Record Information |
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Version | 1.0 |
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Created at | 2022-09-07 21:11:12 UTC |
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Updated at | 2022-09-07 21:11:12 UTC |
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NP-MRD ID | NP0256380 |
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Secondary Accession Numbers | None |
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Natural Product Identification |
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Common Name | (1r,6s,10s,11s,12s,15s)-6,12,16-trimethyl-2-methylidenetricyclo[7.5.2.0¹²,¹⁵]hexadec-9(16)-ene-10,11-diol |
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Description | (1R,6S,10S,11S,12S,15S)-6,12,16-trimethyl-2-methylidenetricyclo[7.5.2.0¹²,¹⁵]Hexadec-9(16)-ene-10,11-diol belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. (1r,6s,10s,11s,12s,15s)-6,12,16-trimethyl-2-methylidenetricyclo[7.5.2.0¹²,¹⁵]hexadec-9(16)-ene-10,11-diol is found in Nasutitermes costalis and Nasutitermes nigriceps. Based on a literature review very few articles have been published on (1R,6S,10S,11S,12S,15S)-6,12,16-trimethyl-2-methylidenetricyclo[7.5.2.0¹²,¹⁵]Hexadec-9(16)-ene-10,11-diol. |
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Structure | C[C@H]1CCCC(=C)[C@@H]2CC[C@@]3(C)[C@@H]2C(C)=C(CC1)[C@H](O)[C@H]3O InChI=1S/C20H32O2/c1-12-6-5-7-13(2)15-10-11-20(4)17(15)14(3)16(9-8-12)18(21)19(20)22/h12,15,17-19,21-22H,2,5-11H2,1,3-4H3/t12-,15-,17+,18-,19+,20-/m0/s1 |
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Synonyms | Not Available |
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Chemical Formula | C20H32O2 |
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Average Mass | 304.4740 Da |
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Monoisotopic Mass | 304.24023 Da |
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IUPAC Name | (1R,6S,10S,11S,12S,15S)-6,12,16-trimethyl-2-methylidenetricyclo[7.5.2.0^{12,15}]hexadec-9(16)-ene-10,11-diol |
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Traditional Name | (1R,6S,10S,11S,12S,15S)-6,12,16-trimethyl-2-methylidenetricyclo[7.5.2.0^{12,15}]hexadec-9(16)-ene-10,11-diol |
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CAS Registry Number | Not Available |
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SMILES | C[C@H]1CCCC(=C)[C@@H]2CC[C@@]3(C)[C@@H]2C(C)=C(CC1)[C@H](O)[C@H]3O |
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InChI Identifier | InChI=1S/C20H32O2/c1-12-6-5-7-13(2)15-10-11-20(4)17(15)14(3)16(9-8-12)18(21)19(20)22/h12,15,17-19,21-22H,2,5-11H2,1,3-4H3/t12-,15-,17+,18-,19+,20-/m0/s1 |
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InChI Key | KKUYFJMPBSOTQV-NJSRCQLFSA-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 diterpenoids. These are terpene compounds formed by four 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 | Diterpenoids |
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Direct Parent | Diterpenoids |
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Alternative Parents | |
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Substituents | - Trinervitane or kempane diterpenoid
- Diterpenoid
- Secondary alcohol
- 1,2-diol
- Organic oxygen compound
- Hydrocarbon derivative
- Organooxygen compound
- Alcohol
- Aliphatic homopolycyclic compound
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Molecular Framework | Aliphatic homopolycyclic 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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