Main compound image
dibenzo[a,l]pyrene-12-ol, 11-o-glucuronide
  • Other Name: (2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[(19-hydroxy-18-hexacyclo[10.10.2.02,7.08,24.015,23.017,22]tetracosa-1(23),2,4,6,8,10,12(24),13,15,17(22),18,20-dodecaenyl)oxy]oxane-2-carboxylic acid
  • InChIKey: AQEIIITVYFRNER-ZLBJCVPKSA-N
  • InChI: InChI=1S/C30H22O8/c31-20-11-10-18-19(27(20)37-30-26(34)24(32)25(33)28(38-30)29(35)36)12-14-9-8-13-4-3-7-16-15-5-1-2-6-17(15)23(18)22(14)21(13)16/h1-12,24-26,28,30-34H,(H,35,36)/t24-,25-,26+,28-,30+/m0/s1
  • SMILES: C1=CC=C2C(=C1)C3=CC=CC4=C3C5=C2C6=C(C=C5C=C4)C(=C(C=C6)O)O[C@H]7[C@@H]([C@H]([C@@H]([C@H](O7)C(=O)O)O)O)O
  • Exact Mass: 510.13147
  • Molecular Formula: C30H22O8
  • Compound CID: pubchemlite154699486 pubchem154699486
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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