Main compound image
lamivudine-sulfoxide
  • Other Name: 5-(2-Hydroxy-4-iminopyrimidin-1(4H)-yl)-2-(hydroxymethyl)-1,3lambda~4~-oxathiolan-3-one
  • InChIKey: LJMQAXFNQNADRZ-FYZWQCAOSA-N
  • InChI: InChI=1S/C8H11N3O4S/c9-5-1-2-11(8(13)10-5)6-4-16(14)7(3-12)15-6/h1-2,6-7,12H,3-4H2,(H2,9,10,13)/t6-,7+,16?/m1/s1
  • SMILES: C1[C@@H](O[C@@H](S1=O)CO)N2C=CC(=NC2=O)N
  • Exact Mass: 245.04703
  • Molecular Formula: C8H11N3O4S
  • Compound CID: pubchemlite452020 pubchem452020
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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