Main compound image
(-)-epigallocatechin gallate, 3p-hydroxy-glucuronide
  • Other Name: (2S,3S,4S,5R,6S)-6-[5-[(2R,3R)-5,7-dihydroxy-3-(3,4,5-trihydroxybenzoyl)oxy-3,4-dihydro-2H-chromen-2-yl]-2,3-dihydroxyphenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid
  • InChIKey: WNLLMSQFYPFJGS-ZCRVWPRHSA-N
  • InChI: InChI=1S/C28H26O17/c29-10-5-12(30)11-7-18(43-27(41)9-2-13(31)19(34)14(32)3-9)24(42-16(11)6-10)8-1-15(33)20(35)17(4-8)44-28-23(38)21(36)22(37)25(45-28)26(39)40/h1-6,18,21-25,28-38H,7H2,(H,39,40)/t18-,21+,22+,23-,24-,25+,28-/m1/s1
  • SMILES: C1[C@H]([C@H](OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)C(=O)O)O)O)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O
  • Exact Mass: 634.11700
  • Molecular Formula: C28H26O17
  • Compound CID: pubchemlite154700057 pubchem154700057
Hidden Reactions Filter Some biological reactions link very small precursors (e.g. CO₂, acetate) to much larger products. These reactions are correct, but they can create unrealistic shortest paths and connect otherwise separate parts of the graph. To keep the overview readable, FAIR-TPs hides six such reactions where a <60 Da precursor leads to a >300 Da product in the visualisations.

You can have all these paths in the download output.
Hidden reaction pairs (precursor → product):
  • Acetate → N-(2-benzoyl-4-chlorophenyl)-2-acetamidoacetamide
  • Acetate → N-(2-benzoyl-4-chlorophenyl)-2-acetamido-n-methylacetamide
  • Carbon dioxide → Formylmethanofuran
  • Acrolein → Chembl3706542
  • Ethylene oxide → Acetyl-coa
  • Formaldehyde → S-hydroxymethylglutathione
Note: In the graph output, up to 100 compounds are displayed for faster visualization. For the full output, please use the export files.

Click on a node or edge to see details here.

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