Record Information |
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Version | 5.0 |
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Status | Expected but not Quantified |
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Creation Date | 2012-09-11 20:51:58 UTC |
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Update Date | 2022-03-07 02:54:39 UTC |
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HMDB ID | HMDB0035843 |
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Secondary Accession Numbers | |
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Metabolite Identification |
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Common Name | (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione |
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Description | (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione is an extremely weak basic (essentially neutral) compound (based on its pKa). |
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Structure | CCC(O)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC23C)C2(C)CCC(=O)C(C)(CO)C2CC4)O1 InChI=1S/C29H44O5/c1-7-20(31)21-14-17(2)29(34-21)15-24(33)28(6)19-8-9-22-25(3,18(19)10-13-27(28,29)5)12-11-23(32)26(22,4)16-30/h17,20-22,30-31H,7-16H2,1-6H3 |
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Synonyms | Not Available |
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Chemical Formula | C29H44O5 |
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Average Molecular Weight | 472.6567 |
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Monoisotopic Molecular Weight | 472.318874518 |
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IUPAC Name | 6'-(hydroxymethyl)-5-(1-hydroxypropyl)-2',3,6',11',15'-pentamethylspiro[oxolane-2,14'-tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan]-1'(10')-ene-5',12'-dione |
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Traditional Name | 6'-(hydroxymethyl)-5-(1-hydroxypropyl)-2',3,6',11',15'-pentamethylspiro[oxolane-2,14'-tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan]-1'(10')-ene-5',12'-dione |
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CAS Registry Number | Not Available |
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SMILES | CCC(O)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC23C)C2(C)CCC(=O)C(C)(CO)C2CC4)O1 |
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InChI Identifier | InChI=1S/C29H44O5/c1-7-20(31)21-14-17(2)29(34-21)15-24(33)28(6)19-8-9-22-25(3,18(19)10-13-27(28,29)5)12-11-23(32)26(22,4)16-30/h17,20-22,30-31H,7-16H2,1-6H3 |
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InChI Key | IPZHIWYVRSTEKX-UHFFFAOYSA-N |
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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 | Not Available |
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Substituents | Not Available |
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Molecular Framework | Aliphatic heteropolycyclic compounds |
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External Descriptors | Not Available |
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Ontology |
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Physiological effect | Not Available |
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Disposition | |
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Process | |
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Role | |
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Physical Properties |
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State | Solid |
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Experimental Molecular Properties | Property | Value | Reference |
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Melting Point | 194 - 195 °C | Not Available | Boiling Point | Not Available | Not Available | Water Solubility | Not Available | Not Available | LogP | Not Available | Not Available |
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Experimental Chromatographic Properties | Not Available |
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Predicted Molecular Properties | |
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Predicted Chromatographic Properties | Predicted Collision Cross SectionsPredicted Kovats Retention IndicesUnderivatizedMetabolite | SMILES | Kovats RI Value | Column Type | Reference |
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(23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione | CCC(O)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC23C)C2(C)CCC(=O)C(C)(CO)C2CC4)O1 | 3292.1 | Standard polar | 33892256 | (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione | CCC(O)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC23C)C2(C)CCC(=O)C(C)(CO)C2CC4)O1 | 3659.3 | Standard non polar | 33892256 | (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione | CCC(O)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC23C)C2(C)CCC(=O)C(C)(CO)C2CC4)O1 | 3975.0 | Semi standard non polar | 33892256 |
DerivatizedDerivative Name / Structure | SMILES | Kovats RI Value | Column Type | Reference |
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(23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione,1TMS,isomer #1 | CCC(O[Si](C)(C)C)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CCC(=O)C(C)(CO)C2CC4)O1 | 3750.5 | Semi standard non polar | 33892256 | (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione,1TMS,isomer #2 | CCC(O)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CCC(=O)C(C)(CO[Si](C)(C)C)C2CC4)O1 | 3677.4 | Semi standard non polar | 33892256 | (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione,1TMS,isomer #3 | CCC(O)C1CC(C)C2(C=C(O[Si](C)(C)C)C3(C)C4=C(CCC32C)C2(C)CCC(=O)C(C)(CO)C2CC4)O1 | 3620.1 | Semi standard non polar | 33892256 | (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione,1TMS,isomer #4 | CCC(O)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C)C(C)(CO)C2CC4)O1 | 3675.8 | Semi standard non polar | 33892256 | (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione,2TMS,isomer #1 | CCC(O[Si](C)(C)C)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CCC(=O)C(C)(CO[Si](C)(C)C)C2CC4)O1 | 3678.4 | Semi standard non polar | 33892256 | (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione,2TMS,isomer #2 | CCC(O[Si](C)(C)C)C1CC(C)C2(C=C(O[Si](C)(C)C)C3(C)C4=C(CCC32C)C2(C)CCC(=O)C(C)(CO)C2CC4)O1 | 3617.0 | Semi standard non polar | 33892256 | (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione,2TMS,isomer #3 | CCC(O[Si](C)(C)C)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C)C(C)(CO)C2CC4)O1 | 3671.8 | Semi standard non polar | 33892256 | (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione,2TMS,isomer #4 | CCC(O)C1CC(C)C2(C=C(O[Si](C)(C)C)C3(C)C4=C(CCC32C)C2(C)CCC(=O)C(C)(CO[Si](C)(C)C)C2CC4)O1 | 3545.2 | Semi standard non polar | 33892256 | (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione,2TMS,isomer #5 | CCC(O)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C)C(C)(CO[Si](C)(C)C)C2CC4)O1 | 3616.1 | Semi standard non polar | 33892256 | (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione,2TMS,isomer #6 | CCC(O)C1CC(C)C2(C=C(O[Si](C)(C)C)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C)C(C)(CO)C2CC4)O1 | 3530.2 | Semi standard non polar | 33892256 | (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione,3TMS,isomer #1 | CCC(O[Si](C)(C)C)C1CC(C)C2(C=C(O[Si](C)(C)C)C3(C)C4=C(CCC32C)C2(C)CCC(=O)C(C)(CO[Si](C)(C)C)C2CC4)O1 | 3552.2 | Semi standard non polar | 33892256 | (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione,3TMS,isomer #1 | CCC(O[Si](C)(C)C)C1CC(C)C2(C=C(O[Si](C)(C)C)C3(C)C4=C(CCC32C)C2(C)CCC(=O)C(C)(CO[Si](C)(C)C)C2CC4)O1 | 3592.1 | Standard non polar | 33892256 | (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione,3TMS,isomer #2 | CCC(O[Si](C)(C)C)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C)C(C)(CO[Si](C)(C)C)C2CC4)O1 | 3623.6 | Semi standard non polar | 33892256 | (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione,3TMS,isomer #2 | CCC(O[Si](C)(C)C)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C)C(C)(CO[Si](C)(C)C)C2CC4)O1 | 3551.8 | Standard non polar | 33892256 | (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione,3TMS,isomer #3 | CCC(O[Si](C)(C)C)C1CC(C)C2(C=C(O[Si](C)(C)C)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C)C(C)(CO)C2CC4)O1 | 3533.1 | Semi standard non polar | 33892256 | (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione,3TMS,isomer #3 | CCC(O[Si](C)(C)C)C1CC(C)C2(C=C(O[Si](C)(C)C)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C)C(C)(CO)C2CC4)O1 | 3483.9 | Standard non polar | 33892256 | (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione,3TMS,isomer #4 | CCC(O)C1CC(C)C2(C=C(O[Si](C)(C)C)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C)C(C)(CO[Si](C)(C)C)C2CC4)O1 | 3495.5 | Semi standard non polar | 33892256 | (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione,3TMS,isomer #4 | CCC(O)C1CC(C)C2(C=C(O[Si](C)(C)C)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C)C(C)(CO[Si](C)(C)C)C2CC4)O1 | 3482.6 | Standard non polar | 33892256 | (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione,4TMS,isomer #1 | CCC(O[Si](C)(C)C)C1CC(C)C2(C=C(O[Si](C)(C)C)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C)C(C)(CO[Si](C)(C)C)C2CC4)O1 | 3487.8 | Semi standard non polar | 33892256 | (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione,4TMS,isomer #1 | CCC(O[Si](C)(C)C)C1CC(C)C2(C=C(O[Si](C)(C)C)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C)C(C)(CO[Si](C)(C)C)C2CC4)O1 | 3497.4 | Standard non polar | 33892256 | (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione,1TBDMS,isomer #1 | CCC(O[Si](C)(C)C(C)(C)C)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CCC(=O)C(C)(CO)C2CC4)O1 | 3991.6 | Semi standard non polar | 33892256 | (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione,1TBDMS,isomer #2 | CCC(O)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CCC(=O)C(C)(CO[Si](C)(C)C(C)(C)C)C2CC4)O1 | 3925.0 | Semi standard non polar | 33892256 | (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione,1TBDMS,isomer #3 | CCC(O)C1CC(C)C2(C=C(O[Si](C)(C)C(C)(C)C)C3(C)C4=C(CCC32C)C2(C)CCC(=O)C(C)(CO)C2CC4)O1 | 3870.3 | Semi standard non polar | 33892256 | (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione,1TBDMS,isomer #4 | CCC(O)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(CO)C2CC4)O1 | 3914.4 | Semi standard non polar | 33892256 | (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione,2TBDMS,isomer #1 | CCC(O[Si](C)(C)C(C)(C)C)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CCC(=O)C(C)(CO[Si](C)(C)C(C)(C)C)C2CC4)O1 | 4152.2 | Semi standard non polar | 33892256 | (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione,2TBDMS,isomer #2 | CCC(O[Si](C)(C)C(C)(C)C)C1CC(C)C2(C=C(O[Si](C)(C)C(C)(C)C)C3(C)C4=C(CCC32C)C2(C)CCC(=O)C(C)(CO)C2CC4)O1 | 4081.0 | Semi standard non polar | 33892256 | (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione,2TBDMS,isomer #3 | CCC(O[Si](C)(C)C(C)(C)C)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(CO)C2CC4)O1 | 4134.7 | Semi standard non polar | 33892256 | (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione,2TBDMS,isomer #4 | CCC(O)C1CC(C)C2(C=C(O[Si](C)(C)C(C)(C)C)C3(C)C4=C(CCC32C)C2(C)CCC(=O)C(C)(CO[Si](C)(C)C(C)(C)C)C2CC4)O1 | 4009.9 | Semi standard non polar | 33892256 | (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione,2TBDMS,isomer #5 | CCC(O)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(CO[Si](C)(C)C(C)(C)C)C2CC4)O1 | 4074.5 | Semi standard non polar | 33892256 | (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione,2TBDMS,isomer #6 | CCC(O)C1CC(C)C2(C=C(O[Si](C)(C)C(C)(C)C)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(CO)C2CC4)O1 | 3978.8 | Semi standard non polar | 33892256 | (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione,3TBDMS,isomer #1 | CCC(O[Si](C)(C)C(C)(C)C)C1CC(C)C2(C=C(O[Si](C)(C)C(C)(C)C)C3(C)C4=C(CCC32C)C2(C)CCC(=O)C(C)(CO[Si](C)(C)C(C)(C)C)C2CC4)O1 | 4213.4 | Semi standard non polar | 33892256 | (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione,3TBDMS,isomer #1 | CCC(O[Si](C)(C)C(C)(C)C)C1CC(C)C2(C=C(O[Si](C)(C)C(C)(C)C)C3(C)C4=C(CCC32C)C2(C)CCC(=O)C(C)(CO[Si](C)(C)C(C)(C)C)C2CC4)O1 | 4172.7 | Standard non polar | 33892256 | (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione,3TBDMS,isomer #2 | CCC(O[Si](C)(C)C(C)(C)C)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(CO[Si](C)(C)C(C)(C)C)C2CC4)O1 | 4274.1 | Semi standard non polar | 33892256 | (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione,3TBDMS,isomer #2 | CCC(O[Si](C)(C)C(C)(C)C)C1CC(C)C2(CC(=O)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(CO[Si](C)(C)C(C)(C)C)C2CC4)O1 | 4070.3 | Standard non polar | 33892256 | (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione,3TBDMS,isomer #3 | CCC(O[Si](C)(C)C(C)(C)C)C1CC(C)C2(C=C(O[Si](C)(C)C(C)(C)C)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(CO)C2CC4)O1 | 4171.3 | Semi standard non polar | 33892256 | (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione,3TBDMS,isomer #3 | CCC(O[Si](C)(C)C(C)(C)C)C1CC(C)C2(C=C(O[Si](C)(C)C(C)(C)C)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(CO)C2CC4)O1 | 3904.8 | Standard non polar | 33892256 | (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione,3TBDMS,isomer #4 | CCC(O)C1CC(C)C2(C=C(O[Si](C)(C)C(C)(C)C)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(CO[Si](C)(C)C(C)(C)C)C2CC4)O1 | 4127.7 | Semi standard non polar | 33892256 | (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione,3TBDMS,isomer #4 | CCC(O)C1CC(C)C2(C=C(O[Si](C)(C)C(C)(C)C)C3(C)C4=C(CCC32C)C2(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(CO[Si](C)(C)C(C)(C)C)C2CC4)O1 | 3916.2 | Standard non polar | 33892256 |
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| GC-MS SpectraSpectrum Type | Description | Splash Key | Deposition Date | Source | View |
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Predicted GC-MS | Predicted GC-MS Spectrum - (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione GC-MS (Non-derivatized) - 70eV, Positive | splash10-007x-2116900000-54d51b08d128b8a2f992 | 2017-09-01 | Wishart Lab | View Spectrum | Predicted GC-MS | Predicted GC-MS Spectrum - (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione GC-MS (2 TMS) - 70eV, Positive | splash10-0uk9-3345597000-59fda9502debd952d858 | 2017-10-06 | Wishart Lab | View Spectrum | Predicted GC-MS | Predicted GC-MS Spectrum - (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione GC-MS (Non-derivatized) - 70eV, Positive | Not Available | 2021-10-12 | Wishart Lab | View Spectrum | Predicted GC-MS | Predicted GC-MS Spectrum - (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione GC-MS (Non-derivatized) - 70eV, Positive | Not Available | 2021-10-12 | Wishart Lab | View Spectrum |
MS/MS SpectraSpectrum Type | Description | Splash Key | Deposition Date | Source | View |
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Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione 10V, Positive-QTOF | splash10-0ab9-0001900000-5b683f06a4d4836c3236 | 2016-08-02 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione 20V, Positive-QTOF | splash10-0a5l-3029800000-7091e54d37c163d3ef76 | 2016-08-02 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione 40V, Positive-QTOF | splash10-05tv-5097100000-a0af3823c1a2fcfa1b35 | 2016-08-02 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione 10V, Negative-QTOF | splash10-00di-0000900000-d8aa911bffd98338dad2 | 2016-08-03 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione 20V, Negative-QTOF | splash10-0fkc-1001900000-7d810894cfbcab002589 | 2016-08-03 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione 40V, Negative-QTOF | splash10-0a4u-4019300000-a7402b971fd09a499b16 | 2016-08-03 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione 10V, Negative-QTOF | splash10-00di-0000900000-91947a5f3574d4c5169f | 2021-09-23 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione 20V, Negative-QTOF | splash10-03e9-1003900000-5060fb0a7606e09a8272 | 2021-09-23 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione 40V, Negative-QTOF | splash10-0a4i-8001900000-bd64ed6193996190ce40 | 2021-09-23 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione 10V, Positive-QTOF | splash10-05fr-0001900000-5216cf534de15e031eb0 | 2021-09-24 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione 20V, Positive-QTOF | splash10-0a4i-0033900000-94088580e13427050651 | 2021-09-24 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - (23S,24S)-17,23-Epoxy-24,29-dihydroxy-27-norlanost-8-ene-3,15-dione 40V, Positive-QTOF | splash10-000f-9243800000-3d8a264bdda8c0d8fee5 | 2021-09-24 | Wishart Lab | View Spectrum |
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