Main compound image
(2s,4s)-4-(4-(pyrimidin-2-yl)piperazin-1-yl)pyrrolidine-2-carboxylic acid
  • Other Name: L-Proline, 4-(4-(2-pyrimidinyl)-1-piperazinyl)-, (4S)-
  • InChIKey: XIVLJKIXZCUOQB-QWRGUYRKSA-N
  • InChI: InChI=1S/C13H19N5O2/c19-12(20)11-8-10(9-16-11)17-4-6-18(7-5-17)13-14-2-1-3-15-13/h1-3,10-11,16H,4-9H2,(H,19,20)/t10-,11-/m0/s1
  • SMILES: C1CN(CCN1[C@H]2C[C@H](NC2)C(=O)O)C3=NC=CC=N3
  • Exact Mass: 277.15387
  • Molecular Formula: C13H19N5O2
  • Compound CID: pubchemlite118753184 pubchem118753184
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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