Record Information |
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Version | 1.0 |
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Created at | 2022-09-09 22:15:47 UTC |
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Updated at | 2022-09-09 22:15:47 UTC |
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NP-MRD ID | NP0291245 |
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Secondary Accession Numbers | None |
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Natural Product Identification |
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Common Name | (4s,5as,7s,9as)-4-hydroxy-7,9a-dimethyl-6-methylidene-3h,4h,5h,5ah,7h,8h,9h-naphtho[1,2-c]furan-1-one |
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Description | 7Beta-Hydroxy-4(13),8-coloratadien-11,12-olide belongs to the class of organic compounds known as terpene lactones. These are prenol lipids containing a lactone ring. (4s,5as,7s,9as)-4-hydroxy-7,9a-dimethyl-6-methylidene-3h,4h,5h,5ah,7h,8h,9h-naphtho[1,2-c]furan-1-one is found in Warburgia ugandensis. It was first documented in 2005 (PMID: 16153670). Based on a literature review very few articles have been published on 7beta-Hydroxy-4(13),8-coloratadien-11,12-olide. |
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Structure | C[C@H]1CC[C@@]2(C)[C@@H](C[C@H](O)C3=C2C(=O)OC3)C1=C InChI=1S/C15H20O3/c1-8-4-5-15(3)11(9(8)2)6-12(16)10-7-18-14(17)13(10)15/h8,11-12,16H,2,4-7H2,1,3H3/t8-,11-,12-,15-/m0/s1 |
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Synonyms | Value | Source |
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7b-Hydroxy-4(13),8-coloratadien-11,12-olide | Generator | 7Β-hydroxy-4(13),8-coloratadien-11,12-olide | Generator |
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Chemical Formula | C15H20O3 |
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Average Mass | 248.3220 Da |
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Monoisotopic Mass | 248.14124 Da |
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IUPAC Name | (4S,5aS,7S,9aS)-4-hydroxy-7,9a-dimethyl-6-methylidene-1H,3H,4H,5H,5aH,6H,7H,8H,9H,9aH-naphtho[1,2-c]furan-1-one |
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Traditional Name | (4S,5aS,7S,9aS)-4-hydroxy-7,9a-dimethyl-6-methylidene-3H,4H,5H,5aH,7H,8H,9H-naphtho[1,2-c]furan-1-one |
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CAS Registry Number | Not Available |
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SMILES | C[C@H]1CC[C@@]2(C)[C@@H](C[C@H](O)C3=C2C(=O)OC3)C1=C |
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InChI Identifier | InChI=1S/C15H20O3/c1-8-4-5-15(3)11(9(8)2)6-12(16)10-7-18-14(17)13(10)15/h8,11-12,16H,2,4-7H2,1,3H3/t8-,11-,12-,15-/m0/s1 |
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InChI Key | YIADAXTULGQCOZ-REXDEQPNSA-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 | |
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Chemical Taxonomy |
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Description | Belongs to the class of organic compounds known as terpene lactones. These are prenol lipids containing a lactone ring. |
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Kingdom | Organic compounds |
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Super Class | Lipids and lipid-like molecules |
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Class | Prenol lipids |
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Sub Class | Terpene lactones |
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Direct Parent | Terpene lactones |
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Alternative Parents | |
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Substituents | - Terpene lactone
- Sesquiterpenoid
- Naphthofuran
- 2-furanone
- Dihydrofuran
- Alpha,beta-unsaturated carboxylic ester
- Enoate ester
- Carboxylic acid ester
- Lactone
- Secondary alcohol
- Monocarboxylic acid or derivatives
- Carboxylic acid derivative
- Oxacycle
- Organoheterocyclic compound
- Organooxygen compound
- Hydrocarbon derivative
- Organic oxide
- Alcohol
- Carbonyl group
- Organic oxygen compound
- Aliphatic heteropolycyclic compound
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Molecular Framework | Aliphatic 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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