Main compound image
chembl3706524
  • Other Name: (2S)-N-[(2S)-1,1-dihydroxy-3-phenylpropan-2-yl]-2-(quinoline-2-carbonylamino)butanediamide
  • InChIKey: JWWYNZOXGNSUHE-OALUTQOASA-N
  • InChI: InChI=1S/C23H24N4O5/c24-20(28)13-18(22(30)27-19(23(31)32)12-14-6-2-1-3-7-14)26-21(29)17-11-10-15-8-4-5-9-16(15)25-17/h1-11,18-19,23,31-32H,12-13H2,(H2,24,28)(H,26,29)(H,27,30)/t18-,19-/m0/s1
  • SMILES: C1=CC=C(C=C1)C[C@@H](C(O)O)NC(=O)[C@H](CC(=O)N)NC(=O)C2=NC3=CC=CC=C3C=C2
  • Exact Mass: 436.17467
  • Molecular Formula: C23H24N4O5
  • Compound CID: pubchemlite122197279 pubchem122197279
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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