Main compound image
ritonavir metabolite m5
  • Other Name: Ritonavir metabolite M5
  • InChIKey: OMGKCSSVWSHTFS-UHFFFAOYSA-N
  • InChI: InChI=1S/C32H45N5O4S/c1-21(2)28(36-31(40)37(5)19-25-20-42-30(35-25)32(3,4)41)29(39)34-24(16-22-12-8-6-9-13-22)18-27(38)26(33)17-23-14-10-7-11-15-23/h6-15,20-21,24,26-28,38,41H,16-19,33H2,1-5H3,(H,34,39)(H,36,40)
  • SMILES: CC(C)C(C(=O)NC(CC1=CC=CC=C1)CC(C(CC2=CC=CC=C2)N)O)NC(=O)N(C)CC3=CSC(=N3)C(C)(C)O
  • Exact Mass: 595.31923
  • Molecular Formula: C32H45N5O4S
  • Compound CID: pubchemlite169502032 pubchem169502032
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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