Main compound image
raltegravir-sulfate (m2)
  • Other Name: Raltegravir-sulfate (M2)
  • InChIKey: ORYYOUAZQBZZQM-UHFFFAOYSA-N
  • InChI: InChI=1S/C20H21FN6O8S/c1-10-25-26-17(34-10)16(29)24-20(2,3)19-23-13(14(18(30)27(19)4)35-36(31,32)33)15(28)22-9-11-5-7-12(21)8-6-11/h5-8H,9H2,1-4H3,(H,22,28)(H,24,29)(H,31,32,33)
  • SMILES: CC1=NN=C(O1)C(=O)NC(C)(C)C2=NC(=C(C(=O)N2C)OS(=O)(=O)O)C(=O)NCC3=CC=C(C=C3)F
  • Exact Mass: 524.11256
  • Molecular Formula: C20H21FN6O8S
  • Compound CID: pubchemlite169502038 pubchem169502038
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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