| 词条 | Trans-Resveratrol-3-O-glucuronide |
| 释义 |
| Verifiedfields = | verifiedrevid = | Name = trans-Resveratrol-3-O-glucuronide | ImageFile = Resveratrol 3-O-D-glucuronide.svg | ImageSize = | IUPACName = (2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[3-hydroxy-5-[(E)-2-(4-hydroxyphenyl)ethenyl]phenoxy]oxane-2-carboxylic acid | OtherNames = |Section1={{Chembox Identifiers | Abbreviations = | CASNo_Ref = | CASNo = 387372-17-0 | EINECS = | ChEMBL_Ref = | ChEMBL = | PubChem = 5273285 | ChemSpiderID = 4437760 | SMILES = O=C(O)[C@H]3O[C@@H](Oc2cc(O)cc(\\C=C\\c1ccc(O)cc1)c2)[C@H](O)[C@@H](O)[C@@H]3O | InChI = 1/C20H20O9/c21-12-5-3-10(4-6-12)1-2-11-7-13(22)9-14(8-11)28-20-17(25)15(23)16(24)18(29-20)19(26)27/h1-9,15-18,20-25H,(H,26,27)/b2-1+/t15-,16-,17+,18-,20+/m0/s1 | InChIKey = QWSAYEBSTMCFKY-OTPOQTMVBZ | StdInChI = 1S/C20H20O9/c21-12-5-3-10(4-6-12)1-2-11-7-13(22)9-14(8-11)28-20-17(25)15(23)16(24)18(29-20)19(26)27/h1-9,15-18,20-25H,(H,26,27)/b2-1+/t15-,16-,17+,18-,20+/m0/s1 | StdInChIKey = QWSAYEBSTMCFKY-OTPOQTMVSA-N | UNII_Ref = | UNII = | RTECS = | MeSHName = | ChEBI_Ref = | ChEBI = | KEGG_Ref = | KEGG = }} |Section2={{Chembox Properties | C=20 | H=20 | O=9 | Appearance = | Density = | MeltingPt = | MeltingPt_notes = | BoilingPt = | BoilingPt_notes = | Solubility = | SolubleOther = | Solvent = | pKa = | pKb = |Section7={{Chembox Hazards | EUClass = | MainHazards = | NFPA-H = | NFPA-F = | NFPA-R = | NFPA-S = | RPhrases = | SPhrases = | RSPhrases = | FlashPt = | AutoignitionPt = | ExploLimits = | PEL = }}trans-Resveratrol-3-O-glucuronide is a metabolite of resveratrol[1] and trans-resveratrol-3-O-glucoside (piceid).[2][3] References1. ^{{Cite journal | last1 = Urpi-Sarda | first1 = M. | last2 = Zamora-Ros | first2 = R. | last3 = Lamuela-Raventos | first3 = R. | last4 = Cherubini | first4 = A. | last5 = Jauregui | first5 = O. | last6 = De La Torre | first6 = R. | last7 = Covas | first7 = M. I. | last8 = Estruch | first8 = R. | last9 = Jaeger | first9 = W. | doi = 10.1373/clinchem.2006.071936 | last10 = Andres-Lacueva | first10 = C. | title = HPLC-Tandem Mass Spectrometric Method to Characterize Resveratrol Metabolism in Humans | journal = Clinical Chemistry | volume = 53 | issue = 2 | pages = 292–299 | year = 2006 | pmid = 17170057| pmc = }} {{Stilbenes}}{{DEFAULTSORT:Resveratrol-3-O-glucuronide, trans-}}{{Natural phenol-stub}}2. ^{{Cite journal | last1 = Zhou | first1 = M. | last2 = Chen | first2 = X. | last3 = Zhong | first3 = D. | title = Simultaneous determination of trans-resveratrol-3-O-glucoside and its two metabolites in rat plasma using liquid chromatography with ultraviolet detection | doi = 10.1016/j.jchromb.2007.04.025 | journal = Journal of Chromatography B | volume = 854 | pages = 219 | year = 2007 | pmid = | pmc = }} 3. ^{{Cite journal | last1 = Mikulski | first1 = D. | last2 = Molski | first2 = M. | doi = 10.1016/j.ejmech.2010.02.016 | title = Quantitative structure–antioxidant activity relationship of trans-resveratrol oligomers, trans-4,4′-dihydroxystilbene dimer, trans-resveratrol-3-O-glucuronide, glucosides: Trans-piceid, cis-piceid, trans-astringin and trans-resveratrol-4′-O-β-D-glucopyranoside | journal = European Journal of Medicinal Chemistry | volume = 45 | issue = 6 | pages = 2366–2380 | year = 2010 | pmid = 20199826 | pmc = }} 3 : Resveratrol glycosides|Phenol glucuronides|Phenolic human metabolites |
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