Three-Dimensional Quantitative Structure-Activity Relationship Studies on UGT1A9-Mediated 3-O-Glucuronidation of Natural Flavonols Using a Pharmacophore-Based Comparative Molecular Field Analysis Model

Data Supplement

Files in this Data Supplement:

• Data Supplement -
  Table S1. The conversion factors (K) are showed at detecting wavelengths for flavonol 3-O-glucuronides.
  Figure S1. Characterization on the recombinant UGT1A9 using the probe substrate "propofol"...
  Figure S2. The UPLC chromatograms (left panel) and UV spectra (right panel) of multi-hydroxyl flavonols and their 3-O-glucuronides...
  Figure.S3 Kinetics profiles of UGT1A9 with 26 flavonols (3-O-glucuronidation alone)...