| 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 18:37:10 UTC |
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| Update Date | 2022-03-07 02:53:52 UTC |
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| HMDB ID | HMDB0033846 |
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| Secondary Accession Numbers | |
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| Metabolite Identification |
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| Common Name | Corchoroside A |
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| Description | Corchoroside A belongs to the class of organic compounds known as cardenolide glycosides and derivatives. Cardenolide glycosides and derivatives are compounds containing a carbohydrate glycosidically bound to the cardenolide moiety. Based on a literature review a significant number of articles have been published on Corchoroside A. |
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| Structure | CC1OC(CC(O)C1O)OC1CCC2(C=O)C3CCC4(C)C(CCC4(O)C3CCC2(O)C1)C1=CC(=O)OC1 InChI=1S/C29H42O9/c1-16-25(33)22(31)12-24(37-16)38-18-3-8-27(15-30)20-4-7-26(2)19(17-11-23(32)36-14-17)6-10-29(26,35)21(20)5-9-28(27,34)13-18/h11,15-16,18-22,24-25,31,33-35H,3-10,12-14H2,1-2H3 |
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| Synonyms | | Value | Source |
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| Corchorosid a | HMDB | | Corchorozide a | HMDB | | Deglucoerysimoside | HMDB | | Erizimin | HMDB | | Erysimin | HMDB | | Helvetikosid | HMDB | | Korchoroside a | HMDB | | Strophanthidin 3-beta-digitoxoside | HMDB | | Strophanthidin boivinoside | HMDB | | Strophanthidin-beta-D-digitoxosid | HMDB | | Corchoroside a | MeSH |
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| Chemical Formula | C29H42O9 |
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| Average Molecular Weight | 534.6384 |
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| Monoisotopic Molecular Weight | 534.282882942 |
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| IUPAC Name | 5-[(4,5-dihydroxy-6-methyloxan-2-yl)oxy]-7,11-dihydroxy-15-methyl-14-(5-oxo-2,5-dihydrofuran-3-yl)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecane-2-carbaldehyde |
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| Traditional Name | 5-[(4,5-dihydroxy-6-methyloxan-2-yl)oxy]-7,11-dihydroxy-15-methyl-14-(5-oxo-2H-furan-3-yl)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecane-2-carbaldehyde |
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| CAS Registry Number | 508-76-9 |
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| SMILES | CC1OC(CC(O)C1O)OC1CCC2(C=O)C3CCC4(C)C(CCC4(O)C3CCC2(O)C1)C1=CC(=O)OC1 |
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| InChI Identifier | InChI=1S/C29H42O9/c1-16-25(33)22(31)12-24(37-16)38-18-3-8-27(15-30)20-4-7-26(2)19(17-11-23(32)36-14-17)6-10-29(26,35)21(20)5-9-28(27,34)13-18/h11,15-16,18-22,24-25,31,33-35H,3-10,12-14H2,1-2H3 |
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| InChI Key | QBILRDAMJUPXCX-UHFFFAOYSA-N |
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| Chemical Taxonomy |
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| Description | Belongs to the class of organic compounds known as cardenolide glycosides and derivatives. Cardenolide glycosides and derivatives are compounds containing a carbohydrate glycosidically bound to the cardenolide moiety. |
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| Kingdom | Organic compounds |
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| Super Class | Lipids and lipid-like molecules |
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| Class | Steroids and steroid derivatives |
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| Sub Class | Steroid lactones |
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| Direct Parent | Cardenolide glycosides and derivatives |
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| Alternative Parents | |
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| Substituents | - Cardanolide-glycoside
- Steroidal glycoside
- 19-oxosteroid
- 14-hydroxysteroid
- 5-hydroxysteroid
- Hydroxysteroid
- Oxosteroid
- Hexose monosaccharide
- Glycosyl compound
- O-glycosyl compound
- 2-furanone
- Monosaccharide
- Oxane
- Cyclic alcohol
- Dihydrofuran
- Alpha,beta-unsaturated carboxylic ester
- Enoate ester
- Tertiary alcohol
- Carboxylic acid ester
- Lactone
- Secondary alcohol
- Organoheterocyclic compound
- Oxacycle
- Acetal
- Carboxylic acid derivative
- Monocarboxylic acid or derivatives
- Aldehyde
- Hydrocarbon derivative
- Alcohol
- Organic oxide
- Carbonyl group
- Organic oxygen compound
- Organooxygen compound
- Aliphatic heteropolycyclic compound
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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 | 188 - 190 °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 Retention Times Underivatized| Chromatographic Method | Retention Time | Reference |
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| Measured using a Waters Acquity ultraperformance liquid chromatography (UPLC) ethylene-bridged hybrid (BEH) C18 column (100 mm × 2.1 mm; 1.7 μmparticle diameter). Predicted by Afia on May 17, 2022. Predicted by Afia on May 17, 2022. | 6.34 minutes | 32390414 | | Predicted by Siyang on May 30, 2022 | 13.1245 minutes | 33406817 | | Predicted by Siyang using ReTip algorithm on June 8, 2022 | 2.44 minutes | 32390414 | | Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid | 3006.9 seconds | 40023050 | | Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid | 161.5 seconds | 40023050 | | Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid | 204.6 seconds | 40023050 | | Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid | 165.9 seconds | 40023050 | | RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid | 187.0 seconds | 40023050 | | Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid | 597.0 seconds | 40023050 | | BfG_NTS_RP1 =Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) with Water:ACN and 0.1% Formic Acid | 611.6 seconds | 40023050 | | HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate) | 130.0 seconds | 40023050 | | UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid | 1103.3 seconds | 40023050 | | BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid | 491.1 seconds | 40023050 | | UFZ_Phenomenex = Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex with Water:MeOH and 0.1% Formic Acid | 1589.1 seconds | 40023050 | | SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid | 376.9 seconds | 40023050 | | RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid | 397.3 seconds | 40023050 | | MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate | 292.5 seconds | 40023050 | | KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA | 236.4 seconds | 40023050 | | Meister zic-pHILIC pH9.3 = Merck SeQuant ZIC-pHILIC column with ACN:Water 5mM NH4Ac pH9.3 and 5mM ammonium acetate in water | 74.6 seconds | 40023050 |
Predicted Kovats Retention IndicesUnderivatizedDerivatized| Derivative Name / Structure | SMILES | Kovats RI Value | Column Type | Reference |
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| Corchoroside A,1TMS,isomer #1 | CC1OC(OC2CCC3(C=O)C4CCC5(C)C(C6=CC(=O)OC6)CCC5(O)C4CCC3(O)C2)CC(O[Si](C)(C)C)C1O | 4636.5 | Semi standard non polar | 33892256 | | Corchoroside A,1TMS,isomer #2 | CC1OC(OC2CCC3(C=O)C4CCC5(C)C(C6=CC(=O)OC6)CCC5(O)C4CCC3(O)C2)CC(O)C1O[Si](C)(C)C | 4652.7 | Semi standard non polar | 33892256 | | Corchoroside A,1TMS,isomer #3 | CC1OC(OC2CCC3(C=O)C4CCC5(C)C(C6=CC(=O)OC6)CCC5(O[Si](C)(C)C)C4CCC3(O)C2)CC(O)C1O | 4659.1 | Semi standard non polar | 33892256 | | Corchoroside A,1TMS,isomer #4 | CC1OC(OC2CCC3(C=O)C4CCC5(C)C(C6=CC(=O)OC6)CCC5(O)C4CCC3(O[Si](C)(C)C)C2)CC(O)C1O | 4631.5 | Semi standard non polar | 33892256 | | Corchoroside A,2TMS,isomer #1 | CC1OC(OC2CCC3(C=O)C4CCC5(C)C(C6=CC(=O)OC6)CCC5(O[Si](C)(C)C)C4CCC3(O)C2)CC(O[Si](C)(C)C)C1O | 4584.5 | Semi standard non polar | 33892256 | | Corchoroside A,2TMS,isomer #2 | CC1OC(OC2CCC3(C=O)C4CCC5(C)C(C6=CC(=O)OC6)CCC5(O)C4CCC3(O[Si](C)(C)C)C2)CC(O[Si](C)(C)C)C1O | 4573.8 | Semi standard non polar | 33892256 | | Corchoroside A,2TMS,isomer #3 | CC1OC(OC2CCC3(C=O)C4CCC5(C)C(C6=CC(=O)OC6)CCC5(O)C4CCC3(O)C2)CC(O[Si](C)(C)C)C1O[Si](C)(C)C | 4606.7 | Semi standard non polar | 33892256 | | Corchoroside A,2TMS,isomer #4 | CC1OC(OC2CCC3(C=O)C4CCC5(C)C(C6=CC(=O)OC6)CCC5(O[Si](C)(C)C)C4CCC3(O)C2)CC(O)C1O[Si](C)(C)C | 4620.5 | Semi standard non polar | 33892256 | | Corchoroside A,2TMS,isomer #5 | CC1OC(OC2CCC3(C=O)C4CCC5(C)C(C6=CC(=O)OC6)CCC5(O)C4CCC3(O[Si](C)(C)C)C2)CC(O)C1O[Si](C)(C)C | 4602.6 | Semi standard non polar | 33892256 | | Corchoroside A,2TMS,isomer #6 | CC1OC(OC2CCC3(C=O)C4CCC5(C)C(C6=CC(=O)OC6)CCC5(O[Si](C)(C)C)C4CCC3(O[Si](C)(C)C)C2)CC(O)C1O | 4606.3 | Semi standard non polar | 33892256 | | Corchoroside A,3TMS,isomer #1 | CC1OC(OC2CCC3(C=O)C4CCC5(C)C(C6=CC(=O)OC6)CCC5(O[Si](C)(C)C)C4CCC3(O[Si](C)(C)C)C2)CC(O[Si](C)(C)C)C1O | 4425.5 | Semi standard non polar | 33892256 | | Corchoroside A,3TMS,isomer #2 | CC1OC(OC2CCC3(C=O)C4CCC5(C)C(C6=CC(=O)OC6)CCC5(O[Si](C)(C)C)C4CCC3(O)C2)CC(O[Si](C)(C)C)C1O[Si](C)(C)C | 4486.6 | Semi standard non polar | 33892256 | | Corchoroside A,3TMS,isomer #3 | CC1OC(OC2CCC3(C=O)C4CCC5(C)C(C6=CC(=O)OC6)CCC5(O)C4CCC3(O[Si](C)(C)C)C2)CC(O[Si](C)(C)C)C1O[Si](C)(C)C | 4496.9 | Semi standard non polar | 33892256 | | Corchoroside A,3TMS,isomer #4 | CC1OC(OC2CCC3(C=O)C4CCC5(C)C(C6=CC(=O)OC6)CCC5(O[Si](C)(C)C)C4CCC3(O[Si](C)(C)C)C2)CC(O)C1O[Si](C)(C)C | 4483.3 | Semi standard non polar | 33892256 | | Corchoroside A,4TMS,isomer #1 | CC1OC(OC2CCC3(C=O)C4CCC5(C)C(C6=CC(=O)OC6)CCC5(O[Si](C)(C)C)C4CCC3(O[Si](C)(C)C)C2)CC(O[Si](C)(C)C)C1O[Si](C)(C)C | 4325.1 | Semi standard non polar | 33892256 | | Corchoroside A,1TBDMS,isomer #1 | CC1OC(OC2CCC3(C=O)C4CCC5(C)C(C6=CC(=O)OC6)CCC5(O)C4CCC3(O)C2)CC(O[Si](C)(C)C(C)(C)C)C1O | 4863.7 | Semi standard non polar | 33892256 | | Corchoroside A,1TBDMS,isomer #2 | CC1OC(OC2CCC3(C=O)C4CCC5(C)C(C6=CC(=O)OC6)CCC5(O)C4CCC3(O)C2)CC(O)C1O[Si](C)(C)C(C)(C)C | 4889.4 | Semi standard non polar | 33892256 | | Corchoroside A,1TBDMS,isomer #3 | CC1OC(OC2CCC3(C=O)C4CCC5(C)C(C6=CC(=O)OC6)CCC5(O[Si](C)(C)C(C)(C)C)C4CCC3(O)C2)CC(O)C1O | 4867.7 | Semi standard non polar | 33892256 | | Corchoroside A,1TBDMS,isomer #4 | CC1OC(OC2CCC3(C=O)C4CCC5(C)C(C6=CC(=O)OC6)CCC5(O)C4CCC3(O[Si](C)(C)C(C)(C)C)C2)CC(O)C1O | 4844.6 | Semi standard non polar | 33892256 | | Corchoroside A,2TBDMS,isomer #1 | CC1OC(OC2CCC3(C=O)C4CCC5(C)C(C6=CC(=O)OC6)CCC5(O[Si](C)(C)C(C)(C)C)C4CCC3(O)C2)CC(O[Si](C)(C)C(C)(C)C)C1O | 5002.2 | Semi standard non polar | 33892256 | | Corchoroside A,2TBDMS,isomer #2 | CC1OC(OC2CCC3(C=O)C4CCC5(C)C(C6=CC(=O)OC6)CCC5(O)C4CCC3(O[Si](C)(C)C(C)(C)C)C2)CC(O[Si](C)(C)C(C)(C)C)C1O | 4991.3 | Semi standard non polar | 33892256 | | Corchoroside A,2TBDMS,isomer #3 | CC1OC(OC2CCC3(C=O)C4CCC5(C)C(C6=CC(=O)OC6)CCC5(O)C4CCC3(O)C2)CC(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C | 5043.9 | Semi standard non polar | 33892256 | | Corchoroside A,2TBDMS,isomer #4 | CC1OC(OC2CCC3(C=O)C4CCC5(C)C(C6=CC(=O)OC6)CCC5(O[Si](C)(C)C(C)(C)C)C4CCC3(O)C2)CC(O)C1O[Si](C)(C)C(C)(C)C | 5044.8 | Semi standard non polar | 33892256 | | Corchoroside A,2TBDMS,isomer #5 | CC1OC(OC2CCC3(C=O)C4CCC5(C)C(C6=CC(=O)OC6)CCC5(O)C4CCC3(O[Si](C)(C)C(C)(C)C)C2)CC(O)C1O[Si](C)(C)C(C)(C)C | 5030.0 | Semi standard non polar | 33892256 | | Corchoroside A,2TBDMS,isomer #6 | CC1OC(OC2CCC3(C=O)C4CCC5(C)C(C6=CC(=O)OC6)CCC5(O[Si](C)(C)C(C)(C)C)C4CCC3(O[Si](C)(C)C(C)(C)C)C2)CC(O)C1O | 5020.3 | Semi standard non polar | 33892256 | | Corchoroside A,3TBDMS,isomer #1 | CC1OC(OC2CCC3(C=O)C4CCC5(C)C(C6=CC(=O)OC6)CCC5(O[Si](C)(C)C(C)(C)C)C4CCC3(O[Si](C)(C)C(C)(C)C)C2)CC(O[Si](C)(C)C(C)(C)C)C1O | 5077.2 | Semi standard non polar | 33892256 | | Corchoroside A,3TBDMS,isomer #2 | CC1OC(OC2CCC3(C=O)C4CCC5(C)C(C6=CC(=O)OC6)CCC5(O[Si](C)(C)C(C)(C)C)C4CCC3(O)C2)CC(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C | 5107.2 | Semi standard non polar | 33892256 | | Corchoroside A,3TBDMS,isomer #3 | CC1OC(OC2CCC3(C=O)C4CCC5(C)C(C6=CC(=O)OC6)CCC5(O)C4CCC3(O[Si](C)(C)C(C)(C)C)C2)CC(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C | 5127.6 | Semi standard non polar | 33892256 | | Corchoroside A,3TBDMS,isomer #4 | CC1OC(OC2CCC3(C=O)C4CCC5(C)C(C6=CC(=O)OC6)CCC5(O[Si](C)(C)C(C)(C)C)C4CCC3(O[Si](C)(C)C(C)(C)C)C2)CC(O)C1O[Si](C)(C)C(C)(C)C | 5127.8 | Semi standard non polar | 33892256 |
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| GC-MS Spectra| Spectrum Type | Description | Splash Key | Deposition Date | Source | View |
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| Predicted GC-MS | Predicted GC-MS Spectrum - Corchoroside A GC-MS (Non-derivatized) - 70eV, Positive | splash10-0a4i-3428290000-5c4f64d4b14e2fd7b013 | 2017-09-01 | Wishart Lab | View Spectrum | | Predicted GC-MS | Predicted GC-MS Spectrum - Corchoroside A GC-MS (2 TMS) - 70eV, Positive | splash10-0j4i-4232709000-9d18189de6b042461571 | 2017-10-06 | Wishart Lab | View Spectrum | | Predicted GC-MS | Predicted GC-MS Spectrum - Corchoroside A GC-MS (TMS_1_1) - 70eV, Positive | Not Available | 2021-10-13 | Wishart Lab | View Spectrum | | Predicted GC-MS | Predicted GC-MS Spectrum - Corchoroside A GC-MS (TMS_1_2) - 70eV, Positive | Not Available | 2021-10-13 | Wishart Lab | View Spectrum | | Predicted GC-MS | Predicted GC-MS Spectrum - Corchoroside A GC-MS (TMS_1_3) - 70eV, Positive | Not Available | 2021-10-13 | Wishart Lab | View Spectrum | | Predicted GC-MS | Predicted GC-MS Spectrum - Corchoroside A GC-MS (TMS_1_4) - 70eV, Positive | Not Available | 2021-10-13 | Wishart Lab | View Spectrum | | Predicted GC-MS | Predicted GC-MS Spectrum - Corchoroside A GC-MS (TMS_2_2) - 70eV, Positive | Not Available | 2021-10-13 | Wishart Lab | View Spectrum | | Predicted GC-MS | Predicted GC-MS Spectrum - Corchoroside A GC-MS (TMS_2_3) - 70eV, Positive | Not Available | 2021-10-13 | Wishart Lab | View Spectrum | | Predicted GC-MS | Predicted GC-MS Spectrum - Corchoroside A GC-MS (TMS_2_4) - 70eV, Positive | Not Available | 2021-10-13 | Wishart Lab | View Spectrum | | Predicted GC-MS | Predicted GC-MS Spectrum - Corchoroside A GC-MS (TMS_2_5) - 70eV, Positive | Not Available | 2021-10-13 | Wishart Lab | View Spectrum | | Predicted GC-MS | Predicted GC-MS Spectrum - Corchoroside A GC-MS (TMS_2_6) - 70eV, Positive | Not Available | 2021-10-13 | Wishart Lab | View Spectrum | | Predicted GC-MS | Predicted GC-MS Spectrum - Corchoroside A GC-MS (TMS_3_1) - 70eV, Positive | Not Available | 2021-10-13 | Wishart Lab | View Spectrum | | Predicted GC-MS | Predicted GC-MS Spectrum - Corchoroside A GC-MS (TMS_3_2) - 70eV, Positive | Not Available | 2021-10-13 | Wishart Lab | View Spectrum | | Predicted GC-MS | Predicted GC-MS Spectrum - Corchoroside A GC-MS (TMS_3_3) - 70eV, Positive | Not Available | 2021-10-13 | Wishart Lab | View Spectrum | | Predicted GC-MS | Predicted GC-MS Spectrum - Corchoroside A GC-MS (TMS_3_4) - 70eV, Positive | Not Available | 2021-10-13 | Wishart Lab | View Spectrum | | Predicted GC-MS | Predicted GC-MS Spectrum - Corchoroside A GC-MS (TMS_4_1) - 70eV, Positive | Not Available | 2021-10-13 | Wishart Lab | View Spectrum | | Predicted GC-MS | Predicted GC-MS Spectrum - Corchoroside A GC-MS (TBDMS_1_1) - 70eV, Positive | Not Available | 2021-10-13 | Wishart Lab | View Spectrum | | Predicted GC-MS | Predicted GC-MS Spectrum - Corchoroside A GC-MS (TBDMS_1_2) - 70eV, Positive | Not Available | 2021-10-13 | Wishart Lab | View Spectrum | | Predicted GC-MS | Predicted GC-MS Spectrum - Corchoroside A GC-MS (TBDMS_1_3) - 70eV, Positive | Not Available | 2021-10-13 | Wishart Lab | View Spectrum | | Predicted GC-MS | Predicted GC-MS Spectrum - Corchoroside A GC-MS (TBDMS_1_4) - 70eV, Positive | Not Available | 2021-10-13 | Wishart Lab | View Spectrum | | Predicted GC-MS | Predicted GC-MS Spectrum - Corchoroside A GC-MS (TBDMS_2_1) - 70eV, Positive | Not Available | 2021-10-13 | Wishart Lab | View Spectrum | | Predicted GC-MS | Predicted GC-MS Spectrum - Corchoroside A GC-MS (TBDMS_2_2) - 70eV, Positive | Not Available | 2021-10-13 | Wishart Lab | View Spectrum | | Predicted GC-MS | Predicted GC-MS Spectrum - Corchoroside A GC-MS (TBDMS_2_3) - 70eV, Positive | Not Available | 2021-10-13 | Wishart Lab | View Spectrum | | Predicted GC-MS | Predicted GC-MS Spectrum - Corchoroside A GC-MS (TBDMS_2_4) - 70eV, Positive | Not Available | 2021-10-13 | Wishart Lab | View Spectrum | | Predicted GC-MS | Predicted GC-MS Spectrum - Corchoroside A GC-MS (TBDMS_2_5) - 70eV, Positive | Not Available | 2021-10-13 | Wishart Lab | View Spectrum |
MS/MS Spectra| Spectrum Type | Description | Splash Key | Deposition Date | Source | View |
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| Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Corchoroside A 10V, Positive-QTOF | splash10-0671-0005960000-f6c491c1afb376afc934 | 2015-04-24 | Wishart Lab | View Spectrum | | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Corchoroside A 20V, Positive-QTOF | splash10-000i-0209310000-5febbf49bfef9e39a999 | 2015-04-24 | Wishart Lab | View Spectrum | | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Corchoroside A 40V, Positive-QTOF | splash10-000i-2459200000-a3514d0b4377a427aa50 | 2015-04-24 | Wishart Lab | View Spectrum | | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Corchoroside A 10V, Positive-QTOF | splash10-0671-0005960000-f6c491c1afb376afc934 | 2015-04-24 | Wishart Lab | View Spectrum | | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Corchoroside A 20V, Positive-QTOF | splash10-000i-0209310000-5febbf49bfef9e39a999 | 2015-04-24 | Wishart Lab | View Spectrum | | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Corchoroside A 40V, Positive-QTOF | splash10-000i-2459200000-a3514d0b4377a427aa50 | 2015-04-24 | Wishart Lab | View Spectrum | | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Corchoroside A 10V, Negative-QTOF | splash10-001r-0103490000-b45a0c95d8af75758037 | 2015-04-25 | Wishart Lab | View Spectrum | | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Corchoroside A 20V, Negative-QTOF | splash10-0f9i-1105920000-73d79a1f0deac0c59d43 | 2015-04-25 | Wishart Lab | View Spectrum | | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Corchoroside A 40V, Negative-QTOF | splash10-0udr-4009600000-c29de620e8b1286cd955 | 2015-04-25 | Wishart Lab | View Spectrum | | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Corchoroside A 10V, Negative-QTOF | splash10-001r-0103490000-b45a0c95d8af75758037 | 2015-04-25 | Wishart Lab | View Spectrum | | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Corchoroside A 20V, Negative-QTOF | splash10-0f9i-1105920000-73d79a1f0deac0c59d43 | 2015-04-25 | Wishart Lab | View Spectrum | | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Corchoroside A 40V, Negative-QTOF | splash10-0udr-4009600000-c29de620e8b1286cd955 | 2015-04-25 | Wishart Lab | View Spectrum | | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Corchoroside A 10V, Positive-QTOF | splash10-000i-0009760000-356a5208f6f65032264c | 2021-09-22 | Wishart Lab | View Spectrum | | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Corchoroside A 20V, Positive-QTOF | splash10-000i-0203920000-ba2d7e5a7d5fd3662880 | 2021-09-22 | Wishart Lab | View Spectrum | | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Corchoroside A 40V, Positive-QTOF | splash10-07cs-4942500000-cd94c1a143f714823dd2 | 2021-09-22 | Wishart Lab | View Spectrum | | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Corchoroside A 10V, Negative-QTOF | splash10-001i-0001490000-313a14e623bcc56af4f1 | 2021-09-23 | Wishart Lab | View Spectrum | | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Corchoroside A 20V, Negative-QTOF | splash10-0059-0002950000-4798868455af007aa8b8 | 2021-09-23 | Wishart Lab | View Spectrum | | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Corchoroside A 40V, Negative-QTOF | splash10-002f-9203610000-1e2c55f045256e60186d | 2021-09-23 | Wishart Lab | View Spectrum |
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