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  1. www.researchgate.net › publication › 230111088_Two_New_Resveratrol_5-1E-2-4Two New Resveratrol...

    27 Φεβ 2004 · The structures of 1 and 2 composed of four resveratrol (=5- [ (1E)-2- (4-hydroxyphenyl)ethenyl]benzene-1,3-diol) units had eight asymmetric C-atoms in the partial structures of a tetrahydrofuran...

  2. Molecular Formula. C28H22O6. Synonyms. (2R,3S)-trans-epsilon-viniferin. 5- [ (2R,3S)-6-hydroxy-2- (4-hydroxyphenyl)-4- [ (E)-2- (4-hydroxyphenyl)ethenyl]-2,3-dihydro-1-benzofuran-3-yl]benzene-1,3-diol. 5- { (2R,3S)-6-hydroxy-2- (4-hydroxyphenyl)-4- [ (E)-2- (4-hydroxyphenyl)ethenyl]-2,3-dihydro-1-benzofuran-3-yl}benzene-1,3-diol. CHEBI:76143.

  3. 14 Οκτ 2021 · 4- [ [2,4-dihydroxy-6- [ (E)-2- (4-hydroxyphenyl)ethenyl]phenyl]diazenyl]-5- [ (Z)-2- (4-hydroxyphenyl)ethenyl]benzene-1,3-diol | C28H22N2O6 | CID 136848744 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists, and more.

  4. www.semanticscholar.org › paper › Two-New-Resveratrol-(=-Tetramers-with-a-Ring-fromTwo New Resveratrol (=...

    1 Φεβ 2004 · Four new resveratrol derivatives are isolated from the stem of Hopea parviflora and have a common partial structure of the 1-hydroxy-1-(3,5-dihydroxy-2-C-glucopyranosylphenyl)-2-(4-hydroxyphenyl)ethane- 2-yl group after oxidative condensation of (E)-resveratroside.

  5. 13 Σεπ 2017 · 5-[2-(4-Hydroxyphenyl)ethenyl]-2-(3-methylbut-2-enoxy)benzene-1,3-diol | C19H20O4 | CID 129847915 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists, and more.

  6. Resveratrol (5-[(E)-2-(4-hydroxyphenyl)ethenyl]benzene-1,3-diol) is a dietary polyphenol, belonging to the stilbenes group and naturally occurring in fruits and food products (Bhat et al. 2001; Harikumar and Aggarwal 2008) and active dur-

  7. Data source: National Magnetic Resonance Facility at Madison - Maria Nesterova, Lawrence J. Clos, Christopher Stancic, Mark E. Anderson, John L. Markley NMR-STAR file : bmse001136.str