| Record Information |
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| Version | 2.0 |
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| Created at | 2022-02-14 20:40:14 UTC |
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| Updated at | 2022-03-10 22:16:36 UTC |
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| NP-MRD ID | NP0044261 |
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| Secondary Accession Numbers | None |
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| Natural Product Identification |
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| Common Name | (S)-2,3-Epoxysqualene |
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| Description | (S)-2,3-Epoxysqualene, also known as 2,3-oxidosqualene or (S)-squalene-2,3-epoxide, belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. Thus, (S)-2,3-epoxysqualene is considered to be an isoprenoid lipid molecule (S)-2,3-Epoxysqualene is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral. (S)-2,3-Epoxysqualene is expected to be in Cannabis as all living plants are known to produce and metabolize it. |
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| Structure | CC(C)=CCC\C(C)=C\CC\C(C)=C\CC\C=C(/C)CC\C=C(/C)CC[C@@H]1OC1(C)C InChI=1S/C30H50O/c1-24(2)14-11-17-27(5)20-12-18-25(3)15-9-10-16-26(4)19-13-21-28(6)22-23-29-30(7,8)31-29/h14-16,20-21,29H,9-13,17-19,22-23H2,1-8H3/b25-15+,26-16+,27-20+,28-21+/t29-/m0/s1 |
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| Synonyms | | Value | Source |
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| (3S)-2,3-Dihydro-2,3-epoxysqualene | ChEBI | | (3S)-2,3-Epoxy-2,3-dihydrosqualene | ChEBI | | (S)-2,3-Dihydro-2,3-epoxysqualene | ChEBI | | (S)-2,3-Epoxy-2,3-dihydrosqualene | ChEBI | | (S)-2,3-Oxidosqualene | ChEBI | | (S)-Squalene-2,3-epoxide | ChEBI | | 2,3-EDSQ | ChEBI | | 2,3-Epoxisqualene | ChEBI | | 2,3-Oxidosqualene | ChEBI | | Oxidosqualene | ChEBI | | Squalene 2,3-epoxide | ChEBI | | Squalene 2,3-oxide | ChEBI | | 2,3-Epoxy-2,3-dihydrosqualene | HMDB | | 2,3-Oxidosqualene, (R)-isomer | HMDB | | 2,3-Oxidosqualene, (R-(all-e))-isomer | HMDB | | 2,3-Oxidosqualene, (all-e)-(+-)-isomer | HMDB | | Squalene monohydroperoxide | HMDB | | Squalene-2,3-epoxide | HMDB | | (3S)-Oxidosqualene | HMDB | | 2,3-Oxidosqualene, (S-(all-e))-isomer | HMDB | | Squalene-2,3-oxide | HMDB | | 2,3-Oxidosqualene, (S)-isomer | HMDB | | Squslene oxide | HMDB | | Squalene peroxide | HMDB | | (3S)-2,3-Epoxysqualene | HMDB | | (3S)-2,3-Oxidosqualene | HMDB | | (3S)-Squalene-2,3-epoxide | HMDB | | (S)-Squalene 2,3-epoxide | HMDB | | 2,3(S)-Oxidosqualene | HMDB | | 3(S)-Oxidosqualene | HMDB | | Squalene 2,3(S)-oxide | HMDB | | (3R,S)-Oxidosqualene | HMDB | | (R,S)-Squalene 2,3-epoxide | HMDB | | (RS)-2,3-Epoxy-2,3-dihydrosqualene | HMDB | | (±)-2,3-epoxysqualene | HMDB | | (±)-squalene oxide | HMDB | | 2,3-Epoxysqualene | HMDB | | Squalene epoxide | HMDB | | Squalene oxide | HMDB | | (3S)-2,2-Dimethyl-3-[(3E,7E,11E,15E)-3,7,12,16,20-pentamethyl-3,7,11,15,19-heneicosapentaen-1-yl]oxirane | HMDB | | (S)-2,3-Epoxysqualene | HMDB |
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| Chemical Formula | C30H50O |
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| Average Mass | 426.7174 Da |
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| Monoisotopic Mass | 426.38617 Da |
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| IUPAC Name | (3S)-2,2-dimethyl-3-[(3E,7E,11E,15E)-3,7,12,16,20-pentamethylhenicosa-3,7,11,15,19-pentaen-1-yl]oxirane |
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| Traditional Name | squalene 2,3-oxide |
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| CAS Registry Number | 54910-48-4 |
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| SMILES | CC(C)=CCC\C(C)=C\CC\C(C)=C\CC\C=C(/C)CC\C=C(/C)CC[C@@H]1OC1(C)C |
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| InChI Identifier | InChI=1S/C30H50O/c1-24(2)14-11-17-27(5)20-12-18-25(3)15-9-10-16-26(4)19-13-21-28(6)22-23-29-30(7,8)31-29/h14-16,20-21,29H,9-13,17-19,22-23H2,1-8H3/b25-15+,26-16+,27-20+,28-21+/t29-/m0/s1 |
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| InChI Key | QYIMSPSDBYKPPY-RSKUXYSASA-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, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | | 1D NMR | 1H NMR Spectrum (1D, 100 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | | 1D NMR | 13C NMR Spectrum (1D, 252 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | | 1D NMR | 1H NMR Spectrum (1D, 1000 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | | 1D NMR | 13C NMR Spectrum (1D, 50 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | | 1D NMR | 1H NMR Spectrum (1D, 200 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | | 1D NMR | 13C NMR Spectrum (1D, 75 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | | 1D NMR | 1H NMR Spectrum (1D, 300 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | | 1D NMR | 13C NMR Spectrum (1D, 101 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | | 1D NMR | 1H NMR Spectrum (1D, 400 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | | 1D NMR | 13C NMR Spectrum (1D, 126 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | | 1D NMR | 1H NMR Spectrum (1D, 500 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | | 1D NMR | 13C NMR Spectrum (1D, 151 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | | 1D NMR | 1H NMR Spectrum (1D, 600 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | | 1D NMR | 13C NMR Spectrum (1D, 176 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | | 1D NMR | 1H NMR Spectrum (1D, 700 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | | 1D NMR | 13C NMR Spectrum (1D, 201 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | | 1D NMR | 1H NMR Spectrum (1D, 800 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | | 1D NMR | 13C NMR Spectrum (1D, 226 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | | 1D NMR | 1H NMR Spectrum (1D, 900 MHz, D2O, 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 triterpenoids. These are terpene molecules containing six isoprene units. |
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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 | Triterpenoids |
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| Direct Parent | Triterpenoids |
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| Alternative Parents | |
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| Substituents | - Triterpenoid
- Oxacycle
- Organoheterocyclic compound
- Ether
- Oxirane
- Dialkyl ether
- Organic oxygen compound
- Hydrocarbon derivative
- Organooxygen compound
- Aliphatic heteromonocyclic compound
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| Molecular Framework | Aliphatic heteromonocyclic compounds |
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| External Descriptors | |
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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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