Main compound image
ranolazine metabolite rs-88250-glucuronide
  • Other Name: Ranolazine metabolite RS-88250-glucuronide
  • InChIKey: TUDVBUSEXFXICH-BCHVZBRRSA-N
  • InChI: InChI=1S/C20H29N3O8/c1-10-7-12(30-20-17(27)15(25)16(26)18(31-20)19(28)29)8-11(2)14(10)22-13(24)9-23-5-3-21-4-6-23/h7-8,15-18,20-21,25-27H,3-6,9H2,1-2H3,(H,22,24)(H,28,29)/t15-,16-,17+,18-,20?/m0/s1
  • SMILES: CC1=CC(=CC(=C1NC(=O)CN2CCNCC2)C)OC3[C@@H]([C@H]([C@@H]([C@H](O3)C(=O)O)O)O)O
  • Exact Mass: 439.19546
  • Molecular Formula: C20H29N3O8
  • Compound CID: pubchemlite169502142 pubchem169502142
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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