Main compound image
Diosmin metabolite i
  • InChIKey: JYIYMIHKVQPEDW-GPAYOWEBSA-N
  • InChI: InChI=1S/C27H32O14/c1-10-20(30)22(32)24(34)26(38-10)37-9-19-21(31)23(33)25(35)27(41-19)39-12-6-14(28)13-8-17(40-18(13)7-12)11-3-4-16(36-2)15(29)5-11/h3-8,10,19-35H,9H2,1-2H3/t10-,19+,20-,21+,22+,23-,24+,25+,26+,27+/m0/s1
  • SMILES: C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)OC[C@@H]2[C@H]([C@@H]([C@H]([C@@H](O2)OC3=CC(=C4C=C(OC4=C3)C5=CC(=C(C=C5)OC)O)O)O)O)O)O)O)O
  • Exact Mass: 580.17921
  • Molecular Formula: C27H32O14
  • Compound CID: pubchemlite169501944 pubchem169501944
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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