OC(C)=O |
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InChI Identifier | InChI=1S/C34H34O17/c1-16(35)44-14-23-29(46-17(2)36)27(41)28(42)31(48-23)51-34-30(24(15-45-34)47-25(39)12-5-18-3-8-20(37)9-4-18)49-32(43)33(34)22(13-26(40)50-33)19-6-10-21(38)11-7-19/h3-12,22-24,27-31,37-38,41-42H,13-15H2,1-2H3/b12-5+/t22-,23-,24+,27-,28-,29-,30-,31+,33-,34-/m1/s1 |
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InChI Key | VZJTUABWBMICNX-KMUMPUDJSA-N |
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Experimental Spectra |
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| Not Available | Predicted Spectra |
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| Spectrum Type | Description | Depositor ID | Depositor Organization | Depositor | Deposition Date | View |
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1D NMR | 13C NMR Spectrum (1D, 25 MHz, H2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 1H NMR Spectrum (1D, 100 MHz, H2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 13C NMR Spectrum (1D, 252 MHz, H2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 1H NMR Spectrum (1D, 1000 MHz, H2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 13C NMR Spectrum (1D, 50 MHz, H2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 1H NMR Spectrum (1D, 200 MHz, H2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 13C NMR Spectrum (1D, 75 MHz, H2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 1H NMR Spectrum (1D, 300 MHz, H2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 13C NMR Spectrum (1D, 101 MHz, H2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 1H NMR Spectrum (1D, 400 MHz, H2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 13C NMR Spectrum (1D, 126 MHz, H2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 1H NMR Spectrum (1D, 500 MHz, H2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 13C NMR Spectrum (1D, 151 MHz, H2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 1H NMR Spectrum (1D, 600 MHz, H2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 13C NMR Spectrum (1D, 176 MHz, H2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 1H NMR Spectrum (1D, 700 MHz, H2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 13C NMR Spectrum (1D, 201 MHz, H2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 1H NMR Spectrum (1D, 800 MHz, H2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 13C NMR Spectrum (1D, 226 MHz, H2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 1H NMR Spectrum (1D, 900 MHz, H2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum |
| Chemical Shift Submissions |
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| Not Available | Species |
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Species of Origin | Not Available |
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Chemical Taxonomy |
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Description | Belongs to the class of organic compounds known as pentacarboxylic acids and derivatives. These are carboxylic acids containing exactly five carboxyl groups. |
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Kingdom | Organic compounds |
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Super Class | Organic acids and derivatives |
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Class | Carboxylic acids and derivatives |
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Sub Class | Pentacarboxylic acids and derivatives |
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Direct Parent | Pentacarboxylic acids and derivatives |
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Alternative Parents | |
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Substituents | - Pentacarboxylic acid or derivatives
- Coumaric acid ester
- Hydroxycinnamic acid or derivatives
- Cinnamic acid or derivatives
- Coumaric acid or derivatives
- Cinnamic acid ester
- O-glycosyl compound
- Disaccharide
- Glycosyl compound
- Isosorbide
- Styrene
- Furofuran
- 1-hydroxy-2-unsubstituted benzenoid
- Phenol
- Ketal
- Fatty acid ester
- Gamma butyrolactone
- Benzenoid
- Fatty acyl
- Oxane
- Monocyclic benzene moiety
- Alpha,beta-unsaturated carboxylic ester
- Enoate ester
- Tetrahydrofuran
- 1,2-diol
- Carboxylic acid ester
- Secondary alcohol
- Lactone
- Acetal
- Organoheterocyclic compound
- Oxacycle
- Alcohol
- Hydrocarbon derivative
- Organic oxide
- Carbonyl group
- Organic oxygen compound
- 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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Physical Properties |
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State | Not Available |
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Experimental 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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Predicted Properties | |
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