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 20:48:16 UTC |
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Update Date | 2022-03-07 02:54:37 UTC |
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HMDB ID | HMDB0035782 |
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Secondary Accession Numbers | |
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Metabolite Identification |
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Common Name | Esculentic acid (Diplazium) |
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Description | 10,11-dihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-icosahydropicene-4a-carboxylic acid belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. Based on a literature review very few articles have been published on 10,11-dihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-icosahydropicene-4a-carboxylic acid. |
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Structure | CC1CCC2(CCC3(C)C(=CCC4C5(C)CC(O)C(O)C(C)(CO)C5CCC34C)C2C1C)C(O)=O InChI=1S/C30H48O5/c1-17-9-12-30(25(34)35)14-13-28(5)19(23(30)18(17)2)7-8-22-26(3)15-20(32)24(33)27(4,16-31)21(26)10-11-29(22,28)6/h7,17-18,20-24,31-33H,8-16H2,1-6H3,(H,34,35) |
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Synonyms | Value | Source |
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10,11-Dihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-icosahydropicene-4a-carboxylate | Generator | Esculentate (diplazium) | Generator |
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Chemical Formula | C30H48O5 |
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Average Molecular Weight | 488.6991 |
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Monoisotopic Molecular Weight | 488.350174646 |
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IUPAC Name | 10,11-dihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-icosahydropicene-4a-carboxylic acid |
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Traditional Name | asiatic acid |
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CAS Registry Number | 76964-07-3 |
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SMILES | CC1CCC2(CCC3(C)C(=CCC4C5(C)CC(O)C(O)C(C)(CO)C5CCC34C)C2C1C)C(O)=O |
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InChI Identifier | InChI=1S/C30H48O5/c1-17-9-12-30(25(34)35)14-13-28(5)19(23(30)18(17)2)7-8-22-26(3)15-20(32)24(33)27(4,16-31)21(26)10-11-29(22,28)6/h7,17-18,20-24,31-33H,8-16H2,1-6H3,(H,34,35) |
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InChI Key | JXSVIVRDWWRQRT-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 | |
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Substituents | - Triterpenoid
- 12-hydroxysteroid
- Hydroxysteroid
- Steroid
- Cyclic alcohol
- Secondary alcohol
- Carboxylic acid derivative
- Carboxylic acid
- Monocarboxylic acid or derivatives
- Hydrocarbon derivative
- Organic oxide
- Organic oxygen compound
- Alcohol
- Carbonyl group
- Organooxygen compound
- Primary 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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Ontology |
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Physiological effect | Not Available |
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Disposition | |
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Process | Not Available |
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Role | Not Available |
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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 | 270 °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 | | Show more...
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Predicted Chromatographic Properties | Predicted Collision Cross SectionsPredicted Kovats Retention IndicesUnderivatizedDerivatizedDerivative Name / Structure | SMILES | Kovats RI Value | Column Type | Reference |
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Esculentic acid (Diplazium),1TMS,isomer #1 | CC1CCC2(C(=O)O)CCC3(C)C(=CCC4C5(C)CC(O[Si](C)(C)C)C(O)C(C)(CO)C5CCC43C)C2C1C | 4188.4 | Semi standard non polar | 33892256 | Esculentic acid (Diplazium),1TMS,isomer #2 | CC1CCC2(C(=O)O)CCC3(C)C(=CCC4C5(C)CC(O)C(O[Si](C)(C)C)C(C)(CO)C5CCC43C)C2C1C | 4190.9 | Semi standard non polar | 33892256 | Esculentic acid (Diplazium),1TMS,isomer #3 | CC1CCC2(C(=O)O)CCC3(C)C(=CCC4C5(C)CC(O)C(O)C(C)(CO[Si](C)(C)C)C5CCC43C)C2C1C | 4181.8 | Semi standard non polar | 33892256 | Esculentic acid (Diplazium),1TMS,isomer #4 | CC1CCC2(C(=O)O[Si](C)(C)C)CCC3(C)C(=CCC4C5(C)CC(O)C(O)C(C)(CO)C5CCC43C)C2C1C | 4092.7 | Semi standard non polar | 33892256 | Esculentic acid (Diplazium),2TMS,isomer #1 | CC1CCC2(C(=O)O[Si](C)(C)C)CCC3(C)C(=CCC4C5(C)CC(O[Si](C)(C)C)C(O)C(C)(CO)C5CCC43C)C2C1C | 4072.3 | Semi standard non polar | 33892256 | Esculentic acid (Diplazium),2TMS,isomer #2 | CC1CCC2(C(=O)O)CCC3(C)C(=CCC4C5(C)CC(O[Si](C)(C)C)C(O[Si](C)(C)C)C(C)(CO)C5CCC43C)C2C1C | 4201.6 | Semi standard non polar | 33892256 | Esculentic acid (Diplazium),2TMS,isomer #3 | CC1CCC2(C(=O)O)CCC3(C)C(=CCC4C5(C)CC(O[Si](C)(C)C)C(O)C(C)(CO[Si](C)(C)C)C5CCC43C)C2C1C | 4207.9 | Semi standard non polar | 33892256 | Esculentic acid (Diplazium),2TMS,isomer #4 | CC1CCC2(C(=O)O[Si](C)(C)C)CCC3(C)C(=CCC4C5(C)CC(O)C(O[Si](C)(C)C)C(C)(CO)C5CCC43C)C2C1C | 4074.8 | Semi standard non polar | 33892256 | Esculentic acid (Diplazium),2TMS,isomer #5 | CC1CCC2(C(=O)O)CCC3(C)C(=CCC4C5(C)CC(O)C(O[Si](C)(C)C)C(C)(CO[Si](C)(C)C)C5CCC43C)C2C1C | 4203.0 | Semi standard non polar | 33892256 | Esculentic acid (Diplazium),2TMS,isomer #6 | CC1CCC2(C(=O)O[Si](C)(C)C)CCC3(C)C(=CCC4C5(C)CC(O)C(O)C(C)(CO[Si](C)(C)C)C5CCC43C)C2C1C | 4122.2 | Semi standard non polar | 33892256 | Esculentic acid (Diplazium),3TMS,isomer #1 | CC1CCC2(C(=O)O[Si](C)(C)C)CCC3(C)C(=CCC4C5(C)CC(O[Si](C)(C)C)C(O[Si](C)(C)C)C(C)(CO)C5CCC43C)C2C1C | 4017.6 | Semi standard non polar | 33892256 | Esculentic acid (Diplazium),3TMS,isomer #2 | CC1CCC2(C(=O)O[Si](C)(C)C)CCC3(C)C(=CCC4C5(C)CC(O[Si](C)(C)C)C(O)C(C)(CO[Si](C)(C)C)C5CCC43C)C2C1C | 4021.5 | Semi standard non polar | 33892256 | Esculentic acid (Diplazium),3TMS,isomer #3 | CC1CCC2(C(=O)O)CCC3(C)C(=CCC4C5(C)CC(O[Si](C)(C)C)C(O[Si](C)(C)C)C(C)(CO[Si](C)(C)C)C5CCC43C)C2C1C | 4182.9 | Semi standard non polar | 33892256 | Esculentic acid (Diplazium),3TMS,isomer #4 | CC1CCC2(C(=O)O[Si](C)(C)C)CCC3(C)C(=CCC4C5(C)CC(O)C(O[Si](C)(C)C)C(C)(CO[Si](C)(C)C)C5CCC43C)C2C1C | 4016.8 | Semi standard non polar | 33892256 | Esculentic acid (Diplazium),4TMS,isomer #1 | CC1CCC2(C(=O)O[Si](C)(C)C)CCC3(C)C(=CCC4C5(C)CC(O[Si](C)(C)C)C(O[Si](C)(C)C)C(C)(CO[Si](C)(C)C)C5CCC43C)C2C1C | 3980.1 | Semi standard non polar | 33892256 | Esculentic acid (Diplazium),1TBDMS,isomer #1 | CC1CCC2(C(=O)O)CCC3(C)C(=CCC4C5(C)CC(O[Si](C)(C)C(C)(C)C)C(O)C(C)(CO)C5CCC43C)C2C1C | 4405.0 | Semi standard non polar | 33892256 | Esculentic acid (Diplazium),1TBDMS,isomer #2 | CC1CCC2(C(=O)O)CCC3(C)C(=CCC4C5(C)CC(O)C(O[Si](C)(C)C(C)(C)C)C(C)(CO)C5CCC43C)C2C1C | 4409.5 | Semi standard non polar | 33892256 | Esculentic acid (Diplazium),1TBDMS,isomer #3 | CC1CCC2(C(=O)O)CCC3(C)C(=CCC4C5(C)CC(O)C(O)C(C)(CO[Si](C)(C)C(C)(C)C)C5CCC43C)C2C1C | 4421.5 | Semi standard non polar | 33892256 | Esculentic acid (Diplazium),1TBDMS,isomer #4 | CC1CCC2(C(=O)O[Si](C)(C)C(C)(C)C)CCC3(C)C(=CCC4C5(C)CC(O)C(O)C(C)(CO)C5CCC43C)C2C1C | 4342.0 | Semi standard non polar | 33892256 | Esculentic acid (Diplazium),2TBDMS,isomer #1 | CC1CCC2(C(=O)O[Si](C)(C)C(C)(C)C)CCC3(C)C(=CCC4C5(C)CC(O[Si](C)(C)C(C)(C)C)C(O)C(C)(CO)C5CCC43C)C2C1C | 4523.4 | Semi standard non polar | 33892256 | Esculentic acid (Diplazium),2TBDMS,isomer #2 | CC1CCC2(C(=O)O)CCC3(C)C(=CCC4C5(C)CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(C)(CO)C5CCC43C)C2C1C | 4633.6 | Semi standard non polar | 33892256 | Esculentic acid (Diplazium),2TBDMS,isomer #3 | CC1CCC2(C(=O)O)CCC3(C)C(=CCC4C5(C)CC(O[Si](C)(C)C(C)(C)C)C(O)C(C)(CO[Si](C)(C)C(C)(C)C)C5CCC43C)C2C1C | 4643.1 | Semi standard non polar | 33892256 | Esculentic acid (Diplazium),2TBDMS,isomer #4 | CC1CCC2(C(=O)O[Si](C)(C)C(C)(C)C)CCC3(C)C(=CCC4C5(C)CC(O)C(O[Si](C)(C)C(C)(C)C)C(C)(CO)C5CCC43C)C2C1C | 4531.8 | Semi standard non polar | 33892256 | Esculentic acid (Diplazium),2TBDMS,isomer #5 | CC1CCC2(C(=O)O)CCC3(C)C(=CCC4C5(C)CC(O)C(O[Si](C)(C)C(C)(C)C)C(C)(CO[Si](C)(C)C(C)(C)C)C5CCC43C)C2C1C | 4640.7 | Semi standard non polar | 33892256 | Esculentic acid (Diplazium),2TBDMS,isomer #6 | CC1CCC2(C(=O)O[Si](C)(C)C(C)(C)C)CCC3(C)C(=CCC4C5(C)CC(O)C(O)C(C)(CO[Si](C)(C)C(C)(C)C)C5CCC43C)C2C1C | 4582.8 | Semi standard non polar | 33892256 | Esculentic acid (Diplazium),3TBDMS,isomer #1 | CC1CCC2(C(=O)O[Si](C)(C)C(C)(C)C)CCC3(C)C(=CCC4C5(C)CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(C)(CO)C5CCC43C)C2C1C | 4654.5 | Semi standard non polar | 33892256 | Esculentic acid (Diplazium),3TBDMS,isomer #2 | CC1CCC2(C(=O)O[Si](C)(C)C(C)(C)C)CCC3(C)C(=CCC4C5(C)CC(O[Si](C)(C)C(C)(C)C)C(O)C(C)(CO[Si](C)(C)C(C)(C)C)C5CCC43C)C2C1C | 4652.6 | Semi standard non polar | 33892256 | Esculentic acid (Diplazium),3TBDMS,isomer #3 | CC1CCC2(C(=O)O)CCC3(C)C(=CCC4C5(C)CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(C)(CO[Si](C)(C)C(C)(C)C)C5CCC43C)C2C1C | 4813.7 | Semi standard non polar | 33892256 | Esculentic acid (Diplazium),3TBDMS,isomer #4 | CC1CCC2(C(=O)O[Si](C)(C)C(C)(C)C)CCC3(C)C(=CCC4C5(C)CC(O)C(O[Si](C)(C)C(C)(C)C)C(C)(CO[Si](C)(C)C(C)(C)C)C5CCC43C)C2C1C | 4668.1 | Semi standard non polar | 33892256 |
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Spectra |
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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 - Esculentic acid (Diplazium) GC-MS (Non-derivatized) - 70eV, Positive | splash10-05fr-1002900000-3509f4eb5cbfeb47ea78 | 2017-09-01 | Wishart Lab | View Spectrum | Predicted GC-MS | Predicted GC-MS Spectrum - Esculentic acid (Diplazium) GC-MS (2 TMS) - 70eV, Positive | splash10-014i-2000139000-c1d450a2a7a6dc4b0457 | 2017-10-06 | Wishart Lab | View Spectrum | Predicted GC-MS | Predicted GC-MS Spectrum - Esculentic acid (Diplazium) GC-MS (Non-derivatized) - 70eV, Positive | Not Available | 2021-10-12 | Wishart Lab | View Spectrum | Predicted GC-MS | Predicted GC-MS Spectrum - Esculentic acid (Diplazium) GC-MS (Non-derivatized) - 70eV, Positive | Not Available | 2021-10-12 | Wishart Lab | View Spectrum | Predicted GC-MS | Predicted GC-MS Spectrum - Esculentic acid (Diplazium) 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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Experimental LC-MS/MS | LC-MS/MS Spectrum - Esculentic acid (Diplazium) LC-ESI-QTOF , negative-QTOF | splash10-000i-0000900000-3283f3a6fdc1f8a664da | 2017-09-14 | HMDB team, MONA | View Spectrum | Experimental LC-MS/MS | LC-MS/MS Spectrum - Esculentic acid (Diplazium) LC-ESI-QTOF , negative-QTOF | splash10-000i-0000900000-baec48f0cfa32ffc5615 | 2017-09-14 | HMDB team, MONA | View Spectrum | Experimental LC-MS/MS | LC-MS/MS Spectrum - Esculentic acid (Diplazium) LC-ESI-QTOF , negative-QTOF | splash10-000i-0000900000-76fefa4e9e70b86438fc | 2017-09-14 | HMDB team, MONA | View Spectrum | Experimental LC-MS/MS | LC-MS/MS Spectrum - Esculentic acid (Diplazium) Linear Ion Trap , negative-QTOF | splash10-0a4i-0003900000-bc4bc63229c155c0d500 | 2017-09-14 | HMDB team, MONA | View Spectrum | Experimental LC-MS/MS | LC-MS/MS Spectrum - Esculentic acid (Diplazium) LC-ESI-TOF , negative-QTOF | splash10-000i-0000910000-df7ce2b45192539f1338 | 2017-09-14 | HMDB team, MONA | View Spectrum | Experimental LC-MS/MS | LC-MS/MS Spectrum - Esculentic acid (Diplazium) LC-ESI-TOF , negative-QTOF | splash10-000i-0000900000-b0d9347334d99f0e9638 | 2017-09-14 | HMDB team, MONA | View Spectrum | Experimental LC-MS/MS | LC-MS/MS Spectrum - Esculentic acid (Diplazium) LC-ESI-QTOF , positive-QTOF | splash10-03di-0000090000-d986660f9cea818e4187 | 2017-09-14 | HMDB team, MONA | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Esculentic acid (Diplazium) 10V, Positive-QTOF | splash10-0fki-0000900000-4650ac5b3e7da78820be | 2015-04-24 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Esculentic acid (Diplazium) 20V, Positive-QTOF | splash10-0umi-0000900000-f42a60f764ea4933fdd9 | 2015-04-24 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Esculentic acid (Diplazium) 40V, Positive-QTOF | splash10-05di-2312900000-2f4b2077f86f4e9e29ed | 2015-04-24 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Esculentic acid (Diplazium) 10V, Positive-QTOF | splash10-0fki-0000900000-4650ac5b3e7da78820be | 2015-04-24 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Esculentic acid (Diplazium) 20V, Positive-QTOF | splash10-0umi-0000900000-f42a60f764ea4933fdd9 | 2015-04-24 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Esculentic acid (Diplazium) 40V, Positive-QTOF | splash10-05di-2312900000-2f4b2077f86f4e9e29ed | 2015-04-24 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Esculentic acid (Diplazium) 10V, Positive-QTOF | splash10-0fki-0000900000-4650ac5b3e7da78820be | 2015-04-24 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Esculentic acid (Diplazium) 20V, Positive-QTOF | splash10-0umi-0000900000-f42a60f764ea4933fdd9 | 2015-04-24 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Esculentic acid (Diplazium) 40V, Positive-QTOF | splash10-05di-2312900000-2f4b2077f86f4e9e29ed | 2015-04-24 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Esculentic acid (Diplazium) 10V, Negative-QTOF | splash10-000i-0000900000-da8204c2688cd58099c0 | 2015-04-25 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Esculentic acid (Diplazium) 20V, Negative-QTOF | splash10-02bu-0000900000-2ec7163c25cff3f73cb0 | 2015-04-25 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Esculentic acid (Diplazium) 40V, Negative-QTOF | splash10-03di-1000900000-d701ce94f1b5864470e5 | 2015-04-25 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Esculentic acid (Diplazium) 10V, Negative-QTOF | splash10-000i-0000900000-da8204c2688cd58099c0 | 2015-04-25 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Esculentic acid (Diplazium) 20V, Negative-QTOF | splash10-02bu-0000900000-2ec7163c25cff3f73cb0 | 2015-04-25 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Esculentic acid (Diplazium) 40V, Negative-QTOF | splash10-03di-1000900000-d701ce94f1b5864470e5 | 2015-04-25 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Esculentic acid (Diplazium) 10V, Negative-QTOF | splash10-000i-0000900000-da8204c2688cd58099c0 | 2015-04-25 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Esculentic acid (Diplazium) 20V, Negative-QTOF | splash10-02bu-0000900000-2ec7163c25cff3f73cb0 | 2015-04-25 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Esculentic acid (Diplazium) 40V, Negative-QTOF | splash10-03di-1000900000-d701ce94f1b5864470e5 | 2015-04-25 | Wishart Lab | View Spectrum |
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Biological Properties |
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Cellular Locations | |
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Biospecimen Locations | Not Available |
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Tissue Locations | Not Available |
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Pathways | |
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Normal Concentrations |
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Abnormal Concentrations |
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Associated Disorders and Diseases |
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Disease References | None |
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Associated OMIM IDs | None |
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External Links |
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DrugBank ID | Not Available |
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Phenol Explorer Compound ID | Not Available |
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FooDB ID | Not Available |
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KNApSAcK ID | Not Available |
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Chemspider ID | 261424 |
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KEGG Compound ID | Not Available |
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BioCyc ID | Not Available |
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BiGG ID | Not Available |
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Wikipedia Link | Not Available |
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METLIN ID | Not Available |
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PubChem Compound | 296191 |
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PDB ID | Not Available |
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ChEBI ID | Not Available |
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Food Biomarker Ontology | Not Available |
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VMH ID | Not Available |
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MarkerDB ID | Not Available |
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Good Scents ID | Not Available |
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References |
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Synthesis Reference | Not Available |
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Material Safety Data Sheet (MSDS) | Not Available |
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General References | - Simons K, Toomre D: Lipid rafts and signal transduction. Nat Rev Mol Cell Biol. 2000 Oct;1(1):31-9. [PubMed:11413487 ]
- Watson AD: Thematic review series: systems biology approaches to metabolic and cardiovascular disorders. Lipidomics: a global approach to lipid analysis in biological systems. J Lipid Res. 2006 Oct;47(10):2101-11. Epub 2006 Aug 10. [PubMed:16902246 ]
- Sethi JK, Vidal-Puig AJ: Thematic review series: adipocyte biology. Adipose tissue function and plasticity orchestrate nutritional adaptation. J Lipid Res. 2007 Jun;48(6):1253-62. Epub 2007 Mar 20. [PubMed:17374880 ]
- Lingwood D, Simons K: Lipid rafts as a membrane-organizing principle. Science. 2010 Jan 1;327(5961):46-50. doi: 10.1126/science.1174621. [PubMed:20044567 ]
- (). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .
- Gunstone, Frank D., John L. Harwood, and Albert J. Dijkstra (2007). The lipid handbook with CD-ROM. CRC Press.
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