Main compound image
ritonavir_m5
  • Other Name: (2S)-N-[(2S,4S,5S)-5-amino-4-hydroxy-1,6-diphenylhexan-2-yl]-2-[[[2-(2-hydroxypropan-2-yl)-1,3-thiazol-4-yl]methyl-methylcarbamoyl]amino]-3-methylbutanamide
  • InChIKey: OMGKCSSVWSHTFS-VNNZRSTGSA-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)/t24-,26-,27-,28-/m0/s1
  • SMILES: CC(C)[C@@H](C(=O)N[C@@H](CC1=CC=CC=C1)C[C@@H]([C@H](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: pubchemlite118753567 pubchem118753567
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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