Main compound image
9-epiallogibberic acid
  • Other Name: (4bR,7S,9aS,10R)-7-Hydroxy-1-methyl-8-methylene-5,6,7,8,9,10-hexahydro-4bH-7,9a-methanobenzo[a]azulene-10-carboxylic acid
  • InChIKey: IFYWTLQMNWNCFH-DHXZDTOLSA-N
  • InChI: InChI=1S/C18H20O3/c1-10-4-3-5-12-13-6-7-18(21)9-17(13,8-11(18)2)15(14(10)12)16(19)20/h3-5,13,15,21H,2,6-9H2,1H3,(H,19,20)/t13-,15+,17-,18-/m0/s1
  • SMILES: CC1=C2[C@@H]([C@@]34CC(=C)[C@@](C3)(CC[C@H]4C2=CC=C1)O)C(=O)O
  • Exact Mass: 284.14124
  • Molecular Formula: C18H20O3
  • Compound CID: pubchemlite12305929 pubchem12305929
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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