Main compound image
atazanavir metabolite m11
  • Other Name: Atazanavir metabolite M11
  • InChIKey: LUVXXTGCDNWEOD-LNNKYLDISA-N
  • InChI: InChI=1S/C38H50N6O9/c1-37(2,3)31(41-35(50)52-5)34(49)43-44(21-26-15-17-27(18-16-26)28-14-10-11-19-39-28)22-30(47)29(20-25-12-8-7-9-13-25)40-33(48)32(42-36(51)53-6)38(4,23-45)24-46/h7-19,22,29,31-32,45-47H,20-21,23-24H2,1-6H3,(H,40,48)(H,41,50)(H,42,51)(H,43,49)/b30-22-/t29-,31+,32+/m0/s1
  • SMILES: CC(C)(C)[C@@H](C(=O)NN(CC1=CC=C(C=C1)C2=CC=CC=N2)/C=C(/[C@H](CC3=CC=CC=C3)NC(=O)[C@H](C(C)(CO)CO)NC(=O)OC)\O)NC(=O)OC
  • Exact Mass: 734.36393
  • Molecular Formula: C38H50N6O9
  • Compound CID: pubchemlite169501982 pubchem169501982
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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