3-O-Glukuronid trans-resweratrolu
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| Nazewnictwo
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| Nomenklatura systematyczna (IUPAC)
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kwas (2S,3S,4S,5R,6S)-3,4,5-trihydroksy-6-[3-hydroksy-5-[(E)-2-(4-hydroksyfenylo)etenylo]fenoksy]oksano-2-karboksylowy
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| Ogólne informacje
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| Wzór sumaryczny
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C20H20O9
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| Masa molowa
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404,37 g/mol
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| Identyfikacja
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| Numer CAS
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387372-17-0
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| PubChem
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5273285
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| SMILES
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C1=CC(=CC=C1C=CC2=CC(=CC(=C2)OC3C(C(C(C(O3)C(=O)O)O)O)O)O)O
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| InChI
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InChI=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
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| InChIKey
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QWSAYEBSTMCFKY-OTPOQTMVSA-N
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3-O-Glukuronid trans-resweratrolu – organiczny związek chemiczny, metabolit resweratrolu[1] i 3-O-glukozydu trans-resweratrolu[2][3].
- ↑ MireiaM. Urpi-Sarda MireiaM. i inni, HPLC–Tandem Mass Spectrometric Method to Characterize Resveratrol Metabolism in Humans, „Clinical Chemistry”, 53 (2), 2007, s. 292–299, DOI: 10.1373/clinchem.2006.071936 .
- ↑ MaojinM. Zhou MaojinM., XiaoyanX. Chen XiaoyanX., DafangD. Zhong DafangD., Simultaneous determination of trans-resveratrol-3-O-glucoside and its two metabolites in rat plasma using liquid chromatography with ultraviolet detection, „Journal of Chromatography B”, 854 (1–2), 2007, s. 219–223, DOI: 10.1016/j.jchromb.2007.04.025 .
- ↑ DamianD. Mikulski DamianD., MarcinM. Molski MarcinM., 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-beta-D-glucopyranoside, „European Journal of Medicinal Chemistry”, 45 (6), 2010, s. 2366–2380, DOI: 10.1016/j.ejmech.2010.02.016 .
