Record Information |
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Version | 1.0 |
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Created at | 2022-04-28 11:51:59 UTC |
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Updated at | 2022-04-28 11:51:59 UTC |
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NP-MRD ID | NP0067298 |
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Secondary Accession Numbers | None |
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Natural Product Identification |
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Common Name | Ternatine |
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Description | (1S,5R,6R,8R,9S,11R,13R,14S,15S,16R,17S,18S,19R)-6,13,19-trihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.0¹,⁸.0⁵,¹⁷.0⁷,¹⁶.0⁹,¹⁴.0¹⁴,¹⁸]Nonadecan-15-yl 2-methylpropanoate belongs to the class of organic compounds known as hetisine-type diterpenoid alkaloids. These are alkaloid diterpenoids with a structure based on the hetisine skeleton, which is a heptacyclic compound with an additional N-C-6 bond as compared with the hetidine-type, and thus, is one of most complex entries in the atisane-class. Ternatine is found in Delphinium ternatum. Based on a literature review very few articles have been published on (1S,5R,6R,8R,9S,11R,13R,14S,15S,16R,17S,18S,19R)-6,13,19-trihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.0¹,⁸.0⁵,¹⁷.0⁷,¹⁶.0⁹,¹⁴.0¹⁴,¹⁸]Nonadecan-15-yl 2-methylpropanoate. |
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Structure | CC(C)C(=O)O[C@@H]1[C@H]2[C@@H]3[C@@]4(C)CCC[C@]33[C@@H]([C@H]5C[C@H]6[C@@H](O)[C@@H]3[C@@]15[C@H](O)C6=C)N2[C@@H]4O InChI=1S/C24H33NO5/c1-9(2)20(28)30-19-13-15-22(4)6-5-7-23(15)16-14(26)11-8-12(17(23)25(13)21(22)29)24(16,19)18(27)10(11)3/h9,11-19,21,26-27,29H,3,5-8H2,1-2,4H3/t11-,12-,13-,14-,15-,16+,17-,18-,19-,21-,22-,23+,24+/m1/s1 |
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Synonyms | Value | Source |
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(1S,5R,6R,8R,9S,11R,13R,14S,15S,16R,17S,18S,19R)-6,13,19-Trihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.0,.0,.0,.0,.0,]nonadecan-15-yl 2-methylpropanoic acid | Generator |
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Chemical Formula | C24H33NO5 |
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Average Mass | 415.5300 Da |
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Monoisotopic Mass | 415.23587 Da |
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IUPAC Name | (1S,5R,6R,8R,9S,11R,13R,14S,15S,16R,17S,18S,19R)-6,13,19-trihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.0^{1,8}.0^{5,17}.0^{7,16}.0^{9,14}.0^{14,18}]nonadecan-15-yl 2-methylpropanoate |
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Traditional Name | (1S,5R,6R,8R,9S,11R,13R,14S,15S,16R,17S,18S,19R)-6,13,19-trihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.0^{1,8}.0^{5,17}.0^{7,16}.0^{9,14}.0^{14,18}]nonadecan-15-yl 2-methylpropanoate |
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CAS Registry Number | Not Available |
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SMILES | CC(C)C(=O)O[C@@H]1[C@H]2[C@@H]3[C@@]4(C)CCC[C@]33[C@@H]([C@H]5C[C@H]6[C@@H](O)[C@@H]3[C@@]15[C@H](O)C6=C)N2[C@@H]4O |
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InChI Identifier | InChI=1S/C24H33NO5/c1-9(2)20(28)30-19-13-15-22(4)6-5-7-23(15)16-14(26)11-8-12(17(23)25(13)21(22)29)24(16,19)18(27)10(11)3/h9,11-19,21,26-27,29H,3,5-8H2,1-2,4H3/t11-,12-,13-,14-,15-,16+,17-,18-,19-,21-,22-,23+,24+/m1/s1 |
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InChI Key | JAONFTKYPDCXJH-SSZYRXBQSA-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 hetisine-type diterpenoid alkaloids. These are alkaloid diterpenoids with a structure based on the hetisine skeleton, which is a heptacyclic compound with an additional N-C-6 bond as compared with the hetidine-type, and thus, is one of most complex entries in the atisane-class. |
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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 | Diterpenoids |
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Direct Parent | Hetisine-type diterpenoid alkaloids |
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Alternative Parents | |
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Substituents | - Hetisine-type diterpenoid alkaloid
- Quinolizidine
- Azaspirodecane
- Alkaloid or derivatives
- Isoindole or derivatives
- Isoindoline
- Indolizidine
- Indole or derivatives
- Azepane
- N-alkylpyrrolidine
- Piperidine
- Pyrrolidine
- Cyclic alcohol
- Secondary alcohol
- Hemiaminal
- Carboxylic acid ester
- Azacycle
- Organoheterocyclic compound
- Polyol
- Monocarboxylic acid or derivatives
- Carboxylic acid derivative
- Alkanolamine
- Organic nitrogen compound
- Organic oxygen compound
- Organopnictogen compound
- Organic oxide
- Hydrocarbon derivative
- Organooxygen compound
- Organonitrogen compound
- Carbonyl group
- Alcohol
- 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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