Main compound image
lopinavir m6/m7/m8 metabolite(s)
  • Other Name: Lopinavir M6/M7/M8 metabolite(s)
  • InChIKey: HTQFODBBXMZHPJ-JKAXMSHYSA-N
  • InChI: InChI=1S/C37H48N4O6/c1-24(2)34(41-19-9-18-38-37(41)46)36(45)39-29(20-28-14-16-30(42)17-15-28)22-32(43)31(21-27-12-6-5-7-13-27)40-33(44)23-47-35-25(3)10-8-11-26(35)4/h5-8,10-17,24,29,31-32,34,42-43H,9,18-23H2,1-4H3,(H,38,46)(H,39,45)(H,40,44)/t29-,31-,32-,34-/m0/s1
  • SMILES: CC1=C(C(=CC=C1)C)OCC(=O)N[C@@H](CC2=CC=CC=C2)[C@H](C[C@H](CC3=CC=C(C=C3)O)NC(=O)[C@H](C(C)C)N4CCCNC4=O)O
  • Exact Mass: 644.35739
  • Molecular Formula: C37H48N4O6
  • Compound CID: pubchemlite169501901 pubchem169501901
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.

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