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Fig. A, 1H NMR spectra (400 MHz) for: (a) MeO-PEGN-SuccOH; (b) the resveratrol-PEG conjugate mixture from the synthesis of MeO-PEGN-Succ-RSV; (c) resveratrol; and (d) the solution from (b) after treatment with water and heat (90°C) for ca. 1 week).

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Figshare2015-12-03 更新2026-04-29 收录
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https://figshare.com/articles/dataset/_Stabilization_of_Resveratrol_in_Blood_Circulation_by_Conjugation_to_mPEG_and_mPEG_PLA_Polymers_Investigation_of_Conjugate_Linker_and_Polymer_Composition_on_Stability_Metabolism_Antioxidant_Activity_and_Pharmacokinetic_Profile_/1350029
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All solutions are in d6-DMSO. Key: † = d5-DMSO, ‡ = H2O. To identify the low intensity down-field signals the spectra in (a), (b) and (d) have been expanded vertically. Fig. B, The down field region of the 1H NMR spectra (400 MHz) for: (a) a solution of the resveratrol-PEG conjugate mixture in d6-DMSO showing the assigned signals for the two major products 4'-MeO-PEGN-Succ-RSV and 3-MeO-PEGN-Succ—RSV; and (b) a solution of resveratrol in d6-DMSO. Fig. C, 1H NMR spectra for the MeO-PEGN-Succ-RSV conjugate mixture in d6-DMSO, recorded at 400 MHz. Key: † = d5-DMSO, ‡ = H2O. Fig. D, 1H NMR spectra for MeO-PEGN-Succ-OH in d6-DMSO, recorded at 400 MHz. Key: † = d5-DMSO, ‡ = H2O. Fig. E, 1H NMR spectra of the MeO-PEGN-Succ-RSV conjugate mixture after treatment with water and heat (90°C) for ca. 1 week, in d6-DMSO, recorded at 400 MHz. Key: † = d5-DMSO, ‡ = H2O. (DOCX)
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2015-12-03
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