Main compound image
(2s,3s,4s,5r,6s)-3,4,5-trihydroxy-6-(4-(9-hydroxy-8-oxo-8h-[1,3]dioxolo[4,5-g]chromen-7-yl)phenoxy)tetrahydro-2h-pyran-2-carboxylic acid
  • Other Name: (2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[4-(9-hydroxy-8-oxo-[1,3]dioxolo[4,5-g]chromen-7-yl)phenoxy]oxane-2-carboxylic acid
  • InChIKey: LLPADQARYIBKIE-QSUZLTIMSA-N
  • InChI: InChI=1S/C22H18O12/c23-14-10(6-30-11-5-12-19(32-7-31-12)15(24)13(11)14)8-1-3-9(4-2-8)33-22-18(27)16(25)17(26)20(34-22)21(28)29/h1-6,16-18,20,22,24-27H,7H2,(H,28,29)/t16-,17-,18+,20-,22+/m0/s1
  • SMILES: C1OC2=C(O1)C(=C3C(=C2)OC=C(C3=O)C4=CC=C(C=C4)O[C@H]5[C@@H]([C@H]([C@@H]([C@H](O5)C(=O)O)O)O)O)O
  • Exact Mass: 474.07983
  • Molecular Formula: C22H18O12
  • Compound CID: pubchemlite118753334 pubchem118753334
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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