Main compound image
(2s,3s,4s,5r)-3,4,5-trihydroxy-6-[3-hydroxy-4-oxo-2-(3,4,5-trimethoxyphenyl)chromen-7-yl]oxyoxane-2-carboxylic acid
  • Other Name: (2S,3S,4S,5R)-3,4,5-trihydroxy-6-[3-hydroxy-4-oxo-2-(3,4,5-trimethoxyphenyl)chromen-7-yl]oxyoxane-2-carboxylic acid
  • InChIKey: YYBBCDHBDWPAKT-ZTCBVEBZSA-N
  • InChI: InChI=1S/C24H24O13/c1-32-13-6-9(7-14(33-2)21(13)34-3)20-17(27)15(25)11-5-4-10(8-12(11)36-20)35-24-19(29)16(26)18(28)22(37-24)23(30)31/h4-8,16,18-19,22,24,26-29H,1-3H3,(H,30,31)/t16-,18-,19+,22-,24?/m0/s1
  • SMILES: COC1=CC(=CC(=C1OC)OC)C2=C(C(=O)C3=C(O2)C=C(C=C3)OC4[C@@H]([C@H]([C@@H]([C@H](O4)C(=O)O)O)O)O)O
  • Exact Mass: 520.12169
  • Molecular Formula: C24H24O13
  • Compound CID: pubchemlite154700128 pubchem154700128
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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