Record Information |
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Version | 5.0 |
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Status | Expected but not Quantified |
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Creation Date | 2012-09-12 01:02:09 UTC |
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Update Date | 2022-03-07 02:56:15 UTC |
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HMDB ID | HMDB0039546 |
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Secondary Accession Numbers | |
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Metabolite Identification |
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Common Name | Ginsenoside Rg3 |
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Description | Ginsenoside Rg3 belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. Based on a literature review a significant number of articles have been published on Ginsenoside Rg3. |
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Structure | CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O)C4OC4OC(CO)C(O)C(O)C4O)C(C)(C)C3CCC21C InChI=1S/C42H72O13/c1-21(2)10-9-14-42(8,51)22-11-16-41(7)29(22)23(45)18-27-39(5)15-13-28(38(3,4)26(39)12-17-40(27,41)6)54-37-35(33(49)31(47)25(20-44)53-37)55-36-34(50)32(48)30(46)24(19-43)52-36/h10,22-37,43-51H,9,11-20H2,1-8H3 |
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Synonyms | Value | Source |
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(20S)-Propanaxadiol | HMDB | Ginsenoside RG(3) | MeSH, HMDB | 20(S)-Ginsenoside RG(3) | MeSH, HMDB | 3-O-beta-D-Glucopyranosyl-(1->2)-beta-D-glucopyranosyldammar-24-ene-3beta,12beta,20S-triol | MeSH | Ginsenoside 20-RG3 | MeSH | 20S-Ginsenoside RG3 | MeSH | S-Ginsenoside RG3 | MeSH | 20(R)-Ginsenoside RG(3) | MeSH | Ginsenoside RG3 | MeSH |
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Chemical Formula | C42H72O13 |
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Average Molecular Weight | 785.0133 |
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Monoisotopic Molecular Weight | 784.49729239 |
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IUPAC Name | 2-[(4,5-dihydroxy-2-{[16-hydroxy-14-(2-hydroxy-6-methylhept-5-en-2-yl)-2,6,6,10,11-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-5-yl]oxy}-6-(hydroxymethyl)oxan-3-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol |
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Traditional Name | 2-[(4,5-dihydroxy-2-{[16-hydroxy-14-(2-hydroxy-6-methylhept-5-en-2-yl)-2,6,6,10,11-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-5-yl]oxy}-6-(hydroxymethyl)oxan-3-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol |
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CAS Registry Number | 14197-60-5 |
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SMILES | CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O)C4OC4OC(CO)C(O)C(O)C4O)C(C)(C)C3CCC21C |
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InChI Identifier | InChI=1S/C42H72O13/c1-21(2)10-9-14-42(8,51)22-11-16-41(7)29(22)23(45)18-27-39(5)15-13-28(38(3,4)26(39)12-17-40(27,41)6)54-37-35(33(49)31(47)25(20-44)53-37)55-36-34(50)32(48)30(46)24(19-43)52-36/h10,22-37,43-51H,9,11-20H2,1-8H3 |
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InChI Key | RWXIFXNRCLMQCD-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
- Steroidal glycoside
- 20-hydroxysteroid
- 12-hydroxysteroid
- Hydroxysteroid
- Steroid
- Disaccharide
- Glycosyl compound
- O-glycosyl compound
- Oxane
- Cyclic alcohol
- Tertiary alcohol
- Secondary alcohol
- Polyol
- Oxacycle
- Acetal
- Organoheterocyclic compound
- Primary alcohol
- Organooxygen compound
- Hydrocarbon derivative
- Organic oxygen compound
- Alcohol
- Aliphatic heteropolycyclic compound
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Molecular Framework | Aliphatic heteropolycyclic compounds |
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External Descriptors | |
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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 | 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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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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Ginsenoside Rg3,1TMS,isomer #1 | CC(C)=CCCC(C)(O[Si](C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O)C4OC4OC(CO)C(O)C(O)C4O)C(C)(C)C3CCC12C | 5923.4 | Semi standard non polar | 33892256 | Ginsenoside Rg3,1TMS,isomer #1 | CC(C)=CCCC(C)(O[Si](C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O)C4OC4OC(CO)C(O)C(O)C4O)C(C)(C)C3CCC12C | 5516.7 | Standard non polar | 33892256 | Ginsenoside Rg3,1TMS,isomer #2 | CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C)CC1C3(C)CCC(OC4OC(CO)C(O)C(O)C4OC4OC(CO)C(O)C(O)C4O)C(C)(C)C3CCC12C | 5902.0 | Semi standard non polar | 33892256 | Ginsenoside Rg3,1TMS,isomer #2 | CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C)CC1C3(C)CCC(OC4OC(CO)C(O)C(O)C4OC4OC(CO)C(O)C(O)C4O)C(C)(C)C3CCC12C | 5435.9 | Standard non polar | 33892256 | Ginsenoside Rg3,1TMS,isomer #3 | CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO[Si](C)(C)C)C(O)C(O)C4OC4OC(CO)C(O)C(O)C4O)C(C)(C)C3CCC12C | 5966.7 | Semi standard non polar | 33892256 | Ginsenoside Rg3,1TMS,isomer #3 | CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO[Si](C)(C)C)C(O)C(O)C4OC4OC(CO)C(O)C(O)C4O)C(C)(C)C3CCC12C | 5536.2 | Standard non polar | 33892256 | Ginsenoside Rg3,1TMS,isomer #4 | CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4OC4OC(CO)C(O)C(O)C4O)C(C)(C)C3CCC12C | 5964.1 | Semi standard non polar | 33892256 | Ginsenoside Rg3,1TMS,isomer #4 | CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4OC4OC(CO)C(O)C(O)C4O)C(C)(C)C3CCC12C | 5498.6 | Standard non polar | 33892256 | Ginsenoside Rg3,1TMS,isomer #5 | CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4OC4OC(CO)C(O)C(O)C4O)C(C)(C)C3CCC12C | 5972.5 | Semi standard non polar | 33892256 | Ginsenoside Rg3,1TMS,isomer #5 | CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4OC4OC(CO)C(O)C(O)C4O)C(C)(C)C3CCC12C | 5474.7 | Standard non polar | 33892256 | Ginsenoside Rg3,1TMS,isomer #6 | CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O)C4OC4OC(CO[Si](C)(C)C)C(O)C(O)C4O)C(C)(C)C3CCC12C | 5959.1 | Semi standard non polar | 33892256 | Ginsenoside Rg3,1TMS,isomer #6 | CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O)C4OC4OC(CO[Si](C)(C)C)C(O)C(O)C4O)C(C)(C)C3CCC12C | 5547.3 | Standard non polar | 33892256 | Ginsenoside Rg3,1TMS,isomer #7 | CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O)C4OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C(C)(C)C3CCC12C | 5970.1 | Semi standard non polar | 33892256 | Ginsenoside Rg3,1TMS,isomer #7 | CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O)C4OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C(C)(C)C3CCC12C | 5485.3 | Standard non polar | 33892256 | Ginsenoside Rg3,1TMS,isomer #8 | CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O)C4OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C(C)(C)C3CCC12C | 5960.7 | Semi standard non polar | 33892256 | Ginsenoside Rg3,1TMS,isomer #8 | CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O)C4OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C(C)(C)C3CCC12C | 5469.8 | Standard non polar | 33892256 | Ginsenoside Rg3,1TMS,isomer #9 | CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O)C4OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C(C)(C)C3CCC12C | 5947.1 | Semi standard non polar | 33892256 | Ginsenoside Rg3,1TMS,isomer #9 | CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O)C4OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C(C)(C)C3CCC12C | 5494.6 | Standard non polar | 33892256 | Ginsenoside Rg3,1TBDMS,isomer #1 | CC(C)=CCCC(C)(O[Si](C)(C)C(C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O)C4OC4OC(CO)C(O)C(O)C4O)C(C)(C)C3CCC12C | 6130.5 | Semi standard non polar | 33892256 | Ginsenoside Rg3,1TBDMS,isomer #1 | CC(C)=CCCC(C)(O[Si](C)(C)C(C)(C)C)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O)C4OC4OC(CO)C(O)C(O)C4O)C(C)(C)C3CCC12C | 5749.4 | Standard non polar | 33892256 | Ginsenoside Rg3,1TBDMS,isomer #2 | CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C(C)(C)C)CC1C3(C)CCC(OC4OC(CO)C(O)C(O)C4OC4OC(CO)C(O)C(O)C4O)C(C)(C)C3CCC12C | 6120.7 | Semi standard non polar | 33892256 | Ginsenoside Rg3,1TBDMS,isomer #2 | CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O[Si](C)(C)C(C)(C)C)CC1C3(C)CCC(OC4OC(CO)C(O)C(O)C4OC4OC(CO)C(O)C(O)C4O)C(C)(C)C3CCC12C | 5664.1 | Standard non polar | 33892256 | Ginsenoside Rg3,1TBDMS,isomer #3 | CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C4OC4OC(CO)C(O)C(O)C4O)C(C)(C)C3CCC12C | 6135.5 | Semi standard non polar | 33892256 | Ginsenoside Rg3,1TBDMS,isomer #3 | CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C4OC4OC(CO)C(O)C(O)C4O)C(C)(C)C3CCC12C | 5761.9 | Standard non polar | 33892256 | Ginsenoside Rg3,1TBDMS,isomer #4 | CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C4OC4OC(CO)C(O)C(O)C4O)C(C)(C)C3CCC12C | 6193.3 | Semi standard non polar | 33892256 | Ginsenoside Rg3,1TBDMS,isomer #4 | CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C4OC4OC(CO)C(O)C(O)C4O)C(C)(C)C3CCC12C | 5718.0 | Standard non polar | 33892256 | Ginsenoside Rg3,1TBDMS,isomer #5 | CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C4OC4OC(CO)C(O)C(O)C4O)C(C)(C)C3CCC12C | 6198.3 | Semi standard non polar | 33892256 | Ginsenoside Rg3,1TBDMS,isomer #5 | CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C4OC4OC(CO)C(O)C(O)C4O)C(C)(C)C3CCC12C | 5694.2 | Standard non polar | 33892256 | Ginsenoside Rg3,1TBDMS,isomer #6 | CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O)C4OC4OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C4O)C(C)(C)C3CCC12C | 6125.2 | Semi standard non polar | 33892256 | Ginsenoside Rg3,1TBDMS,isomer #6 | CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O)C4OC4OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C4O)C(C)(C)C3CCC12C | 5776.5 | Standard non polar | 33892256 | Ginsenoside Rg3,1TBDMS,isomer #7 | CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O)C4OC4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C4O)C(C)(C)C3CCC12C | 6201.2 | Semi standard non polar | 33892256 | Ginsenoside Rg3,1TBDMS,isomer #7 | CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O)C4OC4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C4O)C(C)(C)C3CCC12C | 5709.2 | Standard non polar | 33892256 | Ginsenoside Rg3,1TBDMS,isomer #8 | CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O)C4OC4OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C4O)C(C)(C)C3CCC12C | 6187.9 | Semi standard non polar | 33892256 | Ginsenoside Rg3,1TBDMS,isomer #8 | CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O)C4OC4OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C4O)C(C)(C)C3CCC12C | 5689.2 | Standard non polar | 33892256 | Ginsenoside Rg3,1TBDMS,isomer #9 | CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O)C4OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C(C)(C)C)C(C)(C)C3CCC12C | 6174.0 | Semi standard non polar | 33892256 | Ginsenoside Rg3,1TBDMS,isomer #9 | CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC1C3(C)CCC(OC4OC(CO)C(O)C(O)C4OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C(C)(C)C)C(C)(C)C3CCC12C | 5714.6 | Standard non polar | 33892256 |
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Spectra |
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| MS/MS SpectraSpectrum Type | Description | Splash Key | Deposition Date | Source | View |
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Experimental LC-MS/MS | LC-MS/MS Spectrum - Ginsenoside Rg3 6V, Positive-QTOF | splash10-001i-0000000900-6cad35fcf6f2a4e5f1fa | 2021-09-20 | HMDB team, MONA | View Spectrum | Experimental LC-MS/MS | LC-MS/MS Spectrum - Ginsenoside Rg3 6V, Positive-QTOF | splash10-001i-1700001900-fb630b7936bac95faf72 | 2021-09-20 | HMDB team, MONA | View Spectrum | Experimental LC-MS/MS | LC-MS/MS Spectrum - Ginsenoside Rg3 6V, Positive-QTOF | splash10-001i-0100000900-5add41801d1b174622f9 | 2021-09-20 | HMDB team, MONA | View Spectrum | Experimental LC-MS/MS | LC-MS/MS Spectrum - Ginsenoside Rg3 6V, Positive-QTOF | splash10-001i-0300001900-38b430171668c48db644 | 2021-09-20 | HMDB team, MONA | View Spectrum | Experimental LC-MS/MS | LC-MS/MS Spectrum - Ginsenoside Rg3 6V, Positive-QTOF | splash10-001i-0000000900-b6be6d2b1e555b2b15a2 | 2021-09-20 | HMDB team, MONA | View Spectrum | Experimental LC-MS/MS | LC-MS/MS Spectrum - Ginsenoside Rg3 6V, Positive-QTOF | splash10-001i-0000000900-6888ea5f3d88fec7aacd | 2021-09-20 | HMDB team, MONA | View Spectrum | Experimental LC-MS/MS | LC-MS/MS Spectrum - Ginsenoside Rg3 6V, Positive-QTOF | splash10-001i-0000000900-5f27b30935f1e5d7b795 | 2021-09-20 | HMDB team, MONA | View Spectrum | Experimental LC-MS/MS | LC-MS/MS Spectrum - Ginsenoside Rg3 6V, Positive-QTOF | splash10-001i-0000000900-2ade2cb5ef249d367f8d | 2021-09-20 | HMDB team, MONA | View Spectrum | Experimental LC-MS/MS | LC-MS/MS Spectrum - Ginsenoside Rg3 6V, Positive-QTOF | splash10-001i-0000000900-f8ed6d33fdb661d92913 | 2021-09-20 | HMDB team, MONA | View Spectrum | Experimental LC-MS/MS | LC-MS/MS Spectrum - Ginsenoside Rg3 6V, Positive-QTOF | splash10-001i-1400003900-fcff744a61411f064c86 | 2021-09-20 | HMDB team, MONA | View Spectrum | Experimental LC-MS/MS | LC-MS/MS Spectrum - Ginsenoside Rg3 6V, Positive-QTOF | splash10-0udi-3901100000-a8621455af5e27f085bb | 2021-09-20 | HMDB team, MONA | View Spectrum | Experimental LC-MS/MS | LC-MS/MS Spectrum - Ginsenoside Rg3 6V, Negative-QTOF | splash10-001i-0100000900-dc4011e9b9c0b7686d82 | 2021-09-20 | HMDB team, MONA | View Spectrum | Experimental LC-MS/MS | LC-MS/MS Spectrum - Ginsenoside Rg3 6V, Positive-QTOF | splash10-001i-0700103900-1dfac3bde0a4ead35d78 | 2021-09-20 | HMDB team, MONA | View Spectrum | Experimental LC-MS/MS | LC-MS/MS Spectrum - Ginsenoside Rg3 6V, Positive-QTOF | splash10-0ufr-3901100000-48278bcb5ea65c57e50d | 2021-09-20 | HMDB team, MONA | View Spectrum | Experimental LC-MS/MS | LC-MS/MS Spectrum - Ginsenoside Rg3 6V, Positive-QTOF | splash10-001i-1500001900-5fc4a0e40d9920b0e8d3 | 2021-09-20 | HMDB team, MONA | View Spectrum | Experimental LC-MS/MS | LC-MS/MS Spectrum - Ginsenoside Rg3 6V, Positive-QTOF | splash10-03di-1901100000-b6871ba8a802f0bd7fa9 | 2021-09-20 | HMDB team, MONA | View Spectrum | Experimental LC-MS/MS | LC-MS/MS Spectrum - Ginsenoside Rg3 6V, Positive-QTOF | splash10-0zfr-3901200000-5a3d1ed3081bd4af16e4 | 2021-09-20 | HMDB team, MONA | View Spectrum | Experimental LC-MS/MS | LC-MS/MS Spectrum - Ginsenoside Rg3 6V, Positive-QTOF | splash10-0udi-5900100000-e3f40d60ae656a012776 | 2021-09-20 | HMDB team, MONA | View Spectrum | Experimental LC-MS/MS | LC-MS/MS Spectrum - Ginsenoside Rg3 6V, Positive-QTOF | splash10-001i-0000000900-3d886264f7e0c5fbfd80 | 2021-09-20 | HMDB team, MONA | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Ginsenoside Rg3 10V, Positive-QTOF | splash10-07bo-0100915800-cfb7da67c4a0ab821bf1 | 2015-04-24 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Ginsenoside Rg3 20V, Positive-QTOF | splash10-06r6-0101904100-bee1910d421f99776736 | 2015-04-24 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Ginsenoside Rg3 40V, Positive-QTOF | splash10-03di-2301902100-f648dec5ddc13f98d2c2 | 2015-04-24 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Ginsenoside Rg3 10V, Negative-QTOF | splash10-0kx3-1500918800-cac4373dd1b84ab80413 | 2015-04-25 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Ginsenoside Rg3 20V, Negative-QTOF | splash10-0m06-1700914200-f9feb17b421146db9ba0 | 2015-04-25 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Ginsenoside Rg3 40V, Negative-QTOF | splash10-0a4l-4600900000-a6f75561d389bc04cffe | 2015-04-25 | Wishart Lab | View Spectrum |
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Biological Properties |
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Cellular Locations | - Cytoplasm
- Extracellular
- Membrane
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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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| Not Available |
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Abnormal Concentrations |
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| Not Available |
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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 | FDB019173 |
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KNApSAcK ID | C00029439 |
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Chemspider ID | 24785442 |
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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 | 12901617 |
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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 | rw1878281 |
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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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