Main compound image
(2s,3s,4s,5r)-3,4,5-trihydroxy-6-[(4,6,6-trimethyl-5-oxo-2-bicyclo[2.2.1]heptanyl)oxy]oxane-2-carboxylic acid
  • Other Name: (2S,3S,4S,5R)-3,4,5-trihydroxy-6-[(4,6,6-trimethyl-5-oxo-2-bicyclo[2.2.1]heptanyl)oxy]oxane-2-carboxylic acid
  • InChIKey: OVBFDDZQQOCVTB-NJPGAIFGSA-N
  • InChI: InChI=1S/C16H24O8/c1-15(2)6-4-16(3,14(15)22)5-7(6)23-13-10(19)8(17)9(18)11(24-13)12(20)21/h6-11,13,17-19H,4-5H2,1-3H3,(H,20,21)/t6?,7?,8-,9-,10+,11-,13?,16?/m0/s1
  • SMILES: CC1(C2CC(C1=O)(CC2OC3[C@@H]([C@H]([C@@H]([C@H](O3)C(=O)O)O)O)O)C)C
  • Exact Mass: 344.14712
  • Molecular Formula: C16H24O8
  • Compound CID: pubchemlite154699865 pubchem154699865
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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